Skip to main content
Download PDF

Exosomal noncoding RNAs in Glioma: biological functions and potential clinical applications

Molecular Cancer volume 19, Article number: 66 (2020) Cite this article

Abstract

Gliomas are complex and heterogeneous brain tumors with poor prognosis. Glioma cells can communicate with their surroundings to create a tumor-permissive microenvironment. Exosomes represent a new means of intercellular communication by delivering various bioactive molecules, including proteins, lipids and nucleic acids, and participate in tumor initiation and progression. Noncoding RNAs (ncRNAs) including microRNA, long-noncoding RNA, and circular RNA, account for a large portion of human transcriptome and play important roles in various pathophysiological processes, especially in cancers. In addition, ncRNAs can be selectively packaged, secreted and transferred between cells in exosomes and modulate numerous hallmarks of glioma, such as proliferation, invasion, angiogenesis, immune-escape, and treatment resistance. Hence, the strategies of specifically targeting exosomal ncRNAs could be attractive therapeutic options. Exosomes are able to cross the blood brain barrier (BBB), and are readily accessible in nearly all types of human biofluids, which make them the promising biomarkers for gliomas. Additionally, given the biocompatibility of exosomes, they can be engineered to deliver therapeutic factors, such as RNA, proteins and drugs, to target cells for therapeutic applications. Here, we reviewed current research on the roles of exosomal ncRNAs in glioma progression. We also discussed their potential clinical applications as novel biomarkers and therapeutics.

Introduction

Glioma is the most common and malignant primary tumor of the central nervous system (CNS). Glioblastoma (GBM), the most lethal glioma, accounts for 70% of all diffuse glioma diagnoses and has a median overall survival of 15 months [1]. Currently, standard GBM treatments include maximal safe surgical resection and combined radio-chemotherapy [2]. Apart from the rapid proliferation, extensive invasion, intra- and inter-tumoral genetic heterogeneity, and treatment resistance of GBM, the dismal prognosis of GBM patients also originates from poor understanding of molecular pathogenesis and lacking of timely diagnosis and sensitive therapeutic monitoring tools [3]. Therefore, it is crucial to elucidate molecular mechanisms underlying glioma development and progression, and further explore reliable biomarkers.

Glioma is a complex and heterogeneous tumor. It not only contains tumor cells, but also has many kinds of nontumoral cell types, such as astrocytes, microglia, endothelial cells and immune cells, which together constitute the complex glioma microenvironment [4]. Increasing evidence revealed that communication between tumor cells and the surrounding components in the glioma microenvironment may directly affect various hallmark features of glioma [4, 5]. For example, tumor cells can change the nonneoplastic astrocytes phenotype by the glioma microenvironment, which in turn promotes glioma growth and invasion [6]. In addition, tumor cells have the ability to survive in the local microenvironment, and eventually changing it to their own advantage via multiple types of cell-cell communication [7]. Elucidating the mechanisms by which glioma cells interact with the tumor microenvironment can uncover multiple potential therapeutic targets for clinical applications. Tumor cells can communicate with neighboring or distant cells through a variety of ways, either by direct cell interactions through membrane receptors and their ligands, or by releasing soluble factors, such as cytokines, chemokines, and metabolites [8]. Recently, exosomes, as a new means of intercellular communication, have drawn much attention due to their ability to carry various bioactive molecules that modulate the activities of recipient cells [9, 10] (Fig. 1a). Among these bioactive compositions, noncoding RNAs (ncRNAs) are enriched and stable in exosomes, and have attracted substantial attention due to their regulatory function in the initiation and progression of various cancers [11]. In this review, we summarized current research on the roles of exosomal ncRNAs in glioma progression as well as their potential clinical applications.

Fig. 1
figure 1

Roles of exosomes in glioma. a exosomes participate in cell-to-cell communication by delivering various bioactive molecules, including proteins, lipids and nucleic acids, in the tumor microenvironment. b exosomes serve as promising biomarkers. c exosomes have novel therapeutic applications

Full size image

Biogenesis and characteristics of exosome

Exosomes, 40–150 nm in diameter, are endosome-derived, small extracellular vesicles (EVs) secreted by a wide variety of cells, which exist in almost all body fluids, including blood, cerebrospinal fluid (CSF), urine, saliva and breast milk [12, 13]. The secretory quantity of exosomes and their contents can vary according to their biogenesis, cell of origin and cell’s status. Studies have shown that some molecules are enriched in exosomes while others are barely present, suggesting a selective sorting feature [14]. The biogenesis of exosome begins at endosome formation through endocytosis at the plasma membrane, and then early endosomes maturate to multivesicular endosomes (MVEs). Exosomes are generated within the endosomal system as intraluminal vesicles (ILVs), which formed by the inward budding of the limiting membrane of MVEs [13] (Fig. 2a). The biogenesis of exosome involves a series of sequential molecular machineries, and the most important one is the endosomal sorting complexes required for transport (ESCRT) machinery, which plays essentially role in the formation of ILVs and MVEs as a driver of membrane shaping and scission [13, 15]. The ESCRT system comprises ESCRT-0, −I, −II, and -III, which act in a stepwise manner wherein ESCRT-0 and ESCRT-I participate in cargo clustering and recruitment of ubiquitylated transmembrane cargoes, ESCRT-II takes charge of initiating the inward budding process, and ESCRT-III perform budding and fission of vesicles. The proteins syntenin and ALIX (the ESCRT accessory protein ALG-2 interacting protein X) can intersect with the ESCRT pathway, which regulates the process of exosome biogenesis [16] (Fig. 2b). In addition, several studies suggest that exosomes can still be formed despite the depletion of ESCRT complexes, suggesting the existence of an ESCRT-independent pathway [17]. Tetraspanins, specifically CD9, CD63 and CD81, are reported to play important roles in the ESCRT-independent endosomal sorting [13, 18]. Thus, both the ESCRT-dependent and -independent pathways are implicated in exosome biogenesis, and their role and contribution may vary depending on the specific cargoes and cell types. Generally, the MVEs either fuse with the lysosome for degradation or fuse with plasma membrane, which secretes the ILVs (exosomes) into the extracellular space (Fig. 2a). Like its biogenesis, exosome release also involves several crucial factors and the Rab GTPase family, such as Rab27a and Rab27b, are involved in the trafficking of MVBs to a specific cell membrane region [19]. After secretion, exosomes interact with neighboring or distant recipient cells through several ways, including ligand/receptor interaction, direct membrane fusion and endocytosis, to modulate the activities of recipient cells [20].

Fig. 2
figure 2

The main process of exosome biogenesis and release. a The biogenesis of exosome begins at endosome formation through endocytosis at the plasma membrane, and then early endosomes maturate to multivesicular bodies (MVB). Exosomes are formed as intraluminal vesicles (ILV) in MVBs though endosomal sorting complexes required for transport (ESCRT) dependent or independent pathway. Generally, MVBs either fuse with the lysosome for degradation or fuse with the plasma membrane, which results in ILVs (exosomes) secretion. After secretion, exosomes uptake by target cells is mediated by endocytosis, fusion with the plasma membrane or ligand/receptor interaction. b Both the ESCRT- dependent and independent pathway are implicated in controlling the cargos sorting of exosomes

Full size image

The release of exosome into extracellular environment was initially assumed to be a means of eliminating unneeded materials in cells and its biological significance was ignored for a long time [21]. However, extensive research now suggests that exosomes are critical mediators for cell-to-cell communication and involved in the pathogenesis of many diseases, including cancers [22, 23]. Tumor-derived exosomes can change the behavior of surrounding stromal cells, which ultimately create a suitable microenvironment for tumor growth [24]. Meanwhile, stromal cells in the tumor microenvironment can in turn affect tumor progression through the release of exosomes [25,26,27,28,29,30]. Thus, the complex interactions between tumor and stromal cells via exosomes in local or distant microenvironments promote proliferation, invasion, angiogenesis, immune-escape, metastases and treatment resistance [31]. Furthermore, there is growing interest in the potential clinical application of exosome, with a focus on biomarkers of disease and therapeutic delivery vehicles [12] (Fig. 1b and c).

Noncoding RNAs in exosome

A variety of molecules have been identified in exosomes, including proteins, lipids and nucleic acids [32]. The double-layer membranes of exosome protect these molecules from proteases, nucleases, and other environmental impacts [33]. Besides, these molecules in exosomes are selectively packaged, secreted and transferred between cells, and are highly variable depending upon the parental cells and pathophysiological conditions [34]. Increasing evidence has shown that exosomes are enriched with ncRNAs, including microRNA (miRNAs), long-noncoding RNA (lncRNA), circular RNA (circRNA), piwi-interacting RNAs (piRNAs) and tRNA-derived small noncoding RNA (tsRNA), which play important roles in various pathophysiological processes, especially in cancers [35,36,37,38]. With the discovery of ncRNAs in exosomes and further research, many new functions and applications have emerged, from new ways of cell-to-cell communication to promising disease biomarkers and, given the biocompatibility of exosomes, possibly novel therapeutic applications. In this review, we mainly focused on the exosomal miRNAs, lncRNAs, and circRNAs in glioma.

