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Article

Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer

  • Authors:
    • Teng Wang
    • Kuan Ning
    • Ting-Xun Lu
    • Dong Hua
  • View Affiliations / Copyright

    Affiliations: Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215004, P.R. China, Department of Oncology, Affiliated Hospital of Jiangnan University and the Fourth People's Hospital of Wuxi, Wuxi, Jiangsu 214062, P.R. China
  • Pages: 1059-1065
    |
    Published online on: December 15, 2016
       https://doi.org/10.3892/or.2016.5322
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Abstract

Reprogramming of energy metabolism (aerobic glycolysis) is thought to play an essential role in cancer. Compared to oxidative phosphorylation, aerobic glycolysis consumes more glucose through the upregulation of glucose transporters, notably glucose transporter 1 (GLUT1). Elevated glycolysis occurs in chemoresistant cancer cells, but the detailed mechanism is not well understood. The upregulation of the Ca2+-permeable transient receptor potential channel 5 (TrpC5) activates the Wnt/β-catenin signaling pathway in 5-fluorouracil (5-Fu)-resistant human colorectal cancer (CRC) HCT-8 (HCT-8/5-Fu) cells. In the present study, TrpC5 was overexpressed at the mRNA and protein levels along with GLUT1 in HCT-8/5-Fu cells. Suppression of TrpC5 expression with a TrpC5-specific shRNA reduced the induction of GLUT1 in the HCT-8 cells. The inhibition of the Wnt/β-catenin signaling pathway with XAV939 resulted in a decreased GLUT1 and nuclear c-Myc expression. Further study using clinical specimens validated the positive correlation between TrpC5 and GLUT1 protein levels and showed that a high TrpC5/GLUT1 expression was significantly correlated with chemoresistance. Taken together, we demonstrated the essential role of TrpC5 in GLUT1 induction and revealed that a high TrpC5/GLUT1 expression is associated with chemoresistance in human CRC.
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Copy and paste a formatted citation
Spandidos Publications style
Wang T, Ning K, Lu T and Hua D: Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer. Oncol Rep 37: 1059-1065, 2017.
APA
Wang, T., Ning, K., Lu, T., & Hua, D. (2017). Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer. Oncology Reports, 37, 1059-1065. https://doi.org/10.3892/or.2016.5322
MLA
Wang, T., Ning, K., Lu, T., Hua, D."Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer". Oncology Reports 37.2 (2017): 1059-1065.
Chicago
Wang, T., Ning, K., Lu, T., Hua, D."Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer". Oncology Reports 37, no. 2 (2017): 1059-1065. https://doi.org/10.3892/or.2016.5322
Copy and paste a formatted citation
x
Spandidos Publications style
Wang T, Ning K, Lu T and Hua D: Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer. Oncol Rep 37: 1059-1065, 2017.
APA
Wang, T., Ning, K., Lu, T., & Hua, D. (2017). Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer. Oncology Reports, 37, 1059-1065. https://doi.org/10.3892/or.2016.5322
MLA
Wang, T., Ning, K., Lu, T., Hua, D."Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer". Oncology Reports 37.2 (2017): 1059-1065.
Chicago
Wang, T., Ning, K., Lu, T., Hua, D."Elevated expression of TrpC5 and GLUT1 is associated with chemoresistance in colorectal cancer". Oncology Reports 37, no. 2 (2017): 1059-1065. https://doi.org/10.3892/or.2016.5322
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