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Introduction

Prostate cancer is a common type of cancer in men and the second leading cause of malignant tumor-related mortality. In the United States, an estimated 26,120 deaths were attributed to prostate cancer in 2016 (1). Androgen deprivation therapy (ADT) has been shown to be an effective treatment for prostate cancer, proving indispensable for advanced-stage prostate cancer (2–4). However, the majority of prostate cancer cases develop into castration-resistant prostate cancer (CRPC) following ADT within 2 years (5,6), despite the circulating testosterone levels being decreased to ‘castrate level’. CRPC is associated with poor survival rates, and currently, no effective methods exist to prevent progression (7). Therefore, determining the molecular mechanism that promotes CRPC and identifying novel targets for CRPC treatment are important.

Serine/threonine protein phosphatase 2A (PP2A) is a tumor-suppressive factor that has been discovered to participate in numerous signaling pathways, including PI3K/Akt/mTOR, Wnt/β-catenin and c-Myc pathways (8). It was previously reported that the deregulation of PP2A and its regulatory subunits was commonly observed in breast cancer, and such an event was associated with an unfavorable outcome (9). The subsequent restoration of PP2A, due to its functional deficiency in colorectal cancer, was also revealed to enhance the patient response to chemotherapy (10). The expression levels of PP2A have been found to be downregulated in various types of cancer, such as breast (9), colorectal (10) and lung cancer (11), as well as acute myeloid leukemia (12); however, to the best of our knowledge, few studies have reported the changes in the expression levels during prostate cancer tumorigenesis and its effect on apoptosis and chemoresistance. Therefore, determining the effect of PP2A on the development of prostate cancer is of great significance.

X-linked inhibitor of apoptosis (XIAP) is an antiapoptotic factor whose expression has been found to be upregulated in various types of cancer, such as bladder cancer (13), renal cell carcinoma (14) and acute myeloid leukemia (15). The upregulated expression of XIAP was reported in ovarian carcinoma and esophageal carcinoma cell lines, which were found to be insensitive to chemotherapy (16,17). A previous study also demonstrated that the expression levels of XIAP were markedly upregulated in CRPC tissues and cells compared with those in androgen-sensitive tissues and cells (18). PP2A participates in the cell cycle and apoptosis (19). Previous research revealed that dephosphorylation of eukaryotic initiation factor 4B (eIF4B) at serine 406 was mediated by PP2A (20). In addition, another study revealed that pim-2 proto-oncogene serine/threonine kinase (Pim-2) was upregulated in prostate cancer, and suggested that the Pim-2/eIF4B/XIAP signaling pathway may participate in the progression of prostate cancer (21). Furthermore, Pim-2 was discovered to directly phosphorylate eIF4B on serine 406 (22), which indicated that XIAP may be a downstream factor of eIF4B. Thus, determining the downstream factor of eIF4B within the PP2A signaling pathway and the antiapoptotic effect of PP2A are of critical importance. The present study investigated whether restoration of PP2A promotes apoptosis and facilitates docetaxel sensitivity via the PP2A/p-eIF4B/XIAP signaling pathway in prostate cancer.

Materials and methods

Cell culture and treatment

The human prostate cancer cell line, LNCaP, was purchased from Shanghai Biowing Applied Biotechnology Co. Ltd. The DU145 and PC-3 cell lines were purchased from Shanghai Zhong Qiao Xin Zhou Biotechnology Co., Ltd. The LNCaP cell line was cultured in RPMI-1640 medium (Corning, Inc.) and supplemented with 10% FBS (Gibco; Thermo Fisher Scientific, Inc.). The DU145 and PC-3 cell lines were cultured in Eagle's Minimum Essential Medium (cat. no. ZQ-301; Shanghai Zhong Qiao Xin Zhou Biotechnology Co., Ltd.), supplemented with Earle's salts, L-glutamine, non-essential amino acids, NaHCO3, 10% FBS and 1% penicillin-streptomycin. All the cell lines were maintained at 37°C in a humidified incubator with 5% CO2. Trypsin was used for cell dissociation (HyClone; Cytiva).

To increase the expression level of PP2A, an agonist of PP2A, DT061 (10 µmol/l; cat. no. 112929; MedChemExpress), was used to treat the DU145 and PC-3 cell lines. DT061 was dissolved in DMSO (10 µmol/l). The control group contained cells treated with DMSO only. All the cell lines were maintained at 37°C in a humidified incubator with 5% CO2 for 48 h. The cell lines were also treated with increasing concentrations of docetaxel (0.00, 0.05, 0.50, 1.00, 2.00, 5.00, 50.00, 200.00 and 500.00 nM; cat. no. HY-B0011; MedChemExpress) at 37°C for 48 h.

