Tumor-stromal crosstalk in pancreatic cancer and tissue fibrosis

The tumor microenvironment of pancreatic cancer: Altered extracellular matrix alliances fibrosis and cancer

The tissue microenvironment comprises an active population of cellular and non-cellular components that forms an organized niche to regulate the homeostasis of any organ [17, 18]. Over the past few decades, significant understanding has been achieved in identifying several oncogenes and tumor suppressor genes in pancreatic cancer. These genes regulate cell growth, inflammation, apoptosis, and multifaceted signaling networks [19, 20]. For instance, in pancreatic cancer, Kras mutations are predominant and drive tumorigenesis. Several other genes, such as CDKN2A, TP53 and SMAD4, participate in the progression of cancer. Accumulation of such mutations in the normal cell drive it to a benign tumor state and stays dormant while it lacks the ability to invade and metastasize other parts and form vasculature [21, 22]. A very large body of evidence suggests the involvement of aforementioned genes and tumor microenvironments contributing to PC progression. However, the mechanism of tumor microenvironment mediated progression of pancreatic cancer remains elusive.

How tumor cells communicate with external signals from neighboring cells are what make it so perilous, and we must address the fact that tumor expansion greatly depends on its microenvironment. The tumor microenvironment consists of not only tumor cells, but also other cell types such as fibroblasts, immune cells (T & B Cells, NK cells, Tumor associated macrophages), blood vessels, ECM and other signaling molecules [23, 24]. The cellular and non-cellular components in the microenvironment maintain tissue homeostasis and play a pivotal role in opposing resistance to malignant cell growth [25]. Three different types of normal cells in the tumor microenvironment have been identified: stromal cells, fibroblasts, and immune cells. Cellular cross-talk between cancer and stromal cells is critical for cancer progression [26]. Fibroblasts and stromal cells secrete growth factors, such as fibroblast growth factor (FGF), to mediate tumor progression. Apart from tumor progression and support to malignant cells, these cell types function as chemoattractant that instigate migration of other cells to the microenvironment. The pancreatic tumor microenvironment consists of abundant stromal cells, especially pancreatic stellate cells [27], and tumor stroma possess dual signals of tumor suppression and promotion. For instance, inhibition of Hedgehog signaling reduced the abundance of stroma and improved vascular delivery of the anticancer agent, gemcitabine [28, 29]. ECM is yet another major factor in the progression of PDAC. ECM contains proteins such as laminin, fibronectin, proteoglycans, glycoproteins, and polysaccharides, with diverse physical and biochemical properties. Collagens are the most abundant matrix proteins; wherein pancreatic tissue undergoes both synthetic and degradative processes. Furthermore, collagen architecture needs to be maintained in normal homeostasis. Any abrupt change in the deposition of collagens results in tissue fibrosis, thereby limiting tissue function [30, 31]. Cancer-associated fibroblasts (CAFs) are vital components of the tumor microenvironment involved in the stromal-to-tumor interaction [32].

An orchestrated crosstalk between mutated cells and the microenvironment leads to altered ECM composition and results in activation of resident fibroblasts and recruitment of inflammatory cells and pericytes, thereby promoting angiogenesis and cancer progression (Fig. 1). It is worthwhile to address: a. the specific signals that cancer cells transmit and receive from their environment; and b. how the received signals initiate a malignant growth. Recently, using the emerging orthotopic tumor model, which mimics the effects of tumor microenvironments, rather than ectopic transplantation models, a connection was reported of the pancreatic tumor microenvironment and associated cells [33]. Nevertheless, these questions remain unanswered, but further attempts to understand these findings will, we believe open the way toward developing a novel strategy to inhibit PDAC progression.

