- Open Access
Downregulation of ASPP2 in pancreatic cancer cells contributes to increased resistance to gemcitabine through autophagy activation
Molecular Cancer volume 14, Article number: 177 (2015)
Apoptosis-stimulating of p53 protein 2 (ASPP2) is one of the ASPP family members and it has been reported to be associated with human cancer. However, the role of it in pancreatic cancer is still not clear.
We analyzed the expression level of ASPP2 in cancer tissue samples with RT-qPCR, Western Blotting assay and immunohistochemistry staining. We studied the biological function of ASPP2 and its mechanism with gene overexpression and gene silencing technologies. We determined the sensitivity of pancreatic cells with differential ASPP2 level to gemcitabine and whether autophagy inhibition affected the gemcitabine resistance, both in vitro and in vivo.
Expression of ASPP2 was downregulated in cancerous tissues in comparison with para-cancerous tissues. ASPP2 expression was linked to clinical outcomes in patients and down-regulation of ASPP2 increased cell proliferation, autophagic flux, the activity of AMP Kinase of pancreatic cancer cells and vice versa. Knockdown of ASPP2 results in increased resistance to gemcitabine, which was attributed to the enhanced autophagy.
ASSP2 expression is lower in cancerous tissues and decreased ASPP2 lead to higher cancer cells proliferation and autophagic flux, which contribute to the gemcitabine resistance.
Pancreatic cancer (PC) is the fourth leading cause of cancer-related deaths in the world with 5-year survival rate of 4 %.[1, 2] Currently, the main therapeutic options include surgical resection, radiation therapy, chemotherapy and immunotherapy. However, in most cases after surgery treatment, the tumor recurs within 1–2 years and patients develop metastasis.  In case of patients with inoperable PC, the standard treatment is chemotherapy. In this group, the survival of the patients is just increased by a dismal 5 weeks.[3, 4] The poor outcome of chemotherapy is partly due to the drug-resistant phenotype of PC cells.[5–9] however, the mechanism is not fully elucidated. Thus, failure of effective chemotherapy results in high mortality in PC patients, which the importance of understanding the mechanism of drug resistance and developing strategies that would improve the outcome of chemotherapy.
ASPP2 is a pro-apoptotic regulator that belongs to ASPP family. The expression of ASPP2 is frequently suppressed in many cancers in relation to enhanced apoptosis through the binding to p53 for transcriptional transactivation.[11–15] Surprisingly, a number of ASPP2 binding partners that are involved in biological pathways other than apoptosis have also been identified, suggesting that ASPP2 function is far more complex than simply enhancing p53-mediated apoptosis.
Autophagy acts as a survival mechanism under conditions of stress, maintaining cellular integrity by regenerating metabolic precursors and clearing subcellular debris . Autophagy is wildly involved in the tumorous development and drug resistance.[17–20] A recent study has found that ASPP2 inhibits RAS-induced autophagy by preventing ATG16/ATG5/ATG12 formation and induces autophagic apoptosis by releasing Beclin-1 from cytoplasmic Bcl-2-Beclin-1 complexes in hepatoma cells.[21, 22] However, the function and detailed mechanism of ASPP2 which regulate autophagy is still not clear, especially in pancreatic cancer. In this study, we investigated the role and mechanism of ASPP2 for pancreatic cancer drug resistance.
Our data suggest that ASPP2 express lower in pancreatic cancer cells in comparison with para-cancer cells and decrease of ASPP2 expression is also linked to poor clinical outcomes in patients. Additionally, the decreased expression of ASPP2 can lead to enhanced autophagy through AMP kinase pathway in pancreatic cancer and resistance to gemcitabine in vitro and in vivo. Furthermore, the anticancer activity of ASPP2 in pancreatic cancer is partially due to its regulation on autophagy. Our study highlights ASPP2 and autophagy can be targeted for improvement of the efficiency of gemcitabine treatment and development of novel anti-pancreatic cancer drugs.