MicroRNA

MiRNAs are small ncRNAs consisting of approximately 21–25 nucleotides, which act as regulators of gene expression by complementary binding of targeted mRNA’s 3′ untranslated regions (UTR), thus reducing the stability or inhibiting translation of target genes [39] (Fig. 3b). Each miRNA may have multiple target mRNAs, and one mRNA may be targeted by several miRNAs, thus leading to a complex regulatory network. The biogenesis of miRNA begins with transcribing miRNA gene into large primary transcript (pri-miRNA), and it is then cleaved into a ~ 85-nucleotide stem–loop structure called precursor miRNA (pre-miRNA) by the microprocessor complex including the type III RNase Drosha and the RNA-binding protein DGCR8. The pre-miRNA is then processed to a ~ 20–22-nucleotide miRNA/miRNA duplex by the RNase III enzyme Dicer. These miRNA duplexes are unstable and soon are cleaved into single stranded mature miRNAs. The mature miRNA is loaded onto an Argonaute protein (AGO) to form the RNA induced silencing complex (RISC), which then binds to target mRNA for post-transcriptional gene silencing [39] (Fig. 3a). Currently, the latest release of the miRBase database (v22) contains 1917 annotated hairpin precursors, and 2654 mature miRNAs in the human genome [40]. Numerous studies have indicated that dysregulation of miRNA expression is closely associated with many human diseases, including cancers. MiRNAs may play oncogenic roles or function as tumor suppressors under certain conditions [41]. Recently, the discovery of miRNAs in exosomes gained increasing attention. Extensive studies suggest that miRNAs are selectively sorted into exosomes that participate in cell-to-cell communication in the tumor microenvironment and play an essential part in tumor biology [5]. Furthermore, the easy access, abundance and stability of exosomal miRNAs in biofluids have made them ideal biomarkers for various types of cancers, including gliomas [42].

Fig. 3
figure 3

The biogenesis (a) and potential functions (b) of miRNA, lncRNA and circRNA

Full size image

Long-noncoding RNA

LncRNAs are defined as transcripts longer than 200 nucleotides in length that have no or limited protein-coding capacity [43]. LncRNAs exist in either the nucleus or cytoplasm, and play distinct functions depend on their subcellular localizations. In the nucleus, lncRNAs may participate in transcriptional regulation of gene expression and mRNA splicing. While in the cytoplasm, they could affect mRNA stability and regulate protein function [44]. Moreover, lncRNAs exert their functions through multiple molecular mechanisms, such as binding with DNA to modulate gene transcription, acting as the competing endogenous RNA (ceRNA) or miRNA sponges to regulate gene expression at post-transcriptional level, associating with proteins, and encoding functional small peptides [45] (Fig. 3b). Over the last decade, it has been increasingly demonstrated that lncRNAs are involve in many pathophysiological processes, such as cell cycle regulation, cell differentiation, and innate immune response [45, 46]. Furthermore, dysregulation of lncRNAs expression has been observed in many human cancers, including gliomas, and is closely related to the stage and grade of cancers through their roles as tumor suppressors or oncogenes [43]. Interestingly, lncRNAs can also be selectively sorted into exosomes and contribute to intercellular communication in the tumor microenvironment [47]. Exosomal lncRNAs can participate in the onset and progression of gliomas, such as proliferation, invasion, angiogenesis and drug resistance, which may act as attractive therapeutic targets [6, 48, 49]. Furthermore, exosomal lncRNAs have potential for diagnostic and prognostic biomarkers [47].

Circular RNA

CircRNAs, a novel class of endogenous ncRNAs with a closed loop structure, are primarily produced from pre-mRNAs via back-splicing [50] (Fig. 3a). CircRNAs were initially thought to be byproducts of RNA splicing. Recently, researchers show great interests in the properties and functions of circRNAs because of the discovery of more circRNAs with important functions [51]. Furthermore, circRNAs exhibit tissue- and developmental stage-specific expression, and their expression is often independent of related linear isoforms [52]. Currently, several studies have demonstrated that circRNA expression is most abundant in the brain compared with other tissues, implying their important roles in brain function and brain diseases [53]. Though the exact functions of most circRNAs remain unclear, accumulating evidence suggests that circRNAs may regulate gene expression at multiple levels, such as regulating transcription of their parental genes, affecting splicing of their linear cognates, acting as miRNA sponges, regulating the function of RNA-binding proteins, and encoding peptides [52, 54] (Fig. 3b). CircRNAs are reported to participate in various physiological and pathological processes, particularly in cancers [51, 55]. Many studies have shown that circRNAs are aberrantly expressed in cancer including gliomas and play a vital role in tumor initiation and progression [56, 57].

Recently, the presence of circRNAs, in addition to miRNAs and lncRNAs, has also been detected in exosomes by Li and colleagues in 2015 [58]. Research on exosomal circRNAs is still at an initial stage, but a small number of studies suggest that circRNAs are enriched in exosomes, through which circRNAs start their circulation and reach the recipient cells, thus carrying out their various biological functions [58, 59]. Unlike linear RNAs, circRNAs with loop structure are much more stable and have a longer half-life, therefore, making them more suitable for developing biomarkers than the linear RNA transcripts [57, 60].

The functional roles of exosomal ncRNAs in glioma

As the most common and deadly primary brain tumors, gliomas typically exhibit as rapid proliferation and extensive invasion, immune surveillance escape, angiogenesis induction, and drug resistant. However, their underlying molecular mechanisms remain unclear yet. Emerging evidence suggests that exosomes mediate glioma initiation and progression through transferring bioactive molecules between different cell populations [61]. As one of important contents, exosomal ncRNAs play key roles in multi-aspects of tumor biology, including proliferation, invasion, angiogenesis, immune-escape, metastases and treatment resistance within the tumor microenvironment [11]. In the following sections, we summarized the current research on the specific roles and mechanisms of exosomal ncRNAs in glioma progression (Table 1).

Table 1 The biological functions of exosomal ncRNAs in glioma
Full size table

Exosomal ncRNAs and cell proliferation/invasion in glioma

Rapid proliferation and extensive invasion are the most important hallmarks of malignant gliomas, which involve in complex molecular pathways and dynamic crosstalk between tumor cells and microenvironment. These growth features may ultimately lead to the incomplete surgical resection and inevitable tumor recurrence [80]. Hence, identifying the key molecules that associate with tumor proliferation and invasion is critical to devising new treatment strategies. Increasing evidence shows that ncRNAs play important roles in glioma progression [35]. Glioma-derived exosomes carrying a broad range of ncRNAs are reported to exert significant functions in glioma proliferation and invasion through regulating intercellular communication in local and distant microenvironments [6, 48, 63,64,65, 71] (Fig. 4a).

Fig. 4
figure 4

Exosomal ncRNAs play important roles in regulating glioma proliferation/invasion (a), angiogenesis (b), immune-escape (c), and treatment resistance (d)

Full size image

Certain miRNAs are selectively packaged into exosomes and regulate cell proliferation and invasion in glioma [65, 66]. MiR-1 is known as a tumor suppressor in several cancers [81]. Bronisz et al. found that miR-1 could be transferred by GBM–derived EVs to the surrounding GBM cells, and reduced GBM growth and invasion through directly targeting the expression of Annexin A2 (ANXA2), an important pro-oncogenic factor in GBM [65]. Another study by Cai et al. observed an increased level of exosomal miR-148a in GBM patient’s serum when comparing to healthy volunteers. Moreover, miR-148a delivered by exosomes promotes GBM cell proliferation and metastasis via targeting cell adhesion molecule 1 (CADM1) to enhance STAT3 signaling activity. CADM1 was proved to be a tumor suppressor which was downregulated in glioma tissues and most glioma cell lines [63].

Besides miRNAs, some exosomal lncRNAs, such as lncRNA-ATB [6] and lncRNA-AHIF [48], were reported to regulate cell proliferation and invasion in glioma. Bian and colleagues found that glioma cell-derived exosomes had the ability to shuttle lncRNA-ATB to astrocytes and promoted the activation of astrocytes, which could in turn promote the invasion and migration of glioma cells. More importantly, lncRNA-ATB activats astrocytes through the suppression of miR-204-3p in an Argonaute 2 (Ago2)-dependent manner [6]. Taken together, these studies suggest that ncRNAs selectively secreted and transferred between cells in exosomes play important roles in regulating glioma proliferation and invasion.