Cell transfection

Cell transfection was performed at 37°C for 6 h using Lipofectamine® 2000 (Invitrogen; Thermo Fisher Scientific, Inc.). Subsequent experimentation was performed 48 h after transfection, according to the manufacturer's protocol. Briefly, the LNCaP cell line was seeded into six-well plates, at a density of 1.2×105 cells/well, and upon reaching 65–70% confluence, the medium was changed to 2 ml RPMI-1640 medium (Gibco; Thermo Fisher Scientific, Inc.), supplemented with 5 µl Lipofectamine 2000 reagent and 5 µl (20 µM) small interfering (si)RNA. The siRNAs used, which were purchased from Shanghai GenePharma Co., Ltd. (cat. no. A10001), were as follows: siPP2A-1 (siRNA1), 5′-CACCGAAUUUAUGGGAAAUTT-3′; siPP2A-2 (siRNA2), 5′-GGGCAUUGUACUUCUGGAATT-3′; siPP2A-3 (siRNA3), 5′-GACCUUACUAGCUCAUACATT-3′; and si-negative control (NC), 5′-UUCUCCGAACGUGUCACGUTT3′. The siRNA used in the cell transfection was siPP2A-2 (siRNA2). The NC siRNA used was a scramble non-targeting sequence.

Cell Counting Kit (CCK)-8 assay

Cell viability was analyzed using a CCK-8 assay (Dojindo Molecular Technologies, Inc.). Briefly, the DU145 and PC-3 cell lines were treated with 10 µM DT061 (dissolved in DMSO) at 37°C for 48 h, then seeded into 96-well flatbottomed microplates, at a density of 5×103 cells/well. Increasing concentrations (0, 0.05, 0.5, 1, 2, 5, 50, 200 and 500 nM) of docetaxel were subsequently added to each well and the cells were incubated at 37°C for 48 h; each well contained a volume of 100 µl, consisting of 90 µl cell suspension and 10 µl docetaxel solution. Following incubation for 48 h at 37°C, CCK-8 reagent was added to each well at 37°C for 1 h and the absorbance was measured at 450 nm.

For the LNCaP cell line, the cells were first transfected with siRNA at 37°C for 48 h, then seeded into 96-well flatbottomed microplates, at a density of 5×103 cells/well. Next, docetaxel was added to each well at gradient concentrations (0, 0.05, 0.5, 1, 2, 5, 50, 200 and 500 nM). Following incubation at 37°C for 48 h, CCK-8 reagent was added to each well and the cells were incubated at 37°C for 1 h, and the absorbance was measured at 450 nm.

Reverse transcription-quantitative PCR (RT-qPCR)

Total RNA was extracted from the DU145, PC-3 and LNCaP cell lines. using TRIzol® (Takara Biotechnology Co., Ltd.). SYBR Green was used as the fluorophore (MedChemExpress). Total RNA was reverse transcribed into cDNA using random primers and a RT Master Mix for qPCR (gDNA digester plus), according to the manufacture's protocol (cat. no. HY-K0511; MedChemExpress). The following thermocycling conditions were used for RT: 25°C for 5 mins, 42°C for 40 mins and 85°C for 2 mins. The following thermocycling conditions were used for qPCR: Initial denaturation at 94°C for 2 min, followed by 35 cycles at 94°C for 40 sec, 50°C for 40 sec and 72°C for 1 min and final extension at 72°C for 5 min. PP2A expression was subsequently determined using qPCR and the following primers: Human PP2A forward, 5′-AGAAGAGGATGAACCCACGC-3′ and reverse, 5′-TGCTAGGCTGGAAATCAGGG-3′; and GAPDH forward, 5′-CCTTCCGTGTCCCCACT-3′ and reverse, 5′-GCCTGCTTCACCACCTTC-3′. GAPDH expression was used as the internal control for normalization. The 2−ΔΔCq method was used for the quantification of the expression levels (23).