ASSP2 expression is lower in cancerous tissues and predicts a poor prognosis
ASPP2 plays a key role in apoptosis regulation in the intrinsic and extrinsic apoptotic pathways [23, 24] and widely expressed in many human tissues. The expression of ASPP2 can be enhanced in response to DNA damage, and was down-regulated in both metastatic and invasive cells as compared to normal breast epithelium. To exam the levels of expression of ASSP2 in the pancreatic cancer tissues and para-cancerous tissues, we determined ASSP2 expression level with RT-qPCR assay or immunoblotting assay, the ASSP2 expression level was less abundant in pancreatic cancer tissues compared with para-cancerous tissues (Fig. 1a and b). We also analyzed the patients’ samples with IHC assay (Table 1). As presented in Fig. 1c (left panel, 1# and 11# samples as the representative samples), the results suggest that ASSP2 protein expression was much lower in cancerous tissues (Fig. 1c, right panel). Furthermore, the ASPP2 low expression patients were found to exhibit high Histopathological grade (Table 1). More importantly, significant differences in both overall survival and disease-free survival were found among ASPP2 low/high groups (Fig. 1d). Taken together, all the data suggest that ASSP2 expression is lower in cancerous tissues than papa-cancerous tissues and it could be an independent prognostic predictor for pancreatic cancer.
ASPP2 inhibit proliferation of pancreatic cancer cell
To study the role of ASSP2 in cancer, we firstly analyzed its expression in series of pancreatic cancer cell lines using NCBI GEO database  and the data suggest that ASSP2 expression significantly differs in different PC cell lines. Low ASPP2 expression cell line BxPC-3 and high ASPP2 expression cell line SW1990 were used for further research (Fig. 2a). We organized ASPP2 stably over-expression cell lines in BxPC-3 and ASPP2 stably knockdown cell lines in SW1990, the mRNA and protein expression of ASPP2 were shown (Fig. 2b, c and Additional file 1: Figure S1A). The #2 of ASPP2 knockdown cell lines was used for next experiments. Forced ASPP2 over-expression resulted in a significant decrease of cancer cell proliferation, Knockdown of ASPP2 enhanced proliferative activity (Fig. 2d). Consistently, over-expression of ASPP2 attenuated cancer cell clone formation and vice versa (Fig. 2e). Together, these results reveal that down-regulation of ASPP2 could enhance cell proliferation of pancreatic cancer.
ASPP2 negatively regulate basal autophagy in pancreatic cancer cell lines
Recently, two groups found that ASPP2 could regulate survival autophagy and autophagic apoptosis through different ways in hepatoma cells,[21, 22] which indicated that ASPP2 could be the Indispensable regulator in autophagy. In pancreatic cancer, autophagy play essential function in cell growth under basal condition. To examine its regulation on basal autophagy, firstly, we analyzed the autophagic activities of pancreatic cancer cell lines. Unexpectedly, BxPC-3 cells with low ASPP2 expression expressed higher LC3-II, the marker of autophagosomes, sw1990 cells with high ASPP2 expression formatted less LC3-II (Fig. 3a). For directly observing the autopahgy process, we also transfected GFP-LC3 into these four PC cell lines and analyze the formation of autophagosomes, we found that more autophagosomes were formed in the BxPC-3 cells than SW1990, PANC1and MiAPaca-2 cells (Fig. 3b). All the data presented suggest that autophagy negatively correlated with the expression of ASPP2.
Based on these data, we hypothesized that ASSP2 can negatively regulate basal autophagy in pancreatic cancer cells. To test this hypothesis, we checked the Autophagy-Related Gene Family in BxPC-3 cells with ASPP2 overexpression and in SW1990 cells with ASPP2 knockdown. Overexpression of ASPP2 could significantly decrease the amount of LC3-II and ATG family expression, and knockdown of ASPP2 enhanced it (Fig. 3c). With GFP-LC3 system, we confirmed the regulation of ASPP2 in autophagy (Fig. 3d). In addition, as presented in Fig. 3e, the accumulation of autophagic vacuoles was dramatically decreased in ASPP2 overexpression BxPC3 cells and silencing of ASPP2 reversed it. Furthermore, for detecting the autophagic flux, we examined mRFP-GFP-LC3 puncta formation with fluorescence microscope. Consistently, ASPP2 decreased the autophagosomal-lysosomal fusion process, which also supports ASPP2 as the negative regulator for autophagy under basal condition (Fig. 3f). As a P53 interacting-protein,ASPP2 often regulate cell function in P53-dependent way. P53 was also reported as the core-regulator in autophagy. to exclude the function of P53 in the regulation of autophagy, we also check the basal autophagy with P53 inhibitor, pifithrin-α . However, inhibition of P53 could not reverse the function of ASPP2 in autophagy, which suggested that ASPP2 regulated basal autophagy in P53-indepdent way (Additional file 1: Figure S1B).