Exosomal ncRNAs and glioma angiogenesis

As a crucial hallmark of blood vessel-rich tumors, angiogenesis plays a significant role in the development and progression of gliomas, especially the GBM [82]. Tumor angiogenesis is a complex process comprising multiple steps, such as degradation of basement membrane, endothelial cell proliferation, migration, sprouting, branching, and tube formation, and depending on the coordination of many regulators [83, 84]. Vascular supply is the fundamental requirement for proliferation and invasion of glioma, for rapid growth of tumor requires even more nutrients and oxygen supply. As relevant studies demonstrated that solid tumors can’t grow larger than 2–3 mm in diameter without inducing their own blood supply [85]. The mechanism underlying angiogenesis is not entirely clear. Aberrant activation of the HIF-1α/VEGF pathway can induce endothelial cell proliferation and migration, which is considered to be one of the underlying causes of angiogenesis [86]. Therefore, a better understanding of the cellular and molecular mechanisms involved in tumor angiogenesis will be required for developing novel anti-angiogenic therapies.

Extensive studies have revealed that ncRNAs play important regulatory roles in tumor angiogenesis [84]. In the tumor microenvironment, exosomes released by different cell types, such as tumor cells, mesenchymal stem cells and stromal cells, can be captured by endothelial cells that encourage growth of new blood vessels [68,69,70]. Increasing evidence suggests that exosomes exert the function of angiogenesis regulation partly by delivering ncRNAs in the glioma microenvironment [49, 67,68,69,70,71] (Fig. 4b). As an oncomiR, miR-21 is expressed in a wide range of cancers, and regulates many biological processes [75]. Sun et al. found that glioma stem cells-derived exosomes carrying miR-21 could promote the angiogenic ability of endothelial cells through upregulating VEGF expression, which further interacting with VEGFR2 to activate downstream PI3-kinase/Akt pathway [70]. Furthermore, Chen and colleagues revealed that miR-9 could be secreted from glioma cells via exosomes and was then absorbed by vascular endothelial cells. MiR-9 could target PHD3, which mediated HIF-1α/VEGF signaling pathway to increase glioma angiogenesis. This study suggested miR-9 could be treated as a potential therapeutic target for glioma [71]. There are many exosomal lncRNAs, such as lncRNA-HOTAIR, lincRNA-CCAT2 and lincRNA-POU3F3, that have been confirmed to play crucial roles in the regulation of glioma angiogenesis [49, 67, 68]. For instance, the lncRNA-HOTAIR, a well-characterized oncogene in various cancers, including gliomas, is associated with tumor proliferation, migration and invasion, and its expression is closely associated with glioma grades [87]. Ma et al. found that HOTAIR can be secreted by glioma cells via exosomes and delivered to endothelial cells, thus promoting glioma angiogenesis though regulation of VEGF expression [49]. Similarly, another study by Lang et al. revealed that glioma cells could transfer linc-CCAT2 to endothelial cells by exosomes to activate VEGFA and TGFβ, and thereby promoting angiogenesis [67].

Glioma stem cells (GSCs) are a small minority of the cancer cell population that show multipotent glioma-initiating capacity [88]. Increasing evidence suggests that GSCs are found in close association with vascular niches [89], while blood vessels support GSCs, and these stem cells in turn may regulate and contribute to the glioma angiogenesis through various ways, including the secretion of exosomes. Wang et al. also found GSCs could release exosomes that mediate cellular communication by delivering miRNAs. The results showed that GSCs-derived exosomes overexpressing miR-26a contributed to enhanced proliferation and angiogenesis of human brain microvascular endothelial cells in vitro through specifically binding to PTEN, which further regulated the PI3K/Akt signaling pathway in glioma [69]. These studies suggested that GSCs can promote the angiogenic ability of endothelial cells via exosomal ncRNAs.

Exosomal ncRNAs and immunosuppressive microenvironment

As a substantial part of the glioma microenvironment, glioma-associated immune cells have an emerging role in tumor progression and in controlling anti-tumor immune responses [4, 90]. Bone marrow-derived macrophages, along with the resident CNS microglia, can constitute up to 30% of the tumor mass, which exert pro-tumorigenic functions and creat an immunosuppressive microenvironment [4, 91]. Glioma cells can shape the immune cells via exosomes, thus creating an optimum microenvironment for tumor survival and growth [23, 61]. Glioma-associated microglia and macrophages are key drivers of the local immunosuppression promoting tumor progression and its resistance to immunomodulating therapeutic strategies [92]. Hence, targeting these immune cells and related moleculars represents a novel promising treatment strategy for glioma patients.

Recent studies revealed that glioma cells derived exosomal ncRNAs, such as miR-451 [24], miR-1246 [74] and miR-21 [75], could change the phenotype of microglia and macrophages to promote glioma growth and survival (Fig. 4c). Van der Vos and colleagues investigated exosomal miRNA released from glioma cells and taken up by microglia and macrophages as a means by which tumor cells manipulate normal cells in glioma microenvironment [24]. They further monitored phenotypic changes in microglia exposed to isolated GBM derived EVs in culture, as well as their effects on target mRNAs in an intracranial mouse glioma model. Their results showed that high levels of miR-451/miR-21 were transferred from glioma cells to microglia via EVs with a decrease of a common mRNA target encoding c-Myc, which led to increased microglia proliferation and shifting of cytokine profile toward immune suppression [24]. Myeloid-derived suppressor cells (MDSCs) play an important role in mediating the formation of an immunosuppressive environment and assisting gliomas in evading the host immune response, but the specific mechanisms have not been clearly defined. Guo et al. isolated normoxia-stimulated and hypoxia-stimulated glioma-derived exosomes, which could be taken up by MDSCs, and studied their MDSC induction abilities in vivo and in vitro. The authors found that hypoxia- stimulated glioma-derived exosomes had a stronger ability to induce MDSCs, and it was the hypoxia-inducible expression of exosomal miR-10a and miR-21 that mediated MDSC differentiation and activation by targeting RAR-related orphan receptor alpha (RORA) and phosphatase and tensin homolog (PTEN) [72]. In another study by the same authors found glioma exosomal miR-29a/miR-92a could also mediate the formation of immunosuppressive microenvironment via enhancing the proliferation and differentiation of functional MDSCs by targeting high-mobility group box transcription factor 1 (Hbp1) and protein kinase cAMP-dependent type I regulatory subunit alpha (Prkar1a), respectively [73]. These studies suggest that glioma can influence the differentiation and activation of MDSCs via exosomal miRNAs, thus affecting the entirety of tumor immune environment.

Exosomal ncRNAs and treatment resistance

For high-grade gliomas, radiotherapy and chemotherapy after maximum safe resection have always been the cornerstone of treatment [2]. However, it’s reported that high-grade gliomas, especially GBM, tend to exhibit advanced resistance to multiple anti-tumor therapeutic methods [93]. Radio- and chemoresistance in glioma are major factors affecting the effectiveness of treatment and leading to poor prognosis. There is compelling evidence that GSCs are resistant to radiation and chemotherapy, and thereby form the basis for glioma recurrence [94]. In recent years, accumulating evidences suggest that exosomes, as an important communicator of intercellular communication, may led to horizontal propagation of resistance capacity between heterogeneous populations of cancer cells, and ultimately blocking the successful treatment of many cancers [11, 14]. In addition, recent studies revealed that ncRNAs delivered by exosomes play important roles in promoting tumor cell adaptation to the tumor microenvironment and treatment resistance [62, 95] (Fig. 4d). Thus, exploring the mechanism of treatment resistance can be extremely significant in order to eradicate these incurable tumors.

As a monofunctional DNA-alkylating agent, temozolomide (TMZ) is used as a first-line chemotherapy in glioma through inducing DNA damage in glioma cells [96]. TMZ resistance limits the durability of the treatment response and affects the prognosis of patients. Relevant studies suggest that TMZ-resistant glioma cell-derived exosomes can transfer TMZ chemoresistance to recipient TMZ-sensitive cells via exosomes [76, 77]. Zhang et al. found that lncRNA SBF2-AS1 showed upregulated expression in TMZ-resistant GBM cells and glioma tissues, and was associated with TMZ resistance. Meanwhile, exosomal could transfer lncRNA SBF2-AS1 from chemoresistant GBM cells to chemoresponsive GBM cells to spread TMZ resistance. Further study revealed lncRNA SBF2-AS1 functioned as a ceRNA and could regulate the expression of X-ray repair cross complementing 4 (XRCC4) by sponging miR-151a-3p, thus promoting the repair process of TMZ-induced DNA damage [77].

