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Article

β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells

  • Authors:
    • Li Shen
    • Xiaoxia Dong
    • Yingying Wang
    • Li Qiu
    • Feng Peng
    • Zhiguo Luo
  • View Affiliations / Copyright

    Affiliations: Department of Clinical Oncology, Taihe Hospital, Hubei University of Medicine, Shiyan, Hubei 442000, P.R. China, Department of Biochemistry, School of Basic Medical Sciences, Hubei University of Medicine, Shiyan, Hubei 442000, P.R. China, 2014 Biological Sciences, School of Biomedical Engineering, Hubei University of Medicine, Shiyan, Hubei 442000, P.R. China
  • Pages: 2006-2014
    |
    Published online on: February 1, 2018
       https://doi.org/10.3892/or.2018.6243
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Abstract

Correlations between drug resistance and glycosylation changes have been analyzed intensively in the field of tumor biology. The present study was aimed to investigate the glycan and glycogene alterations involved in oxaliplatin resistance in human colon cancer cells. Using the lectin microarray for glycan composition and FITC-lectin binding for glycan profiling, we found that polylactosamine-type N-glycans were significantly increased in oxaliplatin-resistant SW620R cells. Using real-time PCR for quantification of glycogenes, we targeted β-1,3-N-acetylglucosaminyltransferase 8 (β3GnT8), which was overexpressed in SW620R cells. Using an RNA interference strategy, we revealed that the silencing of β3GnT8 in SW620R cells resulted in increased chemosensitivity to oxaliplatin. Conversely, the engineered overexpression of β3GnT8 in SW620 cells enhanced resistance to oxaliplatin. Further data revealed that manipulation of β3GnT8 was able to modify polylactosamine chains on integrin β1 and to regulate the integrin β1 downstream signaling pathway. These results revealed that β3GnT8 may play a key role in the development of oxaliplatin resistance in colon cancer cells possibly through the alteration of the glycosylation of integrin β1. These findings may be valuable for overcoming drug resistance in colon cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Shen L, Dong X, Wang Y, Qiu L, Peng F and Luo Z: β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells. Oncol Rep 39: 2006-2014, 2018.
APA
Shen, L., Dong, X., Wang, Y., Qiu, L., Peng, F., & Luo, Z. (2018). β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells. Oncology Reports, 39, 2006-2014. https://doi.org/10.3892/or.2018.6243
MLA
Shen, L., Dong, X., Wang, Y., Qiu, L., Peng, F., Luo, Z."β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells". Oncology Reports 39.4 (2018): 2006-2014.
Chicago
Shen, L., Dong, X., Wang, Y., Qiu, L., Peng, F., Luo, Z."β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells". Oncology Reports 39, no. 4 (2018): 2006-2014. https://doi.org/10.3892/or.2018.6243
Copy and paste a formatted citation
x
Spandidos Publications style
Shen L, Dong X, Wang Y, Qiu L, Peng F and Luo Z: β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells. Oncol Rep 39: 2006-2014, 2018.
APA
Shen, L., Dong, X., Wang, Y., Qiu, L., Peng, F., & Luo, Z. (2018). β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells. Oncology Reports, 39, 2006-2014. https://doi.org/10.3892/or.2018.6243
MLA
Shen, L., Dong, X., Wang, Y., Qiu, L., Peng, F., Luo, Z."β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells". Oncology Reports 39.4 (2018): 2006-2014.
Chicago
Shen, L., Dong, X., Wang, Y., Qiu, L., Peng, F., Luo, Z."β3GnT8 regulates oxaliplatin resistance by altering integrin β1 glycosylation in colon cancer cells". Oncology Reports 39, no. 4 (2018): 2006-2014. https://doi.org/10.3892/or.2018.6243
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