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CJAP ›› 2017, Vol. 33 ›› Issue (4): 289-293.doi: 10.12047/j.cjap.5559.2017.071

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Silencing of PKG1 expression enhances the efficacy of vemurafenib against melanoma cell

LIU Rong, WAN Xin, WANG Xi, LI Fan-lu, JING Jia-ni, CUI Xiang-li   

  1. Department of Physiology, Cell Physiology Key Laboratory of Shanxi Province, Shanxi Medical University, Taiyuan 030001, China
  • Received:2017-01-17 Revised:2017-05-13 Online:2017-07-28 Published:2018-06-19
  • Supported by:
    国家自然科学基金(81272695);山西省自然科学基金(2012011040-8);山西医科大学科技创新基金([2012]11)

Abstract: Objective: To explore whether targeting phosphoglycerate kinase 1 (PGK1) can enhance the sensitivity of BRAFV600E mutation melanoma cells to vemurafenib.Methods: The methods of cell biology, molecular biology and pharmacology(MTT assay, Western blot, FCM, Colongenic assay) were used in this study.Results: ① Silencing of PGK1 expression increased the efficacy of vemurafenib in melanoma cells, as evidenced by greater killing in the tumor cells subjected to combined treatment of vemurafenib with siPGK1; ②The mechanism of enhanced sensitivity of melanoma cells to vemurafenib was associated with activation of apoptotic signaling pathway.Conclusion: Targeting of PGK1 may represent a novel strategy of sensitizing melanoma cells to vemurafinib.

Key words: melanoma, PGK1, vemurafenib, apoptosis

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