Exosomal ncRNAs released by glioma cells can also interfere with the sensitivity to radiotherapy and thus affect the treatment efficiency. Yang et al. reported that exosomal miR-301a specifically secreted by hypoxic GBM cells could transfer to corresponding normoxia-cultured cells and promote radiation resistance by targeting TCEAL7 genes [79]. In addition, a recent study demonstrated that circRNA-ATP8B4 from radioresistant GBM derived EVs could also promote glioma radioresistance by sponging miR-766 [78]. Therefore, these exosomal ncRNAs harbor a great therapeutic significance as promising agents for future clinical applications either independently or complementary to modulate radio- and chemoresistance in glioma treatment.

Potential clinical applications of exosomal ncRNAs in glioma

Exosomal ncRNAs serve as promising biomarkers

Nowadays, advanced neuroimaging, such as magnetic resonance imaging (MRI), is the principal diagnostic method for patients with suspected brain lesions. Although neuroimaging may suggest glioma diagnosis, other brain lesions might share quite similar radiological features, which makes it difficult for differential diagnosis [97]. Furthermore, it is often difficult to distinguish true radiographic progression from pseudoprogression in the postoperative follow-up [98]. Moreover, the commonly used high-resolution MRI, which by the way, isn’t very high resolution compared to histology examination. The lowest MRI resolution ranges on the order of millimeters, whereas the dimensions of the tumor cell are in micrometers [99], this disparity in scale may lead to delay in diagnosis and treatment. Histological examination of the tumor tissue obtained by biopsy or surgery is currently the golden standard for definite diagnosis. However, these practices may be associated with significant morbidity, and repeated sampling of tumor tissue is not always appropriate. Besides, biopsies may not reflect the heterogeneity of gliomas due to the small amounts of tissue samples. As mentioned earlier, TMZ is used as a first-line chemotherapy in high-grade glioma after maximum safe resection [96]. TMZ resistance limits the durability of the treatment response. Hence, it will be important to monitor TMZ resistance in biofluids for adjusting treatments. Above all, developing of minimal invasive methods, for the detection, differentiation and monitoring of gliomas will be clinically meaningful, especially in those patients in which surgery is contraindicated or biopsy results are inconclusive.

Although conventional strategies for liquid biopsies have been shown to be promising, it remains a huge challenge to develop clinically validated tumor detection biomarkers, especially for gliomas. At present, biomarkers which have been studied extensively, including circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), circulating proteins, and EVs [100]. With the perspective of various types of circulating biomarkers, the primary concern is how representative they are of the whole tumor, or at least they can reflect the primary biological features of the tumor. Ideally, CTCs could enable profiling of the whole-tumor genome, however the number of CTCs is too small to detect, and can only reflect a single cell type of the heterogeneous tumor. Furthermore, the ctDNA contains the mutations present in tumor and seems to be much more abundant than CTCs, but it also fails to reflect tumor heterogeneity. Whereas, exosomes contain a variety of functional molecules that can reflect the complex heterogeneity of the whole tumor. And, best of all, they are extremely stable and are readily accessible in nearly all types of human biofluids [101]. These factors make exosomes the most promising biomarkers.

An increasing number of studies have evidenced key roles of ncRNAs in the initiation and progression of various cancers, including gliomas [102]. In addition, ncRNAs are secreted into the circulation either circulate freely or be selectively packaged into exosomes, suggesting these molecules can be used as new biomarkers. The double-layer lipid membrane of exosomes can protect ncRNAs from the ribonuclease-mediated degradation. In addition, previous research has suggested that exosomes can cross the blood brain barrier (BBB) [103]. Hence, the exosomal ncRNAs have a good clinical application prospect in glioma diagnosis and caused more and more attention [104,105,106,107,108] (Table 2).

Table 2 The biomarker potential of exosomal ncRNAs in glioma
Full size table

CSF examination has been widely used in clinical practice for monitoring of CNS diseases but is less used in gliomas to date. Previous studies suggested that the miR-21 expression in glioma was up-regulated, and the levels of miR-21 were also correlated with the histological grade [110, 111]. Hence, miR-21 has drawn great attentions for its potential as diagnostic and prognostic biomarkers. Akers et al. found that the CSF EV miR-21 levels from GBM patients were, on average, ten-fold higher than that isolated from controls, which suggested CSF EV miR-21 may serve as a diagnostic biomarker for GBM patients [109]. A similar study by shi et al. also found that exosomal miR-21 levels in the CSF of glioma patients were significantly higher than in the controls. Interestingly, the results showed no difference in serum-derived exosomal miR-21 expression. In addition, CSF exosomal miR-21 levels were correlated with tumor recurrence and spinal/ventricle metastasis [110]. These studies suggest CSF-derived exosomal ncRNAs could be used as promising biomarkers for glioma diagnosis and prognosis.

Another important source of glioma biomarker is blood. Yang et al. found that the miR-221 expression level was increased in high-grade glioma tissue, and further analysis revealed a significant higher serum exosomal miR-221 level in glioma patients than in controls. More importantly, exosomal miR-221 level in serum increased with the glioma grades [62]. This study suggests that exosomal miR-221 may serve as a novel diagnostic biomarker for glioma patients. Information about long-term prognosis of glioma patients may assist identification of patients requiring special attention. With the increased availability of various types of predictive biomarkers, a non-invasive, rapid and highly sensitive biomarker that can evaluate the patient’s prognosis is clinically meaningful. Recent work has shown that exosomal ncRNAs may serve as independent prognostic parameters for gliomas [105]. Lan and colleagues found that an increased serum exosomal miR-301a level was associated with a longer overall survival (OS). And further Cox regression analyses verified serum exosomal miR-301a level was independently associated with patient’s OS [105]. Acquired drug resistance is a major constraining factor in clinical treatment of glioma. Thus, identifying the underlying drug resistant patients and finding alternative methods of treatment timely are extremely important to improve prognosis. Zhang et al. found that higher serum exosomal lncRNA SBF2-AS1 levels from recurrent GBM patients were associated with worse prognosis and poorer response to TMZ treatment [77]. In conclusion, these studies suggest that exosomal ncRNAs in biofluids have shown great potential in biomarker development, and their clinical applications deserve further research.

The potential application of exosomal ncRNAs in anti-glioma therapy

Considering the important biological functions of exosomal ncRNAs in gliomas, the strategies of specifically targeting exosomes or their cargoes, such as the ncRNAs, can be promising therapeutic options in the treatment of gliomas. Hence, many ongoing studies are designed either to modulate exosomes production or block exosomes uptake pathways so as to achieve the goal of treating cancer [112]. One study proposed a novel device strategy that allowed rapid extracorporeal capture and selective retention of target particles < 200 nm from the entire circulatory system using an affinity plasmapheresis platform known as the Aethlon ADAPTTM (adaptive dialysis-like affinity platform technology) system, which can be used to incorporate diverse affinity agents for capturing cancer-specific exosomes on the basis of displaying surface proteins or glycoproteins [113]. The safety and effectiveness of this strategy are supported by clinical experience in hepatitis C virus (HCV)-infected patients using an ADAPTTM device to reduce the systemic load of virions, which have similar sizes and glycosylated surfaces as cancer-derived exosomes [113, 114]. Therefore, the concept of reducing circulating cancer-specific exosomes could offer a unique treatment for cancer patients. NcRNAs, such as miRNAs, lncRNAs and circRNAs, are important regulatory molecules in the initiation and development of gliomas, and play crucial roles in almost every aspect of biological processes, including tumor proliferation\invasion, angiogenesis and treatment resistance [35]. With advances in the understanding of ncRNA function, exosomal ncRNAs will become attractive therapeutic targets for the treatment of gliomas.

The BBB helps protect the brain, but it also creates difficulties in treating neurological disorders, including gliomas [115]. As double-layer phospholipid membrane vesicles with abundant bioactive molecules inside, exosomes exhibit distinct advantages as gene therapy delivery vectors. Furthermore, exosomes have their own special features, such as small size, flexibility and good histocompatibility, which enable them to cross the major biological barriers in the body such as the BBB [103]. Lai et al. designed a highly sensitive EVs reporter system, which enables tracking of EVs biodistribution over time in vivo imaging. Through this system, they found that systemically injected EVs can be delivered to tumor sites within an hour [116]. Therefore, exosomes could be used as a promising therapeutic delivery system in glioma treatment.