Fibrosis in pancreatic ductal adenocarcinoma

A dense fibrotic stroma or desmoplasia, comprises excessive production of ECM and proliferation of stromal cells, is found with both chronic pancreatitis and PDAC. The replacement of normal parenchyma with a desmoplastic environment results in exocrine and endocrine inefficiency of pancreas and is one of the important pathophysiological hallmarks of PDAC. Of interest, when compared with other solid tumors, PDAC is reported to have the highest amount of stroma [34]. The desmoplasia imposes a high burden during radiotherapy, given that it is very difficult to discriminate between tumor growth and fibrotic stroma. Desmoplastic reaction is characterized by fibrillar proteins, glycoproteins, proliferating fibroblasts, inflammatory cytokines, and immune cells. This desmoplastic reaction in PDAC is responsible for increased drug resistance [35]. Several signaling cascades that affect tumor epithelial and stromal compartments have been reported to play critical role in the pathogenesis of PDAC in connection with fibrotic responses. While Kras mutation is an early event in tumorigenesis that occurs in the pancreatic epithelial compartment, transforming growth factor (TGF)-β signaling is known as a dual compartment signaling cascade with a prominent function in the epithelial and stromal compartments [36]. The composition of fibrogenic mediators in pancreatic fibrosis was demonstrated in a TGF-β over-expressed transgenic mouse model, and the level of collagen I and III were increased initially, followed by increased deposition of fibronectin, fibroblast growth factors, and pancreatic stellate cells. Furthermore, pancreatic ECM machinery is mainly regulated through TGF-β signaling [37]. Recently, a research group reported that TGF-β within the stromal compartment of the pancreas directly participates in cancer progression and metastasis, using a monoclonal antibody, G28, which neutralizes the activity of murine TGF-βII. The resulting decreased activation of fibroblasts and collagen deposition when using G28 strongly support the significance of TGF-β-mediated desmoplastic reaction during pancreatic cancer progression [38]. An interesting and significant role of TGF-β as a tumor suppressor in the early stage of PDAC, through promotion of apoptosis and cell cycle arrest at the G1 phase, has also been reported [39, 40], and the function of TGF-β signaling in PDAC appears to be complex. However, it has been more evidently demonstrated that the decisive role of the tumor microenvironment obtains in the action of TGF-β as a tumor suppressor or promoter. Pancreatic stellate cells in the stromal compartment are responsible for excess matrix production, and, being a potent activator of stellate cells, TGF- β accelerates the metastasis of cancer cells in the stromal region [41]. Altered expression of TGF- β in the pancreatic stroma results in the dysregulated turnover of ECM and leads to aberrant accumulation of matrix proteins and immune cells, which further creates a favorable environment for invasion and metastasis of cancer cells.

Fibrogenesis in the pancreas itself is a complex process which occurs due to multiple factors, such as external injury to the tissue, chronic pancreatitis, and aberrant cell death. Such tissue injury activates the release of several inflammatory cytokines, chemokines, and growth factors to the site of injury [42]. These growth factors, including TGF-β, vascular endothelial growth factor (VEGF), platelet derived growth factor (PDGF), angiotensin, and others, activate pancreatic stellate cells that facilitate the accumulation of myofibroblasts. The proliferation of fibroblasts and conversion of fibroblasts to myofibroblasts are the key events responsible for the excessive deposition of ECM proteins, particularly collagen [43, 44]. The resulting collagen-rich meshwork creates a favorable environment for survival and proliferation of cancer cells [45]. In addition to TGF-β, other signaling pathways such as VEGF and PDGF also play important roles in triggering desmoplastic reaction in the stromal compartment of the pancreas [46, 47]. External or internal injury to the epithelial cells, as well as activated pancreatic stellate cells, are also shown to activate cell proliferation by undergoing epithelial-to-mesenchymal transition (EMT), a mechanism which further links fibrosis and cancer metastasis [48] (Fig. 2). Interestingly, parallel biological reactions controlled by the same set of molecules are involved in pancreatic fibrosis and cancer progression. It is hoped that, the increasing evidence of fibroblasts and stromal elements in the pancreas will lead to a paradigm shift in the treatment modalities of pancreatic cancer.