ASPP2 regulate autophagy through AMPK-mTOR pathways
AMPK is a key cellular energy sensor and functions to maintain energy homeostasis upon nutrient starvation, it could regulate autophagy through mTOR pathway. Firstly, we checked the phosphorylation of AMPK and TSC2. Down-regulation of ASPP2 could increase the phosphorylation of AMPK and TSC2 and vice versa (Fig. 4a). For confirming the ASPP2 regulate autophagy through AMPK, we knockdown the AMPK expression with shRNA (Fig. 4b),and found that AMPK knockdown could significantly inhibit the autophagic flux upregulation induced by ASPP2 knockdown (Fig. 4c,d,e). These results indicate that ASPP2 regulate autophagy through AMPK-mTOR pathways.
ASPP2 can facilitate gemcitabine induced cell apoptosis through regulation of autophagy in vitro and in vivo
Gemcitabine is currently the standard chemotherapy treatment at all stages of pancreatic cancer. Survival benefit and clinical impact however remain moderate due to a high degree of drug resistance. To dissect the effect of ASPP2 on gemcitabine mediated cell apoptosis, we treated these cells with gemcitabine. As shown in Fig. 5a, overexpression of ASPP2 can promote the gemcitabine induced cell death and knockdown of ASPP2 could inhibit it. To further define the role of ASPP2 in determining the sensitivity of PC to gemcitabine, we checked the cell apoptosis induced by gemcitabine, which is consistently with the cell death results (Fig. 5b). Apoptosis protein expression also proved it (Fig. 5c). All the results suggest that ASPP2 expression level can determine the susceptibility of the cells to gemcitabine treatment.
As ASPP2 could interact with P53 to Specifically Stimulate the Apoptotic Function of p53, we firstly checked that whether ASPP2 regulated gemcitabine-resistance in pancreatic cancer. With pifithrin-α treatment, we found that inhibition of P53 could not reverse the ASPP2-inudced cell apoptosis, which suggested that ASPP2 regulated gemcitabine-induced cell death in P53-indepdent way (Fig. 5d,e). As shown previously, ASPP2 can negatively regulate autophagic activity, so we next exam whether ASPP2 determining the susceptibility of cells to gemcitabine is dependent on its regulation of autophagy. To answer this question, we treated ASPP2 shRNA transduced SW1990 cells with gemcitabine in the presence or absence of CQ and 3-MA, which are the widely used autophagy inhibitors, and cell death and cell apoptosis were analyzed. The protection of knockdown of ASPP2 in SW1990 cells from gemcitabine induced apoptosis was dramatically impaired in the presence of autophagy inhibitors, suggesting that ASPP2 regulate gemcitabine induced cell apoptosis via autophagy (Fig. 6a, b, c). To dissect the ASPP2 role in regulation of gemcitabine induced cell apoptosis in vivo, we inoculated SW1990 cells with ASPP2 knockdown into nude mice and determine the tumor size at indicated time point post-inoculation. As shown in Fig. 6d and e, ASPP2 knockdown cells were more resistant to gemcitabine treatment; however, this is significantly impaired following treatment of CQ, further establishing the essential role of autophagy in determining the resistance to gemcitabine in vivo. Collectively, all the data presented here demonstrate that decrease expression of ASPP2 can confer cell the insensitivity to gemcitabine, which is dependent on its activation of autophagy.
The capability of cancer cells to escape the cytotoxic effect of chemotherapeutic drug may result from genetic mutations that affect cell cycle, apoptosis or accumulation of drugs inside of the cell.[35, 36] In this study, we revealed the mechanisms by which pancreatic cancer cells to escape chemotherapeutic drug (gemcitabine) mediated cell apoptosis via decrease of ASPP2 expression to activate the autophagic activity.