Western blot analysis

Total protein was extracted from the DU145, PC-3 and LNCaP cell lines using RIPA lysis buffer (Beyotime Institute of Biotechnology) and centrifuged at 12,000 × g for 20 min at 4°C. Total protein was quantified using a BCA protein assay kit (Beyotime Institute of Biotechnology) and 30 µg protein/lane was separated on 10–12% gels using SDS-PAGE at a constant voltage of 95 V. The separated proteins were subsequently transferred onto PVDF membranes (MilliporeSigma) and blocked with 5% skimmed milk at 25°C for 2 h. The membranes were then incubated overnight at 4°C with the following primary antibodies: Anti-PP2A (cat. no. 12675-2-AP; dilution, 1:500), anti-XIAP (cat. no. 66800-1-Ig; dilution, 1:5,000), anti-Bax (cat. no. 50599-2-Ig; dilution, 1:1,000) and anti-Bcl-2 (cat. no. 12789-1-AP; dilution, 1:1,000) (all ProteinTech Group, Inc.), anti-phosphorylated (p)-eIF4B (cat. no. R26284; dilution, 1:5,000; Chengdu Zen Bioscience Co., Ltd), anti-eIF4B (cat. no. R26713; dilution, 1:5,000; Chengdu Zen Bioscience Co., Ltd), anti-GAPDH (cat. no. AB0037; dilution, 1:3,000; Shanghai Abways Biotechnology Co., Ltd.;) and anti-cleaved caspase-3 (cat. no. 9664; dilution, 1:1,000; Cell Signaling Technology, Inc.). Following incubation with the primary antibodies, the membranes were incubated with an HRP-conjugated secondary antibody (cat. no. 91196; dilution, 1:2,000; Cell Signaling Technology, Inc.) at 25°C for 1 h. The protein bands were visualized using an ECL system (GelDoc Go; Bio-Rad Laboratories, Inc.). The blots were quantified using Evolution (version number:18.0.8.0, Viber Lourmat).

Flow cytometric analysis of apoptosis

Cell apoptosis (early + late apoptotic cells) was analyzed 48 h after treatment. LNCaP cells were transfected with siPP2A or si-NC (5 µl; 20 µM) at 37°C for 6 h in the presence or absence of subsequent 5 nmol/l docetaxel treatment. DU145 and PC-3 cells were treated with 10 µmol/l DT061 (dissolved in DMSO), 5 nmol/l docetaxel, 10 µmol/l DT061 (dissolved in DMSO) + 5 nmol/l docetaxel at 37°C for 48 h; the control group was treated with DMSO. The treated cells were subsequently trypsinized and resuspended in PBS, then stained using reagents from the Annexin V-FITC/PI Apoptosis Detection kit (cat. no. 556570; BD Biosciences), according to the manufacturer's protocol. CytoFLEX V2-B4-R0 Flow Cytometer (cat. no. C02944; Beckman Coulter) and CytExpert software were used for analysis (version no. 2.4.0.28; Beckman Coulter, Inc.).

Statistical analysis

All the experiments were performed three times. Statistical analysis was performed using SPSS v22.0 software (IBM Corp.) and the data are presented as the mean ± SD. Statistical differences between groups (unpaired) were determined using a Student's t-test or one-way ANOVA followed by Tukey's post hoc test. P<0.05 was considered to indicate a statistically significant difference.

Results

PP2A expression is decreased in CRPC cells

To determine the mRNA and protein expression level of PP2A in different prostate cancer cell lines, including LNCaP cells (sensitive to ADT), and the DU145 and PC-3 cells (insensitive to ADT), RT-qPCR and western blot analysis were performed, respectively. The mRNA expression levels of PP2A were significantly increased in LNCaP cells compared with those in the DU145 and PC-3 cell lines (Fig. 1A). Similarly, western blot analysis revealed that the protein expression levels of PP2A were also significantly increased in LNCaP cells compared with those in the DU145 and PC-3 cell lines (Fig. 1B). These results indicated that the expression level of PP2A was lower in AR-negative cell lines than AR-positive cell lines.

Figure 1. PP2A (A) mRNA and (B) protein expression levels in the LNCaP, DU145 and PC-3 cell lines. *P<0.05, **P<0.01 vs. LNCaP cell line. PP2A, serine/threonine protein phosphatase 2A.