Pancreatic stellate cells as sprouted seeds for tumor progression

Although active research in pancreatic cancer is ongoing, it has yet to develop a targeted therapy and has failed to prolong the survival of patients with PDAC. This situation demands more research focus on the infrastructure of tumor, so called stroma, as it is believed that desmoplastic reactions and fibrotic stroma protect the cancer cell as a barrier from chemotherapy [49]. Activated pancreatic stellate cells (PSCs) in the stroma, present as a quiescent or inactive form in normal pancreatic tissue, are considered as the sprouted seed of cancer progression and metastasis. Although as early as 1876, the star-shaped lipid containing cells was initially identified in the liver [50], the first description of these cells in the pancreas was not made until 1982 [51]. In the parenchyma of normal pancreas, PSCs exist in an inactivated form that contains abundant vitamin A and fat droplets in its cytoplasm. Loss of lipid droplets by any physiological or pathological reactions results in the activation of PSCs, which show increased expression of α-smooth muscle actin (α-SMA) and desmin and fibroblast-like features [52]. PSCs are highly responsible for the aberrant secretion of matrix proteins such as collagen, laminin, and fibronectin in the ECM that induces desmoplastic reactions in the pancreas [53, 54]. The normal function of PSCs in the healthy pancreas includes immune reaction, phagocytosis, and stimulation of amylase secretion from the pancreas [55]. However, tumorigenesis induces conformational change in PSCs, which then exhibit myofibroblast-like characteristics and have a strong effect upon tumor progression and metastasis. Fibroblast-like cells expressing α-SMA, collagen I and III, laminin, and fibronectin have been identified in the fibrotic area in pancreatic cancer tissue by electron microscopy and immunofluorescence analysis [56]. As the balance regulator in ECM by way of secreting matrix metalloproteases and tissue inhibitors of matrix metalloproteases, PSCs highly contribute to fibrotic formation in the pancreas. These cells also stimulate angiogenesis and facilitate the invasion and extravasation of cancer cells. A fluorescent, in situ hybridization study revealed that human PSCs accompany cancer cells to various metastatic sites and facilitate intravasation and extravasation of cells from the blood vessel [57]. PSCs also promote EMT, which is seen by the decreased expression of epithelial marker E-cadherin and increased expression of mesenchymal markers such as N-cadherin, vimentin, and transcriptional factor Snail [31]. PSCs are highly activated in hypoxic condition, and, since pancreatic cancers are hypovascular, PSCs are believed to be the triggering factor for cancer cell invasion and metastasis [58]. In this view, PSCs act as the sprouting seed for progression of the tumor tree, with much evidence pointing to its crucial role in inducing fibrotic environment that facilitates cancer metastasis.

Blood coagulation cascade, hypoxia and wound healing: The seed bomb of tumor progression

It is interesting to discuss the interrelationship between cancer progression and the blood coagulation cascade, wound healing machinery, and fibrotic reactions. This cross-connection between these biological phenomena was identified over a century ago, when Dvorak called cancer ‘wounds that do not heal’ [59]. Cancer usually develops at the site of chronic tissue injury [60], where tissue reactions in response to injury accompany inflammatory reactions, cell proliferation, and tissue re-modeling. In addition, the adequate formation of a hemostatic clot is crucial in healing of normal injury and tissue repair. From this point of view, it is very difficult to separate the blood coagulation cascade from the wound repairing mechanisms [61]. Several research studies support tumorigenesis upon chronic injury to the respective tissues. For example, epidemiological studies show that the risk factor for developing pancreatic cancer is 18.5-fold higher in patients with chronic pancreatitis compared to people with normal pancreas [62]. Further, the critical influence of the coagulation cascade in the inflammatory and fibro-proliferative reactions followed by tissue injury has been extensively studied [63]. Upon injury, injured tissue is covered by a new epithelial layer, which is promoted by the combined action of hematopoietic clot formation, fibroblasts proliferation, and the action of inflammatory cytokines and growth factors. Highly activated platelets are recruited to the site of injury, where serum fibrinogen influences fibrin clot formation, and this reaction induces the formation of new blood vessels. During these mechanisms, activated fibroblasts migrate to the wound bed and stimulate secretion of collagen [64]. However, this collective action can enhance the risk of tumorigenesis in tissues when excessive, and therefore aberrant wound healing can be considered as an initiation event of pancreatic cancer development.