We found that ASPP2 expression level was preferentially down-regulated in cancerous tissues compared with para-cancerous tissues from the pancreatic cancer patients. ASPP2 expression levels were different in distinct PC cell lines and ASPP2 could negatively regulated cancer cell proliferation. We found that the expression levels of ASPP2 negatively associated with the autophagic activities in the pancreatic cancer cell lines. Through overexpression and knockdown of ASPP2, we demonstrated that ASPP2 can negatively regulate autophagic activity. Furthermore, we demonstrated that ASPP2 regulated autophagy through AMPK-mTOR pathways. We also found that ASPP2 could promote the gemcitabine induced cell apoptosis in pancreatic cancer cells, and knockdown ASPP2 can enable the phenotype of the cells to resistant for gemcitabine treatment. In addition, the effect of protecting cells from gemcitabine treatment through knockdown of ASPP2 was significantly compromised by repression of autophagy in vitro and in vivo, indicating that ASPP2 determining the sensitivity of pancreatic cancer cells to gemcitabine was dependent on its regulation of autophagy (Fig. 6f).
Autophagy is the ubiquitous cellular process that involves cell degradation of unnecessary or dysfunctional cellular components through the lysosomal machinery; it plays a critical role in removing protein aggregates, as well as damaged or excess organelles, to maintain intracellular homeostasis . Autophagy is widely involved in many physiological process, such as cell survival, embryo development, longevity, clearance of toxic aggregate-prone proteins, cell surface receptor trafficking and protection of host from pathogen infection.[19, 38–40] Dysregulation of autophagy contributes to a number of diseases including tumorigenesis.[17, 19] However, the role of autophagy in cancer is still controversial. It was reported that inhibition of autophagy can increase chemotherapy-induced apoptosis in hepatocarcinoma cells, colon cancer, and esophageal cancer cells. In our study, we found that the decrease of ASPP2 could enhance the autophagic activity of pancreatic cancer cells, and this lead to pancreatic cancer cells less sensitive to gemcitabine induced cell apoptosis in vitro and in vivo; Lower expression of ASPP2 was also correlated with poor outcome of gemcitabine treatment and survival rates. We also found that ASPP2 was down-regulated in the pancreatic cancer tissues compared with para-pancreatic cancer tissues, suggesting that decrease of ASPP2 leading to upregulated autophagy might serve as a chemotherapy intrinsic defense mechanism for pancreatic cancer cells.
Taken together, the data provide new insights into the mechanisms by which decrease of ASPP2 in pancreatic cancer cells can interfere with the effectiveness of chemotherapy via enhanced autophagy. These results reveal ASPP2 as a crucial and unexpected switch for the sensitivity to gemcitabine phenotype of pancreatic cancer via regulation of autophagy, which suggests that in ASPP2 low expression patients gemcitabine combined autophagy inhibitors could significantly promote cancer cell apoptosis. Our data identify a molecular link between aberrant ASPP2 expression in pancreatic cancer and susceptibility to gemcitabine treatment. A better understanding of this process may lead us to new methods to overcome drug resistance in this aggressive disease.
Patients and samples
Twelve cancer tissues were (for qRT-PCR and WB) from the patients which receiving curative resection in Changhai Hospital, Shanghai, China from January 2013 to January 2014. 65 pancreatic cancer tissues (for IHC) were randomly retrieved from pancreatic cancer patients receiving curative resection in Changhai Hospital, Shanghai, China from January 2008 to January 2010 (see detailed clinical pathologic features in Table 1). All patients were followed up until January 2013, with a median observation time of 21 months. Matched pairs of primary pancreatic cancer samples and adjacent pancreatic tissues were used for analysis of ASPP2 expression. Participants provide their written informed consent to participate in this study, and this study was performed in according to an established protocol approved by the Ethic Committee of Changhai Hospital.