As exosomes serve as natural ncRNA carriers, they may be adapted to deliver tumor suppressive ncRNAs. Generally, tumor suppressive ncRNAs are downregulated in cancer, and overexpressing these ncRNAs via exosomes in tumor cells may inhibit tumor progression. Katakowski and colleagues found that intra-tumor injection of exosomes, which were released by MSCs overexpressing miR-146b, an anti-glioma miRNA that can reduce glioma cell invasion, migration and viability, significantly reduced glioma xenograft growth in a rat model of primary brain tumor [25]. A similar study by Fareh et al. engineered primary glioma cells to stably express the miR-302-367, and this tumor suppressive miRNA was largely enclosed in exosomes, which were internalized by the neighboring GBM cells, thus inducing antitumor cell effects in vitro and in vivo [66]. Furthermore, Munoz et al. found that delivery of functional anti-miR-9 by MSCs–derived exosomes to GBM cells could make GBM sensitive to TMZ [117]. These studies suggest that exosomes could be used as vehicles for delivery of anti-tumor ncRNAs, demonstrating their potential use for therapeutic applications. In addition to transfering various ncRNAs, other types of both endogenous and exogenous therapeutic cargoes such as proteins, lipophilic small molecules and drugs, can also be loaded into these particles for cancer therapy [112]. However, a vast amount of further study is needed before these therapeutic approaches would be available for clinical application.

Conclusions and prospects

Glioma is the most common malignant intracranial tumor with poor prognosis and could be resistant to various therapies. The pathogenesis of this deadly disease is not entirely clear which may involve thousands of genes, signals and molecular components. NcRNAs including miRNA, lncRNA and circRNA, account for a large portion of human transcriptome and play indispensable roles in the glioma initiation and progression. Exosomes represent a new means of intercellular communication and are enriched with ncRNA content. Extensive studies suggest that exosomal ncRNAs are selectively packaged, secreted and transferred between cells that participate in cell-to-cell communication in the tumor microenvironment, and can modulate numerous hallmarks of glioma, such as proliferation, invasion, angiogenesis, immune-escape, and treatment resistance. In addition, the discovery that exosomes carry various bioactive molecules and can readily cross biological barriers (for example, BBB) hold great promises for clinical applications, including diagnostics and therapy.

Though promising, there is still a long way to go before the exosomal ncRNA can be used in clinical practice. Exosomes in the body fluids are often a heterogeneous population of vesicles of unknown origin. Accordingly, identifying and isolating the tumor-specific exosomes is particularly important, however, this could be hard to achieve currently, though there are multiple methods for isolation with the pros and cons of each. Furthermore, given the limited amount of genetic materials present in biofluid exosomes, the maximum use, normalization and quantitation remain urgent questions to solve. Exosomes mediate intercellular communication through specifically and selectively transferring bioactive molecules between cells. However, how molecules are synthesized and selectively packaged into exosomes is largely unknown, and further studies are needed to reveal the detail mechanisms. Exosomes could be engineered to deliver therapeutic factors, such as RNA, proteins and drugs, to target cells for therapeutic applications. But a precondition is that exosomes must be able to accurately find its target and release its cargo. However, the molecular mechanisms that target exosomes to a given cell type or tissue are far from clear. With progressively better understanding of these unknowns, we believe exosomes will become increasingly valuable agents in the diagnosis and therapy of diseases in the near future.

Availability of data and materials

Not applicable.

Abbreviations

AGO:

Argonaute protein

ALIX:

ALG-2 interacting protein X

BBB:

Blood brain barrier

CADM1:

Cell adhesion molecule 1

ceRNA:

Competing endogenous RNA

circRNA:

Circular RNA

CNS:

Central nervous system

CSF:

Cerebrospinal fluid

ctc:

Circulating tumor cell

ctDNA:

Circulating tumor DNA

ESCRT:

Endosomal sorting complexes required for transport

EV:

Extracellular vesicle

GBM:

Glioblastoma

GSC:

Glioma stem cell

ILV:

Intraluminal vesicle

lncRNA:

Long-noncoding RNA

MDSC:

Myeloid-derived suppressor cell

miRNA:

microRNA

MRI:

Magnetic resonance imaging

MVE:

Multivesicular endosome

ncRNA:

Noncoding RNA

OS:

Overall survival

piRNA:

Piwi-interacting RNA

RISC:

RNA induced silencing complex

TMZ:

Temozolomide

tsRNA:

tRNA-derived small noncoding RNA

UTR:

Untranslated regions

VEGF:

Vascular endothelial growth factor

References

  1. Molinaro AM, Taylor JW, Wiencke JK, Wrensch MR. Genetic and molecular epidemiology of adult diffuse glioma. Nat Rev Neurol. 2019;15(7):405–17.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Stupp R, Mason WP, van den Bent MJ, Weller M, Fisher B, Taphoorn MJ, et al. Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. N Engl J Med. 2005;352(10):987–96.

    Article  CAS  PubMed  Google Scholar 

  3. Alifieris C, Trafalis DT. Glioblastoma multiforme: pathogenesis and treatment. Pharmacol Ther. 2015;152:63–82.

    Article  CAS  PubMed  Google Scholar 

  4. Quail DF, Joyce JA. The microenvironmental landscape of brain tumors. Cancer Cell. 2017;31(3):326–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Godlewski J, Krichevsky AM, Johnson MD, Chiocca EA, Bronisz A. Belonging to a network--microRNAs, extracellular vesicles, and the glioblastoma microenvironment. Neuro-Oncology. 2015;17(5):652–62.

    Article  CAS  PubMed  Google Scholar 

  6. Bian EB, Chen EF, Xu YD, Yang ZH, Tang F, Ma CC, et al. Exosomal lncRNAATB activates astrocytes that promote glioma cell invasion. Int J Oncol. 2019;54(2):713–21.

    CAS  PubMed  Google Scholar 

  7. Ellert-Miklaszewska A, Pasierbinska M, Poleszak K, Kaminska B. Molecular interactions between tumor and its microenvironment in malignant gliomas. Postepy Biochem. 2018;64(2):129–40.

    Article  CAS  PubMed  Google Scholar 

  8. Chiodoni C, Di Martino MT, Zazzeroni F, Caraglia M, Donadelli M, Meschini S, et al. Cell communication and signaling: how to turn bad language into positive one. J Exp Clin Cancer Res. 2019;38(1):128.

    Article  PubMed  PubMed Central  Google Scholar 

  9. Raposo G, Stahl PD. Extracellular vesicles: a new communication paradigm? Nat Rev Mol Cell Biol. 2019;20:509–10.

    Article  CAS  PubMed  Google Scholar 

  10. Tkach M, Thery C. Communication by extracellular vesicles: where we are and where we need to go. Cell. 2016;164(6):1226–32.

    Article  CAS  PubMed  Google Scholar 

  11. Xie Y, Dang W, Zhang S, Yue W, Yang L, Zhai X, et al. The role of exosomal noncoding RNAs in cancer. Mol Cancer. 2019;18(1):37.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Jiang L, Gu Y, Du Y, Liu J. Exosomes: diagnostic biomarkers and therapeutic delivery vehicles for cancer. Mol Pharm. 2019;16(8):3333–49.

    Article  CAS  PubMed  Google Scholar 

  13. van Niel G, D'Angelo G, Raposo G. Shedding light on the cell biology of extracellular vesicles. Nat Rev Mol Cell Biol. 2018;19(4):213–28.

    Article  PubMed  CAS  Google Scholar 

  14. Sun Z, Yang S, Zhou Q, Wang G, Song J, Li Z, et al. Emerging role of exosome-derived long non-coding RNAs in tumor microenvironment. Mol Cancer. 2018;17(1):82.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  15. Hurley JH. ESCRT complexes and the biogenesis of multivesicular bodies. Curr Opin Cell Biol. 2008;20(1):4–11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Baietti MF, Zhang Z, Mortier E, Melchior A, Degeest G, Geeraerts A, et al. Syndecan-syntenin-ALIX regulates the biogenesis of exosomes. Nat Cell Biol. 2012;14(7):677–85.

    Article  CAS  PubMed  Google Scholar 

  17. Stuffers S, Sem Wegner C, Stenmark H, Brech A. Multivesicular endosome biogenesis in the absence of ESCRTs. Traffic. 2009;10(7):925–37.

    Article  CAS  PubMed  Google Scholar 

  18. Chairoungdua A, Smith DL, Pochard P, Hull M, Caplan MJ. Exosome release of beta-catenin: a novel mechanism that antagonizes Wnt signaling. J Cell Biol. 2010;190(6):1079–91.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Ostrowski M, Carmo NB, Krumeich S, Fanget I, Raposo G, Savina A, et al. Rab27a and Rab27b control different steps of the exosome secretion pathway. Nat Cell Biol. 2010;12(1):19–30.

    Article  CAS  PubMed  Google Scholar 

  20. Mulcahy LA, Pink RC, Carter DR. Routes and mechanisms of extracellular vesicle uptake. J Extracell Vesicles. 2014;4:3.

    Google Scholar 

  21. Johnstone RM, Adam M, Hammond JR, Orr L, Turbide C. Vesicle formation during reticulocyte maturation. Association of plasma membrane activities with released vesicles (exosomes). J Biol Chem. 1987;262(19):9412–20.

    CAS  PubMed  Google Scholar 

  22. Colombo M, Raposo G, Thery C. Biogenesis, secretion, and intercellular interactions of exosomes and other extracellular vesicles. Annu Rev Cell Dev Biol. 2014;30:255–89.