Interestingly, environmental alterations strongly facilitate aberrant wound healing and tissue scar formation; one such key determinant of the tumor microenvironment is tissue oxygenation. Following tissue injury, the compromised blood vessel function leads to a hypoxic state which is sustained further due to the high oxygen demand for the influx of inflammatory cytokines and chemokines [65]. Hypoxia induces several changes in cancer cell metabolism that results in the physiochemical changes in the tumor microenvironment such as reduced pH and increased production of ROS. Similarly, hypoxia promote molecular changes also in normal and cancerous cells by eventually activating the transcription factor hypoxia-inducible factors (HIF) [66]. Hypoxia induced events in the tumor microenvironment are mainly regulated by HIF. Upon tissue injury, the circulation of angiogenic cells such as endothelial precursor cells and mesenchymal stem cells for the appropriate angiogenic responses and wound contraction are mediated through HIF. Consequently, reduced activity of HIF-1α is sufficient to impair wound healing process that results in tissue scar formation [67]. Overexpression of HIF-1α correlates to the activation of pancreatic stellate cells through macrophage recruitment which is critical for the development of desmoplasia has been reported [68]. Hypoxic state induces the production of cytokines and chemokines such as CCL2 and its hematopoietic cell receptor CC chemokine receptor 2 (CCR2), VEGF-1, chemokine (C-X3-C motif) receptor 1 (CX3CR1) to attract macrophages and monocytes in the microenvironment. Interaction between these macrophages and pancreatic stellate cells promote the formation of dense desmoplasia around the tumor [69]. Macrophages are functioning in the activation of stellate cells through the production of several growth factors (TGF-β1, PDGF, fibroblast growth factor-2), cytokines (TNF-α, IL-1, IL-6) and chemokines. CCL2 is a classical chemokine that is highly expressed in the hypoxia region; however, its expression and the severity of hypoxia is still controversial. A research group has reported that hypoxia significantly inhibits the production of CCL2 by macrophages and negatively regulates the macrophage infiltration in pathological tissues [70]. In contrast to this, HIF 1-α promoted the secretion of CCL2 to recruit macrophages which facilitate the formation of pancreatic fibrosis during PDAC progression has also been reported [68]. Promoter region of CCL2 contains hypoxia response elements (HREs) which can bind HIF-1 further support the regulation of CCL2 function by hypoxia [71]. Notably, CCL2 is believed to be the most specific cytokine during monocyte and macrophage recruitment to the wound site. However, other C-C binding proteins such as CCL5 and macrophage inflammatory protein-1 are considered as dispensable for wound repairing mechanisms [72]. Hypoxia promote the production of large amount of CCL2 which is 30 times higher than secreted under normal condition [73]. An impaired macrophage invasion and delayed wound healing in CCL2-null mice effectively demonstrate its importance in wound repairing machinery [74]. Together, both early and late stage of normal wound healing, starting from the angiogenic response, cellular infiltrations, and fibroblasts proliferation to tissue growth and remodeling, is about connected to hypoxia. Targeting hypoxia and angiogenic responses likely to improve the current clinical management of fibrotic conditions during PDAC progression. Yet another hypothesis suggests that repeated injury to pancreatic tissue and regeneration to repair damaged epithelium increases the possibility for somatic mutations. One study reported that chronic pancreatitis in adult mice leads to pancreatic cancer with a mutation in Kras oncogene [75]. Cells with mutated DNA support the initiation and development of desmoplastic reactions in the site of injury and facilitate cancer metastasis through the induction of EMT [76]. However, future studies are warranted to obtain a clearer of the mechanisms of the wound healing machinery and how hypoxia and angiogenic response influence it to induce desmoplastic reactions and thereby tumor progression in the pancreas.

