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Article

Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers

  • Authors:
    • Zhao‑Wei Zou
    • Hai‑Jin Chen
    • Jin‑Long Yu
    • Zong‑Hai Huang
    • Shun Fang
    • Xiao‑Hua Lin
  • View Affiliations / Copyright

    Affiliations: Department of General Surgery, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, P.R. China, Department of Pathology, Zhujiang Hospital, Southern Medical University, Guangzhou, Guangdong 510282, P.R. China
  • Pages: 4893-4900
    |
    Published online on: October 6, 2016
       https://doi.org/10.3892/mmr.2016.5812
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Abstract

Chemotherapy is one of the most commonly used therapeutic strategies for metastatic colon cancer. However, the development of resistance to chemotherapeutic agents limits their application in clinical use. The underlying mechanisms of this resistance development require further elucidation. The current study investigated the effects of connexin43 (Cx43) gap junctions on 5‑fluorouracil (5‑FU), oxaliplatin and irinotecan in colon cancer cells. Three different methods were used to manipulate Cx43 gap junction function: i) Cell culture at different densities; ii) pretreatment with a Cx43 specific inhibitor or enhancer; and iii) Cx43 gene knock‑down. Results indicated that the cell toxicity of 5‑FU, oxaliplatin and irinotecan was cell density‑dependent, which was mediated by gap junctions. Downregulation of Cx43 gap junction functioning attenuated 5‑FU, oxaliplatin and irinotecan toxicity in colon cancer cells, which was increased in cells treated with a Cx43 gap junction function enhancer. Thus, the results of the present study suggest that resistance to 5‑FU, oxaliplatin and irinotecan in colon cancer cells was relative to Cx43 expression loss as cancer developed, which may indicate a novel basis for therapeutic strategy development to combat drug resistance in numerous cell types, in addition to colon cancer cells.
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Copy and paste a formatted citation
Spandidos Publications style
Zou ZW, Chen HJ, Yu JL, Huang ZH, Fang S and Lin XH: Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers. Mol Med Rep 14: 4893-4900, 2016.
APA
Zou, Z., Chen, H., Yu, J., Huang, Z., Fang, S., & Lin, X. (2016). Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers. Molecular Medicine Reports, 14, 4893-4900. https://doi.org/10.3892/mmr.2016.5812
MLA
Zou, Z., Chen, H., Yu, J., Huang, Z., Fang, S., Lin, X."Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers". Molecular Medicine Reports 14.5 (2016): 4893-4900.
Chicago
Zou, Z., Chen, H., Yu, J., Huang, Z., Fang, S., Lin, X."Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers". Molecular Medicine Reports 14, no. 5 (2016): 4893-4900. https://doi.org/10.3892/mmr.2016.5812
Copy and paste a formatted citation
x
Spandidos Publications style
Zou ZW, Chen HJ, Yu JL, Huang ZH, Fang S and Lin XH: Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers. Mol Med Rep 14: 4893-4900, 2016.
APA
Zou, Z., Chen, H., Yu, J., Huang, Z., Fang, S., & Lin, X. (2016). Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers. Molecular Medicine Reports, 14, 4893-4900. https://doi.org/10.3892/mmr.2016.5812
MLA
Zou, Z., Chen, H., Yu, J., Huang, Z., Fang, S., Lin, X."Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers". Molecular Medicine Reports 14.5 (2016): 4893-4900.
Chicago
Zou, Z., Chen, H., Yu, J., Huang, Z., Fang, S., Lin, X."Gap junction composed of connexin43 modulates 5‑fluorouracil, oxaliplatin and irinotecan resistance on colorectal cancers". Molecular Medicine Reports 14, no. 5 (2016): 4893-4900. https://doi.org/10.3892/mmr.2016.5812
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