Increase in PP2A expression promotes cell apoptosis and drug sensitivity to docetaxel

To investigate the biological role of PP2A in cell apoptosis and drug resistance, flow cytometry and CCK-8 assays were performed. The small molecule, DT061 (10 µmol/l; dissolved in DMSO), which is able to increase the population of PP2A heterotrimers (24), was used to upregulate PP2A expression levels in the CRPC cell lines, DU145 and PC-3 (Fig. 2A and B). The control group contained cells treated with DMSO. Flow cytometric analysis of apoptosis revealed that DT061 increased the apoptosis rate compared with the control (DMSO). Treatment with DT061 combined with docetaxel (5 nmol/l) significantly increased the apoptotic rate compared to the Docetaxel group (5 nmol/l) in both the DU145 and PC-3 cell lines (Fig. 2C and D). The results of western blot analysis demonstrated that the protein expression level of Bcl-2 was decreased in the DT061 group compared with that in the control group, while the expression levels of Bax and cleaved caspase-3 were increased in the DT061 group compared with those in the control group in both the DU145 and PC-3 cell lines (Fig. 2E and F). The results of the CCK-8 assay found that the CRPC cell lines (DU145 and PC-3) in the DT061 group had significantly increased sensitivity to docetaxel compared with the cell lines in the control group (Fig. 2G and H). These results indicated that DT061 may upregulate the expression levels of PP2A, which may promote cell apoptosis and drug sensitivity to docetaxel in the CRPC cell lines.

Figure 2. PP2A protein expression levels in the (A) DU145 and (B) PC-3 cells treated with DT061 were analyzed using western blot analysis. **P<0.01, ***P<0.001 vs. control. Apoptotic rate of (C) DU145 and (D) PC-3 cells following treatment with docetaxel and DT061 was analyzed using flow cytometry. *P<0.05, **P<0.01, ***P<0.001. (E) DU145 and (F) PC-3 cells were treated with DT061 and the protein expression levels of Bax, Bcl-2 and cleaved caspase-3 were analyzed using western blot analysis. *P<0.05, **P<0.01 vs. control. Viability of (G) DU145 and (H) PC-3 cells treated with DT061 was decreased compared with that in the control group. *P<0.05, **P<0.01, ***P<0.001 vs. control. PP2A, serine/threonine protein phosphatase 2A.

PP2A knockdown supresses cell apoptosis and enhances the tolerance to docetaxel

To further validate the role that PP2A may play in apoptosis, drug resistance and the development of prostate cancer, the LNCaP cell line was transfected with siPP2A to knock down its expression (Fig. 3A and B), then flow cytometry, western blot analysis and a CCK-8 assay were performed. Flow cytometric analysis of apoptosis found that knockdown of PP2A decreased the apoptotic rate in the LNCaP cells (Fig. 3C). The siRNA used in the transfection was siRNA2. The results of western blot analysis revealed that the expression level of Bcl-2 was increased in the siPP2A group compared with that in the si-NC group. By contrast, the expression levels of Bax and cleaved caspase-3 were decreased in the siPP2A group compared with those in the si-NC group (Fig. 3D).

Figure 3. PP2A (A) mRNA and (B) protein expression levels in the LNCaP cell line transfected with siPP2A. **P<0.01, ***P<0.001 vs. siNC. (C) Apoptotic rate of LNCaP cells treated with docetaxel and transfected with siPP2A was analyzed using flow cytometry. *P<0.05, **P<0.01, ***P<0.001. (D) Protein expression levels of Bax, Bcl-2 and cleaved caspase-3 in the LNCaP cell line transfected with siPP2A. *P<0.05 vs. siNC. (E) Cell viability in the cells transfected with siRNA was increased compared with that in the NC group. *P<0.05, **P<0.01, ***P<0.001 vs. NC. PP2A, serine/threonine protein phosphatase 2A; NC, negative control; si, small interfering RNA.

PP2A expression was knocked down in the LNCaP cells, which were then treated with docetaxel (0.5–500 nM) for 48 h, and cell viability was measured using a CCK-8 assay. The results demonstrated that the siPP2A group exhibited enhanced tolerance to docetaxel (Fig. 3E). These findings suggested that PP2A knockdown supresses cell apoptosis and enhances the tolerance to docetaxel.

XIAP expression is associated with the expression level of PP2A

To determine the association between PP2A and XIAP, PP2A expression was increased or knocked down, then western blot analysis was performed to determine changes in the protein expression levels of p-eIF4B and XIAP. In the DU145 and PC-3 cell lines, when DT061 was used to increase the expression level of PP2A, the protein expression levels of p-eIF4B and XIAP were found to be significantly decreased compared with those in the si-NC group (Fig. 4A-D). By contrast, when the expression level of PP2A was knocked down in the LNCaP cells using siPP2A, the protein expression levels of p-eIF4B and XIAP were increased compared with those in the si-NC group (Fig. 4E and F). These results indicated that the change in PP2A expression may regulate the expression level of XIAP via the PP2A/eIF4B/XIAP signaling pathway.