Chronic inflammation fertilizes tumor progression

In 1863, Rudolf Virchow and his group observed the presence of leukocytes in neoplastic tissue and reported for the first time the possibility of tumorigenesis in areas of chronic inflammation [77]. The immune system and immune response reactions are necessary to maintain healthy surveillance of normal tissues. The escape of unbridled tumor cells within this machinery and upon malignant transformation leads to the creation of a pro-tumorigenic environment [78]. During the early generation of tumor cells in a tissue, immune cells, particularly T cells, detect danger signals from transformed cancerous cells, and in turn initiates immune reactions to eliminate the tumor cells. Hiroaka et al. have reported the anti-tumor response of immune surveillance reactions in the initial intraepithelial phase of human PDAC [79]. However, abundant infiltration of immune cells along with inflammatory cytokines fertilizes the tumor microenvironment. The growth factors, cytokines, and angiogenic mediator-releasing ability of stromal cells in the pancreatic desmoplastic region influences tumor growth to a greater extent [80].

Increased T cell infiltration at the tumor margin has been demonstrated in a genetically engineered mouse model of pancreatic cancer. The exhaustion of T cells from one state to a differential state induces the up-regulation of inhibitory receptors. The development of a special class of antibody checkpoint inhibitors against this T-cell exhaustion provides new hope to overcome drug resistance in PDAC [81]. In yet another study, it has been demonstrated that leukocyte infiltration, regulatory T cells, and tumor-associated macrophages were dominant in the early phase of tumor progression and persisted in invasive stages of tumors in a genetically defined mouse model of PDAC [82]. It has been reported that independent of sex, age, and geographic location, the risk of cancer development is significantly high in patients with chronic pancreatitis, as shown in a study of 2015 human subjects [83]. In a mouse model of PDAC, it was reported that blockade of toll-like receptor (TLR) protects against tumorigenesis through NF-κB, MAPK pathway [84]. Ruxolitinib, a Janus kinase 1 (JAK1)/JAK2 inhibitor, along with capecitabine, is in phase III clinical trials against advanced progression of metastatic pancreatic cancer [85]. Yet another important signaling pathway activated by inflammatory reaction in the pancreas is TGF-β. Aoyagi et al. have reported that overexpression of TGF-β enhances the level of type I and III collagen, and that the mRNA expression of TGF-β, fibroblast growth factor, platelet-derived growth factor A and C, and epidermal growth factor were significantly higher in surgical cancer nodules of pancreatic cancer patients [86]. All these signaling transcription factors further facilitate the secretion of inflammatory cells and thus create a favorable microenvironment with growth factors, reactive oxygen species, and inflammatory cells that have the potential to proliferate tumor cells. These pathological factors potentiate tumor growth by inducing more proliferation of fibroblasts in the desmoplasia, greater stimulation of angiogenesis, and further enabling of metastatic spread of tumors to distant organs. In this way, the journey of tumor cells from tumorigenesis to metastasis is fertilized by inflammation and fibrotic reactions.

Extracellular matrix: The fertile soil for tumor progression

The extra cellular matrix (ECM) is a complex network of macromolecules that provides a physical scaffold to maintain tissue architecture. ECM not only provides structural foundation but generates various biochemical signals that regulate cellular behavior and function [87]. ECM plays a major role in tumor progression, given that it compasses 70% of the tumor microenvironment. All the proteins, glycoproteins, and polysaccharide components of ECM are generally produced by epithelial and stromal cells whose purpose is to separate the epithelial compartment from the stromal compartment. Collagen, laminin, and fibronectin meshwork form the basement membrane [88]. The altered organization and enhanced post-translational modification of matrix proteins results in the induction of desmoplasia (Fig. 3); and this fibrotic area accounts for 90% of the tumor area in the pancreas [89]. The tumorigenic functions of major proteins in the ECM is discussed in Table 1. In fact, the frequency and features of the tumor are designed by the stromal cells that surround it. This hypothesis is strongly supported by the findings of Hwang et al., who have reported that co-injection of pancreatic tumor cells (BxPC3 and Panc1) along with human PSCs in an orthotopic model of pancreatic cancer resulted in increased tumor size and metastasis, all of which are directly proportional with the volume of human PSCs [90]. Kamphorst et al. have reported yet another interesting role of ECM during PDAC progression. The levels of metabolomic parameters, such as glucose, glutamine, serine, creatine phosphate, and upper glycolytic intermediates are very low in tumor tissue compared with neighboring tissue. However, the group has observed an accumulation of essential amino acids in the tumor tissue. Their findings suggest that accumulation of essential amino acids could arise from degradation of extracellular proteins through macropinocytosis [91]. This study was supported by yet another recent work, which showed protein catabolism and macropinocytosis by in situ PDAC cells [92]. They have reported that when there is a lack of glucose or glutamine, the amino acid proline, derived from ECM, acts as a readily available substrate to help tumor cells to compensate for the metabolic challenge [93]. In this way, ECM can be considered to readily facilitate the growth and survival of tumor cells.

