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Article

Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy

  • Authors:
    • Shuang Qiu
    • Liang Sun
    • Ye Jin
    • Qi An
    • Changjiang Weng
    • Jianhua Zheng
  • View Affiliations / Copyright

    Affiliations: Department of Obstetrics and Gynecology, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China, Department of General Surgery, The First Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang 150001, P.R. China, State Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Research Institute of the Chinese Academy of Agricultural Sciences, Harbin, Heilongjiang 150001, P.R. China
  • Pages: 309-316
    |
    Published online on: June 6, 2017
       https://doi.org/10.3892/or.2017.5706
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Abstract

Ovarian cancer is the most lethal disease among all gynecological malignancies. Interval cytoreductive surgery and cisplatin‑based chemotherapy are the recommended therapeutic strategies. However, acquired resistance to cisplatin remains a big challenge for the overall survival and prognosis in ovarian cancer. Complicated molecular mechanisms are involved in the process. At present, increasing evidence indicates that autophagy plays an important role in the prosurvival and resistance against chemotherapy. In the present study, as a novel autophagy regulator, BCL2‑associated athanogene 3 (BAG3) was investigated to study its role in cisplatin sensitivity in epithelial ovarian cancer. However, whether BAG3 participates in cisplatin sensitivity by inducing autophagy and the underlying mechanism in ovarian cancer cells remain to be clarified. Through the use of quantitative real-time PCR, western blot analysis, CCK-8 and immunofluorescence assays our data revealed that cisplatin-induced autophagy protected ovarian cancer cells from the toxicity of the drug and that this process was regulated by BAG3. Silencing of BAG3 increased cisplatin-induced apoptosis. The results also revealed BAG3 as a potential therapeutic target which enhanced the efficacy of cisplatin in ovarian cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Qiu S, Sun L, Jin Y, An Q, Weng C and Zheng J: Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy. Oncol Rep 38: 309-316, 2017.
APA
Qiu, S., Sun, L., Jin, Y., An, Q., Weng, C., & Zheng, J. (2017). Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy. Oncology Reports, 38, 309-316. https://doi.org/10.3892/or.2017.5706
MLA
Qiu, S., Sun, L., Jin, Y., An, Q., Weng, C., Zheng, J."Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy". Oncology Reports 38.1 (2017): 309-316.
Chicago
Qiu, S., Sun, L., Jin, Y., An, Q., Weng, C., Zheng, J."Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy". Oncology Reports 38, no. 1 (2017): 309-316. https://doi.org/10.3892/or.2017.5706
Copy and paste a formatted citation
x
Spandidos Publications style
Qiu S, Sun L, Jin Y, An Q, Weng C and Zheng J: Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy. Oncol Rep 38: 309-316, 2017.
APA
Qiu, S., Sun, L., Jin, Y., An, Q., Weng, C., & Zheng, J. (2017). Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy. Oncology Reports, 38, 309-316. https://doi.org/10.3892/or.2017.5706
MLA
Qiu, S., Sun, L., Jin, Y., An, Q., Weng, C., Zheng, J."Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy". Oncology Reports 38.1 (2017): 309-316.
Chicago
Qiu, S., Sun, L., Jin, Y., An, Q., Weng, C., Zheng, J."Silencing of BAG3 promotes the sensitivity of ovarian cancer cells to cisplatin via inhibition of autophagy". Oncology Reports 38, no. 1 (2017): 309-316. https://doi.org/10.3892/or.2017.5706
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