Cell culture and reagent
Human pancreatic cancer cell lines BxPc-3, SW1990, Panc-1 and MiaPaCa-2 were purchased from Cell Bank of Type Culture Collection of Chinese Academy of Sciences. They were cultured in 10 % FBS DMEM/RPMI1640 at 37 °C and 5 % CO2. Autophagy inhibitors, 3-MA and chloroquine were purchased from Sigma (San Diego, CA). ASPP2 antibody (sc-53861) is mouse monoclonal IgG1 against amino acids 691–1128 of ASPP2 of human origin. The following antibodies were used for Western blot: AMPK, p-AMPK, Actin (Santa Cruz), p-TSC2, TSC2, Atg5, Atg7, Beclin1, p62, LC3 (Cell signal technology).
Total RNA was extracted by using Trizol reagent (Invitrogen, Carlsbad, CA), and the reverse-transcription reactions were performed using an M-MLV Reverse Transcriptase kit (Invitrogen). Real-time PCR was performed using a standard SYBR Green PCR kit (Toyobo, Osaka, Japan). The primers used in RT-PCR as Followed. mRNA levels are calculated as fold change of control.
Sequence of primers for real-time PCR
|Primer||Sequence (5′ to 3’)|
|ASPP2 forward primer||5’-TAAGCAATGGGAAACTTGTGG-3’|
|ASPP2 reverse primer||5’-CATCCGAGGCATAGTAGACGA-3’|
|18 s forward primer||5’-CGGCTACCACATCCAAGGAA-3’|
|18 s reverse primer||5’-GCTGGAATTACCGCGGCT-3’|
We generated plasmid vectors encoding shRNAs targeting ASPP2/AMPK or scramble shRNA using pENTR™/U6 expression vector (Invitrogen, Carlsbad, CA), and designated them as sh-Con and sh-ASPP2/sh-AMPK, respectively. The synthesized oligonucleotides were as follows:
|ASPP2#1||5’-CACCGCAGAATGCCAAGCTACAACACGAATGTTGTAGCTTGGCATTCTGC -3’||5’-AAAAGCAGAATGCCAAGCTACAACATTCGTGTTGTAGCTTGGCATTCTGC -3’|
|ASPP2#2||5’-CACCGCTGCAGTAGGTCCCTATATCCGAAGATATAGGGACCTACTGCAGC -3’||5’-AAAAGCTGCAGTAGGTCCCTATATCTTCGGATATAGGGACCTACTGCAGC -3’|
|ASPP2#3||5’-CACCGCGTCCGTTCTCAATGTTTGACGAATCAAACATTGAGAACGGACGC -3’||5’-AAAAGCGTCCGTTCTCAATGTTTGATTCGTCAAACATTGAGAACGGACGC -3’|
|AMPK#1||5’-CACCGCTTGATGCACACATGAATGCCGAAGCATTCATGTGTGCATCAAGC -3’||5’-AAAAGCTTGATGCACACATGAATGCTTCGGCATTCATGTGTGCATCAAGC -3’|
|AMPK#2||5’-CACCGCAGGCCCAGAGGTAGATATACGAATATATCTACCTCTGGGCCTGC -3’||5’-AAAAGCAGGCCCAGAGGTAGATATATTCGTATATCTACCTCTGGGCCTGC -3’|
|AMPK#3||5’-CACCGCAGAAGTATGTAGAGCAATCCGAAGATTGCTCTACATACTTCTGC -3’||5’-AAAAGCAGAAGTATGTAGAGCAATCTTCGGATTGCTCTACATACTTCTGC -3’|
The cancer cells were seeded in 100 μl growth medium including 5 × 103 cells per well in 96-well plates. Cells were treated with indicated regents or not. Every 24 h until 72 h, CCK-8 solution was added to wells and incubation at 37 °C for 2 h. Cell viability was measured. Viability is given as a percent of the control value.
Colony formation assay
Five hundred cancer cells per well were seeds in 6-wells plate. After cultured for 2–3 weeks, we terminate cell culture and wash the plate with PBS for two times, fixed cells with 4 % Paraformaldehyde for 15 min, Incubate cells with trypan blue for 10 min and wash the staining solution.
The Annexin V-FITC Apoptosis Detection Kit was purchased from eBioscience, Inc. (San Diego, CA) and used as recommended by manufacturer’s instruction.