ECM proteins	Function	Ref
Type 1 collagen	Maintain the invasive phenotype of tumor cells; contributes to drug resistance in PDAC cells by increasing the expression of membrane type 1-MMP which potentiates integrin signaling.	[128, 129]
Hyaluronan	Enhance cell proliferation, metastasis and angiogenesis by interacting with CD44 and receptor for HA-mediated motility (RHAMM)	[130, 131]
Fibronectin	Promote tumor cell survival through increase ROS; Enhancing tumor cell migration through promoting FAK-dependent activation of Rho	[132, 133]
Laminin	Promote metastasis through the formation of hemidesmosomes; cleaved laminin stimulates motility of epithelial cells	[134]
Cytokeratin	Regulate cancer cell growth and motility through modulation of PI3K/Akt signaling	[135, 136]
Osteopontin	Contribute to chemoresistance towards Gemcitabine treatment via activation of NF-κB pathway	[137]
Thrombospondin-1	Facilitate tumor cell motility and metastasis through the up-regulation of matrix metalloprotease 9	[138]
Periostin	Promote cell proliferation, migration and invasion of pancreatic cancer cells	[139]
Versican	Facilitate tumor cell growth and angiogenesis	[140]
Tenascin C	Enhances tumor cell motility through the activation of integrin signaling	[141]

Epithelial-to-mesenchymal transition facilitates branching out of cancer metastasis

Epithelial-to-mesenchymal transition (EMT) is a well-composed biological program that functions in the framework of embryogenesis, wound healing and repair mechanisms, and cancer metastasis, that drives epithelial cells toward a mesenchymal cell state. Type 1 EMT allows epithelial cells to attain the features of mesenchymal cells with the potential to form secondary epithelia by undergoing the reverse mechanism, called mesenchymal-epithelial transition (MET). Type 1 EMT mainly operates in the context of embryogenesis and organ formation. Type 2 EMT is strongly associated with tissue regeneration, wound healing, and fibrotic machinery. Cancerous cells undergoing type 3 EMT which allow the cells to invade the blood stream and generate cancerous nodules in distant organs, and thereby facilitate metastasis [94]. During EMT, epithelial cells lose their characteristic sheet-like structure by losing cell adherens and tight junction molecules, and acquire mesenchymal features with spindle-shape morphology, migratory capacity, and invasiveness [95]. Cell adherent molecules such as E-cadherin and integrins, and tight junction molecules such as occludenes and claudins, are the major epithelial markers. N-cadherin, Snail, slug, fibronectin, and vimentin are the observed mesenchymal markers [96]. There has been a tremendous increase in recent research trends to monitor the cadherin switch from E-cadherin to N-cadherin as a marker for studying cancer metastasis [97]. Another interesting aspect of EMT phenomena is that of the partial EMT, wherein epithelial cells lose E-cadherin and do not switch to express N-cadherin. This results in an intermediate phase, and this hybrid phenotype is thought to enhance migratory properties and thereby generate circulating tumor cells [98].

