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April 2012 Volume 27 Issue 4

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International Journal of Molecular Medicine is an international journal devoted to molecular mechanisms of human disease.

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International Journal of Oncology is an international journal devoted to oncology research and cancer treatment.

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Article

CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells

  • Authors:
    • Jian-Hua Yu
    • Xiang-Yu Zhong
    • Wei-Guang Zhang
    • Zhi-Dong Wang
    • Qin Dong
    • Sheng Tai
    • Hui Li
    • Yun-Fu Cui
  • View Affiliations / Copyright

    Affiliations: Department of Hepato­pancreatobiliary Surgery, Second Affiliated Hospital of Harbin Medical University, Harbin 150086, P.R. China, Department of Biochemistry and Molecular Biology, Basic Medical Science College, Harbin Medical University, Harbin 150081, P.R. China
  • Pages: 1266-1276
    |
    Published online on: December 30, 2011
       https://doi.org/10.3892/or.2011.1617
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Abstract

Cyclin-dependent kinase 10 (CDK10) is a member of the Cdc2 family of kinases, and has been demonstrated to be an important determinant of resistance to endocrine therapy for breast cancer. To investigate the expression and possible function of CDK10 in biliary tract cancer (BTC), we systematically examined CDK10 in tissues and cell lines. We found that expression of CDK10 was downregulated in both biliary tract tumors and cell lines. Remarkably, the expression of CDK10 correlated with clinical characteristics. Overexpression or knockdown of CDK10, respectively, inhibited or promoted cell proliferation, colony formation and migration. This suggests that CDK10 functions as a tumor suppressor gene in BTC. Overexpression of CDK10 caused malignant cells to become sensitive to chemotherapy and other hostile environments, suggesting that CDK10 functions to regulate survivability of BTC cells. We investigated the expression of six genes to resolve the mechanism. c-RAF was negatively regulated by CDK10 in both cells and specimens. Our results indicate that CDK10 plays a crucial role in the growth and survivability of biliary tract cancer, and offers a potential therapeutic target for this fatal disease.
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Copy and paste a formatted citation
Spandidos Publications style
Yu J, Zhong X, Zhang W, Wang Z, Dong Q, Tai S, Li H and Cui Y: CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells. Oncol Rep 27: 1266-1276, 2012.
APA
Yu, J., Zhong, X., Zhang, W., Wang, Z., Dong, Q., Tai, S. ... Cui, Y. (2012). CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells. Oncology Reports, 27, 1266-1276. https://doi.org/10.3892/or.2011.1617
MLA
Yu, J., Zhong, X., Zhang, W., Wang, Z., Dong, Q., Tai, S., Li, H., Cui, Y."CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells". Oncology Reports 27.4 (2012): 1266-1276.
Chicago
Yu, J., Zhong, X., Zhang, W., Wang, Z., Dong, Q., Tai, S., Li, H., Cui, Y."CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells". Oncology Reports 27, no. 4 (2012): 1266-1276. https://doi.org/10.3892/or.2011.1617
Copy and paste a formatted citation
x
Spandidos Publications style
Yu J, Zhong X, Zhang W, Wang Z, Dong Q, Tai S, Li H and Cui Y: CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells. Oncol Rep 27: 1266-1276, 2012.
APA
Yu, J., Zhong, X., Zhang, W., Wang, Z., Dong, Q., Tai, S. ... Cui, Y. (2012). CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells. Oncology Reports, 27, 1266-1276. https://doi.org/10.3892/or.2011.1617
MLA
Yu, J., Zhong, X., Zhang, W., Wang, Z., Dong, Q., Tai, S., Li, H., Cui, Y."CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells". Oncology Reports 27.4 (2012): 1266-1276.
Chicago
Yu, J., Zhong, X., Zhang, W., Wang, Z., Dong, Q., Tai, S., Li, H., Cui, Y."CDK10 functions as a tumor suppressor gene and regulates survivability of biliary tract cancer cells". Oncology Reports 27, no. 4 (2012): 1266-1276. https://doi.org/10.3892/or.2011.1617
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