Figure 4. PP2A, p-eIF4B, eIF4B and XIAP protein expression levels in (A and B) DU145 and (C and D) PC-3 cells treated with DT061. *P<0.05, **P<0.01, ***P<0.001 vs. control. (E) PP2A, P-eIF4B/eIF4B, XIAP protein expression levels in the LNCaP cell line transfected with siPP2A and the results were subsequently (F) quantified using densitometry. *P<0.05, **P<0.01 vs. siNC. PP2A, serine/threonine protein phosphatase 2A; NC, negative control; si, small interfering RNA; p, phosphorylated; XIAP, X-linked inhibitor of apoptosis; eIF4B, eukaryotic initiation factor 4B.

Discussion

As the terminal stage of prostate cancer, CRPC has been associated with a high metastatic rate, chemotherapy resistance and poor survival rates. The median survival time of patients with CRPC was recorded as 8.6±10.6 in the Netherlands (25), 13.0 in the USA (26), 14.5 months in Italy (27). A previous study revealed that 83.8% of patients in Japan were shown to have metastases at diagnosis (28). Over the past 30 years, numerous potential drugs for CRPC have emerged, such as cabazitaxel (29,30), abiraterone acetate (31,32) and enzalutamide (33), rendering the treatment regimen of the disease more flexible and diverse. However, the curative effect of CRPC is far from satisfactory, particularly for patients with metastatic (m)CRPC (34). Significant effort has been made to improve the prognosis of these patients; however, efficient and effective therapies have not yet been developed (34). Unlike other types of cancer, such as bladder and kidney cancer, the dependence of prostate cancer on androgens for propagation and growth make it unique. Therefore, ADT is widely used in clinical practice and has been shown to be effective (35). CRPC is described as prostate cancer that has progressed despite ADT. However, to the best of our knowledge, the process through which prostate cancer cells become castrate-resistant is not yet completely understood. It has been suggested that ADT may inhibit the proliferation of androgen-dependent cells. This then allows androgen-independent cells to become the new dominant primary tumor cells (36). Another study has indicated that androgen receptor amplification and hypersensitivity/mutations may play a key role in this process (2). However, treatment for CRPC is difficult; therefore, it remains of utmost importance to understand the underlying mechanisms of CRPC development.

Accumulating data have demonstrated that PP2A activation is of great significance in prostate cancer. A previous study showed that PP2A activation could suppress prostate tumor growth and metastasis (37). PP2A activation inhibited the growth of androgen-independent prostate cancer cells (38). On the other hand, downregulation of PP2A enhanced metastatic ability and led to higher mortality in prostate cancer (39,40). These results indicate that PP2A activation is promising in the treatment of prostate cancer. The results of the present study found that the mRNA and protein expression levels of PP2A were decreased in prostate cancer cells, as the tumor cells transitioned from non-CRPC cells to CRPC cells. The knockdown of PP2A expression was subsequently found to promote CRPC cell chemoresistance and inhibit apoptosis. A previous study found that treatment with the PP2A activators, forskolin and FTY720, exerted antitumor effects and affected the proliferation of the PC-3 cell line (41). To determine the effect of activated PP2A on CRPC cells in the current study, the population of PP2A heterotrimers was increased by treatment with another PP2A activator, DT061 (11,24,42) in the DU145 and PC-3 cell lines. The results revealed that the CRPC cells exhibited higher apoptotic rates. In addition, the protein expression levels of the apoptosis-related proteins, Bax and cleaved caspase-3, were upregulated, while the protein expression level of Bcl-2 was downregulated. These results indicated that DT061 may regulate the expression level of apoptosis-related proteins to promote cell apoptosis. For patients with mCRPC, docetaxel remains the first-line treatment method (43). However, once resistance to docetaxel emerges, the therapeutic benefit is limited, which leads to therapeutic failure (2). In the present study, the results of the CCK-8 assay revealed that CRPC cells treated with DT061 showed an enhanced sensitivity to docetaxel. These results suggested that DT061 may ameliorate docetaxel resistance and be of potential benefit for patients with CRPC.

