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Antagonism of miRNA-21 Sensitizes Human Gastric Cancer Cells to Paclitaxel

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Abstract

The development of drug resistance has largely limited the clinical outcome of anti-cancer treatment. Recent work has highlighted the involvement of non-coding RNAs, microRNAs (miRNAs), in cancer development. The present study aimed to investigate the role of miR-21 in the development of drug resistance to paclitaxel in gastric cancer cells. Our study found that the expression of miR-21 upregulated in the paclitaxel resistant cell line SGC7901/paclitaxel compared to its parental line SGC7901. Moreover, over-expression of miR-21 significantly decreased antiproliferative effects and apoptosis induced by paclitaxel, while knockdown of miR-21 dramatically increased antiproliferative effects and apoptosis induction by paclitaxel. Moreover, our results demonstrated that miR-21 may modulate the sensitivity to PTX, at least in part, by regulating the expression of P-glycoprotein.

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Acknowledgments

The research is supported by Innovation Fund of Xinjiang Medical University (Fund No. XJC201264) and Innovation Fund of The Third Affiliated Hospital (Xinjiang Tumor Hospital), Xinjiang Medical University (Fund No. SLCX0304).

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Correspondence to Bo Jin or Yanping Liu.

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Jin, B., Liu, Y. & Wang, H. Antagonism of miRNA-21 Sensitizes Human Gastric Cancer Cells to Paclitaxel. Cell Biochem Biophys 72, 275–282 (2015). https://doi.org/10.1007/s12013-014-0450-2

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