Western blot analysis was carried out on 10 % SDS–PAGE. Briefly, proteins were electrotransferred onto nitrocellulose filter. After blocking for 1 h in PBS with 0.1 % Tween 20 (PBST) and 5 % BSA, the membranes were incubated over night with specified primary antibody in PBST containing 5 % BSA. Detection was carried out by the use of HRP conjugated IgG assay kit (Sigma, St. Louis, MO). The former band was stripped with Stripping buffer (P0025, Beyotime) and incubated with other antibodies. the relative density of WB bands with ImageJ2X.
Transmission electron microscopy
Cells were fixed for 1 h at 4 °C in 1.6 % glutaraldehyde in 0.1 M Sörensen phosphate buffer (pH 7.3), washed, fixed again in aqueous 2 % osmium tetroxide and finally embedded in Epon. Electron microscopy was performed with a JEM-2000 EX transmission electron microscope, on ultrathin sections (45 nm) stained with lead citrate and uranyl acetate.
Immunohistochemistry was performed using EnVisiontm system in according to the manufacture’s instruction. The antibody against ASPP2 (Santa Cruz) was tested on sections from formalin-fixed paraffin-embedded pancreatic cancer and para-cancerous tissue samples. Images were obtained with a Zeiss AXIO Imager. A1 microscope (Zeiss, Jena, Germany) equipped with an AxioCam (Zeiss) and the AxioVision 4.6 software (Zeiss). The density of ASPP2 positive staining was measured by a computerized image system (Leica Microsystems Imaging Solutions Ltd, Cambridge, United Kingdom). The patients were divided to two groups (“low ASPP” and “high ASPP”) according to median of ASPP2 expression in cancer samples.
Tumor xenograft study
All animal experimentation proceeds according to the Standard of IACUC (Institutional Animal Care and Use Committee) and performs in according to an established protocol approved by the Ethic Committee of Changhai Hospital. 2 × 106 cells Cancer cells were introduced by subcutaneous implantation of in 10 % FBS DMEM into 6-week-old immunodeficient nude mice. 1 week later, Gemcitabine (40 mg/kg) with or without Chloroquine (CQ, 45 mg/kg) was injected every 2 days into tumors. The mice were sacrificed 5 weeks after tumor implantation. The volumes of tumors were measured and calculated as V = a x b2 x π/6.
Apoptosis-stimulating of p53 protein 2
Reverse Transcription Quantitative Polymerase Chain Reaction
Short hairpin RNA
Adenosine 5’-monophosphate (AMP)-activated protein kinase
Green Fluorescent Protein
Red fluorescent protein
Hidalgo M. Pancreatic cancer. N Engl J Med. 2010;362:1605–17.
Maitra A, Hruban RH. Pancreatic cancer. Annu Rev Pathol. 2008;3:157–88.
Strimpakos A, Saif MW, Syrigos KN. Pancreatic cancer: from molecular pathogenesis to targeted therapy. Cancer Metastasis Rev. 2008;27:495–522.
Vincent A, Herman J, Schulick R, Hruban RH, Goggins M. Pancreatic cancer. Lancet. 2011;378:607–20.
Zheng C, Jiao X, Jiang Y, Sun S. ERK1/2 activity contributes to gemcitabine resistance in pancreatic cancer cells. J Int Med Res. 2013;41:300–6.
Iwagami Y, Eguchi H, Nagano H, Akita H, Hama N, Wada H, et al. miR-320c regulates gemcitabine-resistance in pancreatic cancer via SMARCC1. Br J Cancer. 2013;109:502–11.
Horiguchi S, Shiraha H, Nagahara T, Kataoka J, Iwamuro M, Matsubara M, et al. Loss of runt-related transcription factor 3 induces gemcitabine resistance in pancreatic cancer. Mol Oncol. 2013.
Chen YW, Liu JY, Lin ST, Li JM, Huang SH, Chen JY, et al. Proteomic analysis of gemcitabine-induced drug resistance in pancreatic cancer cells. Mol Biosyst. 2011;7:3065–74.