    Article  CAS  PubMed  Google Scholar 

  23. Chistiakov DA, Chekhonin VP. Extracellular vesicles shed by glioma cells: pathogenic role and clinical value. Tumour Biol. 2014;35(9):8425–38.

    Article  CAS  PubMed  Google Scholar 

  24. van der Vos KE, Abels ER, Zhang X, Lai C, Carrizosa E, Oakley D, et al. Directly visualized glioblastoma-derived extracellular vesicles transfer RNA to microglia/macrophages in the brain. Neuro-Oncology. 2016;18(1):58–69.

    Article  PubMed  CAS  Google Scholar 

  25. Katakowski M, Buller B, Zheng X, Lu Y, Rogers T, Osobamiro O, et al. Exosomes from marrow stromal cells expressing miR-146b inhibit glioma growth. Cancer Lett. 2013;335(1):201–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Deng SZ, Lai MF, Li YP, Xu CH, Zhang HR, Kuang JG. Human marrow stromal cells secrete microRNA-375-containing exosomes to regulate glioma progression. Cancer Gene Ther. 2019. https://doi.org/10.1038/s41417-019-0079-9.

  27. Yu L, Gui S, Liu Y, Qiu X, Zhang G, Zhang X, et al. Exosomes derived from microRNA-199a-overexpressing mesenchymal stem cells inhibit glioma progression by down-regulating AGAP2. Aging (Albany NY). 2019;11(15):5300–18.

    CAS  Google Scholar 

  28. Sharif S, Ghahremani MH, Soleimani M. Delivery of exogenous miR-124 to glioblastoma multiform cells by wharton's jelly mesenchymal stem cells decreases cell proliferation and migration, and confers chemosensitivity. Stem Cell Rev Rep. 2018;14(2):236–46.

    Article  CAS  PubMed  Google Scholar 

  29. Kim R, Lee S, Lee J, Kim M, Kim WJ, Lee HW, et al. Exosomes derived from microRNA-584 transfected mesenchymal stem cells: novel alternative therapeutic vehicles for cancer therapy. BMB Rep. 2018;51(8):406–11.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Zhang X, Zhang X, Hu S, Zheng M, Zhang J, Zhao J, et al. Identification of miRNA-7 by genome-wide analysis as a critical sensitizer for TRAIL-induced apoptosis in glioblastoma cells. Nucleic Acids Res. 2017;45(10):5930–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Lang FM, Hossain A, Gumin J, Momin EN, Shimizu Y, Ledbetter D, et al. Mesenchymal stem cells as natural biofactories for exosomes carrying miR-124a in the treatment of gliomas. Neuro-Oncology. 2018;20(3):380–90.

    Article  CAS  PubMed  Google Scholar 

  32. Jeppesen DK, Fenix AM, Franklin JL, Higginbotham JN, Zhang Q, Zimmerman LJ, et al. Reassessment of exosome composition. Cell. 2019;177(2):428–45.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. Kim KM, Abdelmohsen K, Mustapic M, Kapogiannis D, Gorospe M. RNA in extracellular vesicles. Wiley Interdiscip Rev RNA. 2017;8(4):e1413.

    Article  CAS  Google Scholar 

  34. Pegtel DM, Gould SJ. Exosomes. Annu Rev Biochem. 2019;88:487–514.

    Article  CAS  PubMed  Google Scholar 

  35. Nie JH, Li TX, Zhang XQ, Liu J. Roles of non-coding RNAs in normal human brain development, brain tumor, and neuropsychiatric disorders. Noncoding RNA. 2019;5(2):36.

    CAS  PubMed Central  Google Scholar 

  36. Zhu L, Liu X, Pu W, Peng Y. tRNA-derived small non-coding RNAs in human disease. Cancer Lett. 2018;419:1–7.

    Article  CAS  PubMed  Google Scholar 

  37. Zhu L, Li J, Gong Y, Wu Q, Tan S, Sun D, et al. Exosomal tRNA-derived small RNA as a promising biomarker for cancer diagnosis. Mol Cancer. 2019;18(1):74.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Li B, Hong J, Hong M, Wang Y, Yu T, Zang S, et al. piRNA-823 delivered by multiple myeloma-derived extracellular vesicles promoted tumorigenesis through re-educating endothelial cells in the tumor environment. Oncogene. 2019;38(26):5227–38.

    Article  CAS  PubMed  Google Scholar 

  39. Peng Y, Croce CM. The role of microRNAs in human cancer. Signal Transduct Target Ther. 2016;1:15004.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Macfarlane LA, Murphy PR. MicroRNA: biogenesis, function and role in cancer. Curr Genomics. 2010;11(7):537–61.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Kozomara A, Birgaoanu M, Griffiths-Jones S. miRBase: from microRNA sequences to function. Nucleic Acids Res. 2018;47(D1):D155–62.

    Article  PubMed Central  CAS  Google Scholar 

  42. Saadatpour L, Fadaee E, Fadaei S, Nassiri Mansour R, Mohammadi M, Mousavi SM, et al. Glioblastoma: exosome and microRNA as novel diagnosis biomarkers. Cancer Gene Ther. 2016;23(12):415–8.

    Article  CAS  PubMed  Google Scholar 

  43. Peng Z, Liu C, Wu M. New insights into long noncoding RNAs and their roles in glioma. Mol Cancer. 2018;17(1):61.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  44. Quinn JJ, Chang HY. Unique features of long non-coding RNA biogenesis and function. Nat Rev Genet. 2016;17(1):47–62.

    Article  CAS  PubMed  Google Scholar 

  45. Kopp F, Mendell JT. Functional classification and experimental dissection of long noncoding RNAs. Cell. 2018;172(3):393–407.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  46. Gou Q, Gao L, Nie X, Pu W, Zhu J, Wang Y, et al. Long noncoding RNA AB074169 inhibits cell proliferation via modulation of KHSRP-mediated CDKN1a expression in papillary thyroid carcinoma. Cancer Res. 2018;78(15):4163–74.

    Article  CAS  PubMed  Google Scholar 

  47. Wang M, Zhou L, Yu F, Zhang Y, Li P, Wang K. The functional roles of exosomal long non-coding RNAs in cancer. Cell Mol Life Sci. 2019;76(11):2059–76.

    Article  CAS  PubMed  Google Scholar 

  48. Dai X, Liao K, Zhuang Z, Chen B, Zhou Z, Zhou S, et al. AHIF promotes glioblastoma progression and radioresistance via exosomes. Int J Oncol. 2019;54(1):261–70.

    CAS  PubMed  Google Scholar 

  49. Ma X, Li Z, Li T, Zhu L, Li Z, Tian N. Long non-coding RNA HOTAIR enhances angiogenesis by induction of VEGFA expression in glioma cells and transmission to endothelial cells via glioma cell derived-extracellular vesicles. Am J Transl Res. 2017;9(11):5012–21.

    CAS  PubMed  PubMed Central  Google Scholar 

  50. Chen LL. The biogenesis and emerging roles of circular RNAs. Nat Rev Mol Cell Biol. 2016;17(4):205–11.

    Article  CAS  PubMed  Google Scholar 

  51. Shang Q, Yang Z, Jia R, Ge S. The novel roles of circRNAs in human cancer. Mol Cancer. 2019;18(1):6.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Li X, Yang L, Chen LL. The biogenesis, functions, and challenges of circular RNAs. Mol Cell. 2018;71(3):428–42.

    Article  CAS  PubMed  Google Scholar 

  53. Rybak-Wolf A, Stottmeister C, Glazar P, Jens M, Pino N, Giusti S, et al. Circular RNAs in the mammalian brain are highly abundant, conserved, and dynamically expressed. Mol Cell. 2015;58(5):870–85.

    Article  CAS  PubMed  Google Scholar 

  54. Zhang M, Zhao K, Xu X, Yang Y, Yan S, Wei P, et al. A peptide encoded by circular form of LINC-PINT suppresses oncogenic transcriptional elongation in glioblastoma. Nat Commun. 2018;9(1):4475.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  55. Liu J, Zhao K, Huang N, Zhang N. Circular RNAs and human glioma. Cancer Biol Med. 2019;16(1):11–23.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  56. Hao Z, Hu S, Liu Z, Song W, Zhao Y, Li M. Circular RNAs: functions and prospects in glioma. J Mol Neurosci. 2019;67(1):72–81.