The functional loss of PP2A serves a key role in tumorigenesis. For example, a previous study found that protein expression levels of PP2A-Aa and PP2A-Ba are markedly decreased in breast cancer tissue and the knockdown of PP2A-Ba enhances proliferation in MCF7 breast cancer cells (44). PP2A complexes consist of structural (PP2A-A), regulatory (PP2A-B), and catalytic (PP2A-C) subunits (24). The PP2A subunits may vary in different cell lines, which may cause the PP2A protein to exhibit split bands when examined using western blot analysis. In the present study, to further investigate the roles that PP2A played in the progression of prostate cancer and its association with apoptosis and chemoresistance, siPP2A was transfected into the AR-positive cell line, LNCaP. The results revealed that the apoptotic rate was decreased following the knockdown of PP2A expression, which indicated that PP2A knockdown may play a vital role in the promotion of cell propagation. Similarly, the results of the CCK-8 assay revealed that the transfection of siPP2A into the LNCaP cell line increased the resistance of the cells to docetaxel. These results suggested that the knockdown of PP2A may decrease the curative effect of docetaxel.

The activation of PP2A has been considered as a promising therapeutic strategy in various types of cancer, including acute myeloid leukemia (45), KRAS-mutant lung cancer (46) and prostate cancer (47); however, to the best of our knowledge, the underlying mechanism of action of PP2A has not been fully determined. Previous studies revealed that a PP2A agonist increased the levels of apoptosis by downregulating cellular inhibitor of PP2A expression levels (48,49). Another study revealed that PP2A activation downregulated the phosphoproteome and weakened the stability of the androgen receptor in CRPC (50). The findings of the current study revealed that, when the expression level of PP2A was increased, the protein expression levels of p-eIF4B and XIAP were decreased. By contrast, when PP2A expression was knocked down, p-eIF4B and XIAP protein expression levels were increased. These results indicated that XIAP may be a downstream factor of PP2A and that the PP2A/p-eIF4B/XIAP signaling pathway may participate in the development of prostate cancer. There are numerous apoptosis-related pathways that are modulated or mediated by PP2A. For example, the PP2A activator, FTY720, was able to induce ferroptosis and promote multiple myeloma cell apoptosis by activating the PP2A/AMP-activated protein kinase pathway (51). In addition, PP2A was able to regulate the ERK, p38 MAPK and Akt signaling pathways to enhance apoptosis in lung cancer cells (52). However, to the best of our knowledge, whether DT061 affects these pathways remains undetermined, and further research is required to investigate the effect of PP2A activation induced by DT061. Furthermore, only in vitro not in vivo experiments were performed, which is a limitation to the present study. PP2A knockdown is known to play a key role in malignant cell proliferation and drug resistance (44). However, few studies have revealed the effect of PP2A knockdown on apoptosis and docetaxel resistance in prostate cancer. In a previous study, a longer overall survival time was observed in patients with mCRPC when treated with docetaxel compared with that in patients treated with mitoxantrone; however, docetaxel therapy was limited as a result of the emergence of tumor resistance (53). There have been numerous explanations underlying the emergence of docetaxel resistance, including the overexpression of multidrug resistance genes, tubulin alterations, the presence of androgen receptor variants and the occurrence of epithelial-mesenchymal transition (53). In the present study, XIAP protein expression levels were found to be regulated by PP2A; however, the mechanism by which the altered expression of XIAP resulted in docetaxel resistance remains unclear. A previous study found that downregulated protein expression levels of XIAP was associated with drug resistance in the DU145 cell line (54). XIAP inhibition led to an increase in caspase-3 activity and decreased cell viability, which rendered CRPC cells more sensitive to chemotherapy (54). Therefore, we hypothesized that the anti-apoptotic effect of XIAP may enhance the viability of CRPC cells and result in docetaxel resistance.

In conclusion, the findings of the current study indicated that PP2A may play a vital role in the development of CRPC. PP2A was discovered to decrease XIAP protein expression levels via the PP2A/p-eIF4B/XIAP signaling pathway, which promoted apoptosis and improved cell resistance to docetaxel. Therefore, the activation of PP2A may represent a novel therapeutic approach for the treatment of CRPC.

Acknowledgements

Not applicable.

Funding

The present study was supported by a grant from the Chongqing Basic Science and Advanced Technology Research Program (grant no. cstc2017jcyjAX0049).

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Authors' contributions

WH and SY contributed to the conception and design of the study. SY and HT performed the experiments. JZ and ZQ collected the data. JZ and ZQ confirm the authenticity of all the raw data. TL, JZ, ZQ and YC performed the statistical analysis. SY wrote the first draft of the manuscript. SY, YC and HT contributed to the writing of the manuscript. All authors have read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References