Yokoi K, Fidler IJ. Hypoxia increases resistance of human pancreatic cancer cells to apoptosis induced by gemcitabine. Clin Cancer Res. 2004;10:2299–306.
Sullivan A, Lu X. ASPP: a new family of oncogenes and tumour suppressor genes. Br J Cancer. 2007;96:196–200.
Liu ZJ, Zhang Y, Zhang XB, Yang X. Abnormal mRNA expression of ASPP members in leukemia cell lines. Leukemia. 2004;18:880.
Mori T, Okamoto H, Takahashi N, Ueda R, Okamoto T. Aberrant overexpression of 53BP2 mRNA in lung cancer cell lines. FEBS Lett. 2000;465:124–8.
Bergamaschi D, Samuels Y, Jin B, Duraisingham S, Crook T, Lu X. ASPP1 and ASPP2: common activators of p53 family members. Mol Cell Biol. 2004;24:1341–50.
Lossos IS, Natkunam Y, Levy R, Lopez CD. Apoptosis stimulating protein of p53 (ASPP2) expression differs in diffuse large B-cell and follicular center lymphoma: correlation with clinical outcome. Leuk Lymphoma. 2002;43:2309–17.
Vives V, Su J, Zhong S, Ratnayaka I, Slee E, Goldin R, et al. ASPP2 is a haploinsufficient tumor suppressor that cooperates with p53 to suppress tumor growth. Genes Dev. 2006;20:1262–7.
Choi AM, Ryter SW, Levine B. Autophagy in human health and disease. N Engl J Med. 2013;368:651–62.
Liang XH, Jackson S, Seaman M, Brown K, Kempkes B, Hibshoosh H, et al. Induction of autophagy and inhibition of tumorigenesis by beclin 1. Nature. 1999;402:672–6.
Kimmelman AC. The dynamic nature of autophagy in cancer. Genes Dev. 2011;25:1999–2010.
Levine B. Unraveling the role of autophagy in cancer. Autophagy. 2006;2:65–6.
Kondo Y, Kanzawa T, Sawaya R, Kondo S. The role of autophagy in cancer development and response to therapy. Nat Rev Cancer. 2005;5:726–34.
Liu K, Shi Y, Guo X, Wang S, Ouyang Y, Hao M, et al. CHOP mediates ASPP2-induced autophagic apoptosis in hepatoma cells by releasing Beclin-1 from Bcl-2 and inducing nuclear translocation of Bcl-2. Cell Death Dis. 2014;5, e1323.
Wang Y, Wang XD, Lapi E, Sullivan A, Jia W, He YW, et al. Autophagic activity dictates the cellular response to oncogenic RAS. Proc Natl Acad Sci U S A. 2012;109:13325–30.
Kobayashi S, Kajino S, Takahashi N, Kanazawa S, Imai K, Hibi Y, et al. 53BP2 induces apoptosis through the mitochondrial death pathway. Genes Cells. 2005;10:253–60.
Samuels-Lev Y, O’Connor DJ, Bergamaschi D, Trigiante G, Hsieh JK, Zhong S, et al. ASPP proteins specifically stimulate the apoptotic function of p53. Mol Cell. 2001;8:781–94.
Trigiante G, Lu X. ASPP [corrected] and cancer. Nat Rev Cancer. 2006;6:217–26.
Sgroi DC, Teng S, Robinson G, LeVangie R, Hudson Jr JR, Elkahloun AG. In vivo gene expression profile analysis of human breast cancer progression. Cancer Res. 1999;59:5656–61.
Barrett T, Troup DB, Wilhite SE, Ledoux P, Rudnev D, Evangelista C, et al. NCBI GEO: mining tens of millions of expression profiles--database and tools update. Nucleic Acids Res. 2007;35:D760–5.
Yang S, Wang X, Contino G, Liesa M, Sahin E, Ying H, et al. Pancreatic cancers require autophagy for tumor growth. Genes Dev. 2011;25:717–29.
Kabeya Y, Mizushima N, Ueno T, Yamamoto A, Kirisako T, Noda T, et al. LC3, a mammalian homologue of yeast Apg8p, is localized in autophagosome membranes after processing. EMBO J. 2000;19:5720–8.