    Article  CAS  PubMed  Google Scholar 

  57. Li Y, Zheng Q, Bao C, Li S, Guo W, Zhao J, et al. Circular RNA is enriched and stable in exosomes: a promising biomarker for cancer diagnosis. Cell Res. 2015;25(8):981–4.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  58. Wang Y, Liu J, Ma J, Sun T, Zhou Q, Wang W, et al. Exosomal circRNAs: biogenesis, effect and application in human diseases. Mol Cancer. 2019;18(1):116.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  59. Lasda E, Parker R. Circular RNAs co-precipitate with extracellular vesicles: a possible mechanism for circRNA clearance. PLoS One. 2016;11(2):e0148407.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  60. Tan S, Gou Q, Pu W, Guo C, Yang Y, Wu K, et al. Circular RNA F-circEA produced from EML4-ALK fusion gene as a novel liquid biopsy biomarker for non-small cell lung cancer. Cell Res. 2018;28(6):693–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  61. Rooj AK, Mineo M, Godlewski J. MicroRNA and extracellular vesicles in glioblastoma: small but powerful. Brain Tumor Pathol. 2016;33(2):77–88.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  62. Yang JK, Yang JP, Tong J, Jing SY, Fan B, Wang F, et al. Exosomal miR-221 targets DNM3 to induce tumor progression and temozolomide resistance in glioma. J Neuro-Oncol. 2017;131(2):255–65.

    Article  CAS  Google Scholar 

  63. Cai Q, Zhu A, Gong L. Exosomes of glioma cells deliver miR-148a to promote proliferation and metastasis of glioblastoma via targeting CADM1. Bull Cancer. 2018;105(7–8):643–51.

    Article  PubMed  Google Scholar 

  64. Figueroa J, Phillips LM, Shahar T, Hossain A, Gumin J, Kim H, et al. Exosomes from glioma-associated mesenchymal stem cells increase the tumorigenicity of glioma stem-like cells via transfer of miR-1587. Cancer Res. 2017;77(21):5808–19.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  65. Bronisz A, Wang Y, Nowicki MO, Peruzzi P, Ansari K, Ogawa D, et al. Extracellular vesicles modulate the glioblastoma microenvironment via a tumor suppression signaling network directed by miR-1. Cancer Res. 2014;74(3):738–50.

    Article  CAS  PubMed  Google Scholar 

  66. Fareh M, Almairac F, Turchi L, Burel-Vandenbos F, Paquis P, Fontaine D, et al. Cell-based therapy using miR-302-367 expressing cells represses glioblastoma growth. Cell Death Dis. 2017;8(3):e2713.

    Article  PubMed  PubMed Central  Google Scholar 

  67. Lang HL, Hu GW, Zhang B, Kuang W, Chen Y, Wu L, et al. Glioma cells enhance angiogenesis and inhibit endothelial cell apoptosis through the release of exosomes that contain long non-coding RNA CCAT2. Oncol Rep. 2017;38(2):785–98.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  68. Lang HL, Hu GW, Chen Y, Liu Y, Tu W, Lu YM, et al. Glioma cells promote angiogenesis through the release of exosomes containing long non-coding RNA POU3F3. Eur Rev Med Pharmacol Sci. 2017;21(5):959–72.

    PubMed  Google Scholar 

  69. Wang ZF, Liao F, Wu H, Dai J. Glioma stem cells-derived exosomal miR-26a promotes angiogenesis of microvessel endothelial cells in glioma. J Exp Clin Cancer Res. 2019;38(1):201.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  70. Sun X, Ma X, Wang J, Zhao Y, Wang Y, Bihl JC, et al. Glioma stem cells-derived exosomes promote the angiogenic ability of endothelial cells through miR-21/VEGF signal. Oncotarget. 2017;8(22):36137–48.

    Article  PubMed  PubMed Central  Google Scholar 

  71. Chen X, Yang F, Zhang T, Wang W, Xi W, Li Y, et al. MiR-9 promotes tumorigenesis and angiogenesis and is activated by MYC and OCT4 in human glioma. J Exp Clin Cancer Res. 2019;38(1):99.

    Article  PubMed  PubMed Central  Google Scholar 

  72. Guo X, Qiu W, Liu Q, Qian M, Wang S, Zhang Z, et al. Immunosuppressive effects of hypoxia-induced glioma exosomes through myeloid-derived suppressor cells via the miR-10a/Rora and miR-21/Pten pathways. Oncogene. 2018;37(31):4239–59.

    Article  CAS  PubMed  Google Scholar 

  73. Guo X, Qiu W, Wang J, Liu Q, Qian M, Wang S, et al. Glioma exosomes mediate the expansion and function of myeloid-derived suppressor cells through microRNA-29a/Hbp1 and microRNA-92a/Prkar1a pathways. Int J Cancer. 2019;144(12):3111–26.

    Article  CAS  PubMed  Google Scholar 

  74. Qian M, Wang S, Guo X, Wang J, Zhang Z, Qiu W, et al. Hypoxic glioma-derived exosomes deliver microRNA-1246 to induce M2 macrophage polarization by targeting TERF2IP via the STAT3 and NF-kappaB pathways. Oncogene. 2020;39(2):428–42.

    Article  CAS  PubMed  Google Scholar 

  75. Abels ER, Maas SLN, Nieland L, Wei Z, Cheah PS, Tai E, et al. Glioblastoma-associated microglia reprogramming is mediated by functional transfer of extracellular miR-21. Cell Rep. 2019;28(12):3105–19.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  76. Zeng A, Wei Z, Yan W, Yin J, Huang X, Zhou X, et al. Exosomal transfer of miR-151a enhances chemosensitivity to temozolomide in drug-resistant glioblastoma. Cancer Lett. 2018;436:10–21.

    Article  CAS  PubMed  Google Scholar 

  77. Zhang Z, Yin J, Lu C, Wei Y, Zeng A, You Y. Exosomal transfer of long non-coding RNA SBF2-AS1 enhances chemoresistance to temozolomide in glioblastoma. J Exp Clin Cancer Res. 2019;38(1):166.

    Article  PubMed  PubMed Central  Google Scholar 

  78. Zhao M, Xu J, Zhong S, Liu Y, Xiao H, Geng L, et al. Expression profiles and potential functions of circular RNAs in extracellular vesicles isolated from radioresistant glioma cells. Oncol Rep. 2019;41(3):1893–900.

    CAS  PubMed  Google Scholar 

  79. Yue X, Lan F, Xia T. Hypoxic glioma cells-secreted exosomal miR-301a activates the Wnt/β-catenin signaling and promotes radiation resistance by targeting TCEAL7. Mol Ther. 2019;27(11):1939–49.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  80. Xie Q, Mittal S, Berens ME. Targeting adaptive glioblastoma: an overview of proliferation and invasion. Neuro-Oncology. 2014;16(12):1575–84.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  81. Nohata N, Hanazawa T, Enokida H, Seki N. microRNA-1/133a and microRNA-206/133b clusters: dysregulation and functional roles in human cancers. Oncotarget. 2012;3(1):9–21.

    Article  PubMed  PubMed Central  Google Scholar 

  82. Onishi M, Ichikawa T, Kurozumi K, Date I. Angiogenesis and invasion in glioma. Brain Tumor Pathol. 2011;28(1):13–24.

    Article  CAS  PubMed  Google Scholar 

  83. Herbert SP, Stainier DY. Molecular control of endothelial cell behaviour during blood vessel morphogenesis. Nat Rev Mol Cell Biol. 2011;12(9):551–64.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Wang Y, Wang L, Chen C, Chu X. New insights into the regulatory role of microRNA in tumor angiogenesis and clinical implications. Mol Cancer. 2018;17(1):22.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  85. Yadav L, Puri N, Rastogi V, Satpute P, Sharma V. J Clin Diagn Res. 2015;9(6):Xe01–5.

    PubMed  PubMed Central  Google Scholar 

  86. Vallee A, Guillevin R, Vallee JN. Vasculogenesis and angiogenesis initiation under normoxic conditions through Wnt/beta-catenin pathway in gliomas. Rev Neurosci. 2018;29(1):71–91.

    Article  CAS  PubMed  Google Scholar 

  87. Pastori C, Kapranov P, Penas C, Peschansky V, Volmar CH, Sarkaria JN, et al. The bromodomain protein BRD4 controls HOTAIR, a long noncoding RNA essential for glioblastoma proliferation. Proc Natl Acad Sci U S A. 2015;112(27):8326–31.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  88. Lathia JD, Gallagher J, Myers JT, Li M, Vasanji A, McLendon RE, et al. Direct in vivo evidence for tumor propagation by glioblastoma cancer stem cells. PLoS One. 2011;6(9):e24807.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  89. Jhaveri N, Chen TC, Hofman FM. Tumor vasculature and glioma stem cells: contributions to glioma progression. Cancer Lett. 2016;380(2):545–51.

    Article  CAS  PubMed  Google Scholar 

  90. Gieryng A, Pszczolkowska D, Walentynowicz KA, Rajan WD, Kaminska B. Immune microenvironment of gliomas. Lab Investig. 2017;97(5):498–518.