EMT associated with pancreatic cancer metastasis has been highly influenced by several secretory factors, including TGF-β, PDGF, and VEGF in tumor stroma. TGF-β interacts with other growth factors to stimulate the malignant transformation of epithelial and stromal cells, and activates the proliferation of cancer-associated fibroblasts, thereby inducing fibrotic conditions in the stroma. By this mechanism, pancreatic fibrosis and cancer meet together in the stromal compartment of the pancreas [99, 100]. The plasticity of newly transformed mesenchymal cells from epithelial cells is regulated by various epigenetic factors. The circulating tumor cells are highly ‘metastable,’ with the potential to undergo EMT to form mesenchymal cells or to reverse the mechanism (Fig. 4) [101]. Other than epigenetic factors, several other environmental factors also affect induction of EMT in PDAC. Very recently, Chen et al. reported that hypoxia is a major factor in determining whether the cancerous cells undergo EMT or MET in pancreatic cancerous tissue. BxPc-3 and Panc-1 cells grown under hypoxic conditions showed an increased induction of partial EMT, increased migratory capacity, and invasiveness. Administration of specific inhibitors to HIF1-α significantly reversed these changes in cancer cells [102]. The pro-apoptotic protein Par-4 is reported to have the ability to regulate E-cadherin expression by modulating the promoter activity of transcriptional factor twist and induces MET in metastatic pancreatic cancer cells [103]. Yet another deleterious pathological role of EMT in PDAC is drug resistance [104, 105], in which cancer cells avoid the effects of drugs with the aid of EMT and stem cell properties. The dissemination and stemness of cancerous cells are crucial for the progression of PDAC, therefore a better understanding of how EMT relates to metastasis in PDAC provides new possibilities for diagnostic and therapeutic treatment especially for the metastatic stages of PDAC.

Drug resistance in pancreatic cancer

Drug resistance in cancer imposes a frustrating problem in cancer therapy. Many cancers are vulnerable to chemotherapy; however, over a certain period, cells develop resistance through mutations in DNA and metabolic changes, and thereafter inhibiting drug effectiveness or showing lack of response [106]. Cancer drug resistance is caused by drug inactivation, aberrant drug efflux, altered DNA repair mechanism, inhibition of cell death, altered EMT, epigenetic factors, or a combination of these processes. Drug resistance in tumor cells exhibits cancer recurrence. Overall, the mechanisms of cancer drug resistance are still not completely understood, though the involvement of multiple signaling pathways have been reported [107, 108]. Many chemotherapeutic drugs, including Gemcitabine, Pimasertib, the Folfirinox regimen (5-fluorouracil [5-FU], irinotecan, oxaliplatin and leucovorin), and Abraxane have been proposed for pancreatic cancer [109–111], and recent reports of the mechanisms of chemoresistance in pancreatic cancer are reviewed [112].

Gemcitabine (2′,2′-difluoro – 2’deoxycytidine), for example, is a deoxycytidine analog and the first line of drugs conventionally used for pancreatic cancer patients. Gemcitabine incorporates replicating DNA and inhibits synthesis of DNA. Gemcitabine uptake is facilitated by nuclear transporters (hENT1), and once inside cells, deoxycytidine kinase (dCK) is the first enzyme involved in the phosphorylation cascade, where it facilitates activation of gemcitabine into gemcitabine di and triphosphates, mediating its cytotoxicity [113]. The metabolites of gemcitabine inhibit other key enzymes, such as cytidine triphosphate synthetase, and deoxycytidine monophosphate deaminase [114]. Compared to other anticancer drugs, pancreatic cells exhibit more susceptibility towards gemcitabine treatment, and its use also enhances the quality of life factors for patients. However, the major drawback reported is that survival is prolonged for just one month [115]. Nevertheless, certain other regimens with the potential to improve the clinical efficiency of gemcitabine have also been documented [116]. Combination therapy with gemcitabine has given inconsistent results in clinical trials, and therefore extensive studies are warranted.

Current clinical trials targeting tumor-stroma in pancreatic cancer

Chemical compounds and combinations designed to target the specific desmoplastic features of pancreatic cancer offer new avenues for the development of stromal-based therapies. Manipulation of the tumor stromal compartments help in depriving cancer cells without affecting normal tissue functions. Together, these clinical approaches could offer significant insights into tumor-stroma interactions which is pivotal in tumor progression and could lead to the development of novel cancer associated desmoplasia-targeting agents for the treatment of pancreatic cancer.