Tasdemir E, Maiuri MC, Galluzzi L, Vitale I, Djavaheri-Mergny M, D’Amelio M, et al. Regulation of autophagy by cytoplasmic p53. Nat Cell Biol. 2008;10:676–87.
Tang YL, Huang LB, Tian Y, Wang LN, Zhang XL, Ke ZY, et al. Flavokawain B inhibits the growth of acute lymphoblastic leukemia cells via p53 and caspase-dependent mechanisms. Leuk Lymphoma. 2015;1–10.
Kahn BB, Alquier T, Carling D, Hardie DG. AMP-activated protein kinase: ancient energy gauge provides clues to modern understanding of metabolism. Cell Metab. 2005;1:15–25.
Shaw RJ, Bardeesy N, Manning BD, Lopez L, Kosmatka M, DePinho RA, et al. The LKB1 tumor suppressor negatively regulates mTOR signaling. Cancer Cell. 2004;6:91–9.
O’Reilly EM. Pancreatic adenocarcinoma: new strategies for success. Gastrointest Cancer Res. 2009;3:S11–5.
Lu Z, Kleeff J, Shrikhande S, Zimmermann T, Korc M, Friess H, et al. Expression of the multidrug-resistance 1 (MDR1) gene and prognosis in human pancreatic cancer. Pancreas. 2000;21:240–7.
Krishna R, Mayer LD. Multidrug resistance (MDR) in cancer. Mechanisms, reversal using modulators of MDR and the role of MDR modulators in influencing the pharmacokinetics of anticancer drugs. Eur J Pharm Sci. 2000;11:265–83.
Kroemer G, Marino G, Levine B. Autophagy and the integrated stress response. Mol Cell. 2010;40:280–93.
Levine B, Mizushima N, Virgin HW. Autophagy in immunity and inflammation. Nature. 2011;469:323–35.
Mizushima N, Levine B. Autophagy in mammalian development and differentiation. Nat Cell Biol. 2010;12:823–30.
Singh R, Kaushik S, Wang Y, Xiang Y, Novak I, Komatsu M, et al. Autophagy regulates lipid metabolism. Nature. 2009;458:1131–5.
Guo XL, Li D, Hu F, Song JR, Zhang SS, Deng WJ, et al. Targeting autophagy potentiates chemotherapy-induced apoptosis and proliferation inhibition in hepatocarcinoma cells. Cancer Lett. 2012;320:171–9.
Li J, Hou N, Faried A, Tsutsumi S, Kuwano H. Inhibition of autophagy augments 5-fluorouracil chemotherapy in human colon cancer in vitro and in vivo model. Eur J Cancer. 2010;46:1900–9.
O’Donovan TR, O’Sullivan GC, McKenna SL. Induction of autophagy by drug-resistant esophageal cancer cells promotes their survival and recovery following treatment with chemotherapeutics. Autophagy. 2011;7:509–24.
We would like to express our appreciation to Dr. Wen Wen for their constructive supervision and discussion.
The authors declare no conflict of financial competing interests and non-financial competing interests.
BS, QB and YJZ carried out the molecular genetic studies and drafted the manuscript. CHS and GL participated in the sequence alignment. AAL carried out the immunoassays. WJ and RL participated in the design of the study. YQZ performed the statistical analysis. GJ and XGH conceived of the study, and participated in its design and coordination and helped to draft the manuscript. All authors read and approved the final manuscript.
Bin Song, Qi Bian and Yi-Jie Zhang contributed equally to this work.
(A) The expression of ASPP2 was detected in BxPC-3 cells with stable ASSP2 over-expression and SW1990 cells with ASPP2 knockdown. (B) Indicated molecules were measured with immunoblots in BxPC-3 cells with stable ASSP2 over-expression treated with pifithrin-α (10 μM). (JPEG 139 kb)
About this article
Cite this article
Song, B., Bian, Q., Zhang, Y. et al. Downregulation of ASPP2 in pancreatic cancer cells contributes to increased resistance to gemcitabine through autophagy activation. Mol Cancer 14, 177 (2015). https://doi.org/10.1186/s12943-015-0447-5
- Pancreatic cancer
- Drug resistance