    Article  CAS  PubMed  Google Scholar 

  91. Chen Z, Hambardzumyan D. Immune microenvironment in glioblastoma subtypes. Front Immunol. 2018;9:1004.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  92. Locarno CV, Simonelli M, Carenza C, Capucetti A, Stanzani E, Lorenzi E, et al. Role of myeloid cells in the immunosuppressive microenvironment in gliomas. Immunobiology. 2019. https://doi.org/10.1016/j.imbio.2019.10.002.

  93. Qazi MA, Vora P, Venugopal C, Sidhu SS, Moffat J, Swanton C, et al. Intratumoral heterogeneity: pathways to treatment resistance and relapse in human glioblastoma. Ann Oncol. 2017;28(7):1448–56.

    Article  CAS  PubMed  Google Scholar 

  94. Bao S, Wu Q, McLendon RE, Hao Y, Shi Q, Hjelmeland AB, et al. Glioma stem cells promote radioresistance by preferential activation of the DNA damage response. Nature. 2006;444(7120):756–60.

    Article  CAS  PubMed  Google Scholar 

  95. Fan Q, Yang L, Zhang X, Peng X, Wei S, Su D, et al. The emerging role of exosome-derived non-coding RNAs in cancer biology. Cancer Lett. 2018;414:107–15.

    Article  CAS  PubMed  Google Scholar 

  96. Yoshimoto K, Mizoguchi M, Hata N, Murata H, Hatae R, Amano T, et al. Complex DNA repair pathways as possible therapeutic targets to overcome temozolomide resistance in glioblastoma. Front Oncol. 2012;2:186.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  97. Smirniotopoulos JG, Murphy FM, Rushing EJ, Rees JH, Schroeder JW. Patterns of contrast enhancement in the brain and meninges. Radiographics. 2007;27(2):525–51.

    Article  PubMed  Google Scholar 

  98. Radbruch A, Fladt J, Kickingereder P, Wiestler B, Nowosielski M, Baumer P, et al. Pseudoprogression in patients with glioblastoma: clinical relevance despite low incidence. Neuro-Oncology. 2015;17(1):151–9.

    Article  PubMed  Google Scholar 

  99. Sorensen AG, Batchelor TT, Wen PY, Zhang WT, Jain RK. Response criteria for glioma. Nat Clin Pract Oncol. 2008;5(11):634–44.

    Article  PubMed  PubMed Central  Google Scholar 

  100. Westphal M, Lamszus K. Circulating biomarkers for gliomas. Nat Rev Neurol. 2015;11(10):556–66.

    Article  CAS  PubMed  Google Scholar 

  101. Bullock MD, Silva AM, Kanlikilicer-Unaldi P, Filant J, Rashed MH, Sood AK, et al. Exosomal non-coding RNAs: diagnostic, prognostic and therapeutic applications in cancer. Noncoding RNA. 2015;1(1):53–68.

    PubMed  PubMed Central  Google Scholar 

  102. Cech TR, Steitz JA. The noncoding RNA revolution-trashing old rules to forge new ones. Cell. 2014;157(1):77–94.

    Article  CAS  PubMed  Google Scholar 

  103. Matsumoto J, Stewart T, Banks WA, Zhang J. The transport mechanism of extracellular vesicles at the blood-brain barrier. Curr Pharm Des. 2017;23(40):6206–14.

    Article  CAS  PubMed  Google Scholar 

  104. Santangelo A, Imbruce P, Gardenghi B, Belli L, Agushi R, Tamanini A, et al. A microRNA signature from serum exosomes of patients with glioma as complementary diagnostic biomarker. J Neuro-Oncol. 2018;136(1):51–62.

    Article  CAS  Google Scholar 

  105. Lan F, Qing Q, Pan Q, Hu M, Yu H, Yue X. Serum exosomal miR-301a as a potential diagnostic and prognostic biomarker for human glioma. Cell Oncol (Dordr). 2018;41(1):25–33.

    Article  CAS  Google Scholar 

  106. Shao N, Xue L, Wang R, Luo K, Zhi F, Lan Q. miR-454-3p is an exosomal biomarker and functions as a tumor suppressor in glioma. Mol Cancer Ther. 2019;18(2):459–69.

    Article  CAS  PubMed  Google Scholar 

  107. Tan SK, Pastori C, Penas C, Komotar RJ, Ivan ME, Wahlestedt C, et al. Serum long noncoding RNA HOTAIR as a novel diagnostic and prognostic biomarker in glioblastoma multiforme. Mol Cancer. 2018;17(1):74.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  108. Manterola L, Guruceaga E, Gallego Perez-Larraya J, Gonzalez-Huarriz M, Jauregui P, Tejada S, et al. A small noncoding RNA signature found in exosomes of GBM patient serum as a diagnostic tool. Neuro-Oncology. 2014;16(4):520–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  109. Akers JC, Ramakrishnan V, Kim R, Skog J, Nakano I, Pingle S, et al. MiR-21 in the extracellular vesicles (EVs) of cerebrospinal fluid (CSF): a platform for glioblastoma biomarker development. PLoS One. 2013;8(10):e78115.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  110. Shi R, Wang PY, Li XY, Chen JX, Li Y, Zhang XZ, et al. Exosomal levels of miRNA-21 from cerebrospinal fluids associated with poor prognosis and tumor recurrence of glioma patients. Oncotarget. 2015;6(29):26971–81.

    Article  PubMed  PubMed Central  Google Scholar 

  111. Chan JA, Krichevsky AM, Kosik KS. MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells. Cancer Res. 2005;65(14):6029–33.

    Article  CAS  PubMed  Google Scholar 

  112. Rashed MH, Bayraktar E, Helal GK, Abd-Ellah MF, Amero P, Chavez-Reyes A, Rodriguez-Aguayo C, et al. Exosomes: from garbage bins to promising therapeutic targets. Int J Mol Sci. 2017;18(3):e538.

  113. Marleau AM, Chen CS, Joyce JA, Tullis RH. Exosome removal as a therapeutic adjuvant in cancer. J Transl Med. 2012;10:134.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  114. Tullis RH, Duffin RP, Handley HH, Sodhi P, Menon J, Joyce JA, et al. Reduction of hepatitis C virus using lectin affinity plasmapheresis in dialysis patients. Blood Purif. 2009;27(1):64–9.

    Article  CAS  PubMed  Google Scholar 

  115. Nair KGS, Ramaiyan V, Sukumaran SK. Enhancement of drug permeability across blood brain barrier using nanoparticles in meningitis. Inflammopharmacology. 2018;26(3):675–84.

    Article  CAS  PubMed  Google Scholar 

  116. Lai CP, Mardini O, Ericsson M, Prabhakar S, Maguire C, Chen JW, et al. Dynamic biodistribution of extracellular vesicles in vivo using a multimodal imaging reporter. ACS Nano. 2014;8(1):483–94.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  117. Munoz JL, Bliss SA, Greco SJ, Ramkissoon SH, Ligon KL, Rameshwar P. Delivery of functional anti-miR-9 by mesenchymal stem cell-derived exosomes to glioblastoma multiforme cells conferred chemosensitivity. Mol Ther Nucleic Acids. 2013;2:e126.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

Download references

Acknowledgements

 The figures were created with BioRender.com, and we really appreciate it.

Funding

This work was supported by grants from Fundamental Research Funds for the Central Universities (2018SCUH0018 to Y.P.), Department of Sichuan Science & Technology Program (2019JDTD0013 to Y.P.), and The 1.3.5 Project for Disciplines of Excellence, West China Hospital, Sichuan University (ZYJC18030 to Y.P.), China Postdoctoral Science Foundation (2019 M663514 to J.C.), and Post-Doctor Research Project, West China Hospital, Sichuan University (2019HXBH084 to J.C.).

Author information

Author notes

  1. Jian Cheng and Jinli Meng contributed equally to this work.

Authors and Affiliations

  1. Laboratory of Molecular Oncology, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, 610041, China

    Jian Cheng, Lei Zhu & Yong Peng

  2. Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, China

    Jian Cheng

  3. Department of Radiology, Hospital of Chengdu Office of People’s Government of Tibetan Autonomous Region (Hospital C.T.), Chengdu, China

    Jinli Meng

Authors
  1. Jian Cheng
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jinli Meng
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Lei Zhu
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Yong Peng
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

YP and JC conceived the structure of manuscript and revised the manuscript; JC and JM drafted initial manuscript; LZ revised manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Yong Peng.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Cheng, J., Meng, J., Zhu, L. et al. Exosomal noncoding RNAs in Glioma: biological functions and potential clinical applications. Mol Cancer 19, 66 (2020). https://doi.org/10.1186/s12943-020-01189-3

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12943-020-01189-3

Keywords

Molecular Cancer

ISSN: 1476-4598