虫草素抑制YAP/TAZ信号通路降低黑色素瘤细胞化疗耐药性

    Effect of Cordycepin on Chemotherapy Resistance of Melanoma Cells by Regulating the Hippo/YAP/TAZ Signaling Pathway

    • 摘要:
      目的 探究虫草素(cordycepin,Cor)调节Yes相关蛋白(Yes associated protein,YAP)/PDZ结合域的转录共刺激因子(transcriptional coactivator with PDZ-binding motif,TAZ)信号通路对黑色素瘤细胞化疗耐药性的影响。
      方法 以不同浓度顺铂(cisplatin,DDP)或Cor处理黑色素瘤A375细胞和A375/DDP细胞,CCK-8法检测细胞活力;将A375/DDP细胞分为对照组、DDP组、DDP+Cor组、DDP+XMU-MP-1组、DDP+Cor+XMU-MP-1组,检测各组细胞集落形成,Transwell检测侵袭,划痕实验检测迁移,流式细胞术检测凋亡,Western blot检测Bax、Bcl-2、MMP-2、YAP、MST1、TAZ蛋白表达。
      结果 不同浓度DDP处理后,A375细胞活力低于A375/DDP细胞(P<0.05),选取33.0 μmol/L DDP进行实验;A375/DDP细胞在不同浓度Cor处理下细胞活力逐渐降低(P<0.05),选取200 μmol/L作为后续Cor的实验浓度。与对照组相比,DDP组、DDP+Cor组细胞集落形成数、侵袭数、划痕愈合率、YAP、MST1、TAZ、Bcl-2、MMP-2蛋白表达下降,凋亡率、Bax表达升高(P<0.05);与DDP组相比,DDP+Cor组各指标趋势一致,DDP+XMU-MP-1组各指标趋势相反,且差异均显著(P<0.05);XMU-MP-1逆转Cor对A375/DDP增殖、迁移的抑制作用。
      结论 Cor可能通过抑制YAP/TAZ信号通路蛋白的表达,抑制细胞增殖、迁移和侵袭,促进凋亡,降低了黑色素瘤细胞的DDP耐药性。

       

      Abstract:
      Objective To investigate the effect of cordycepin (Cor) on the chemotherapy resistance of melanoma cells by regulating the Hippo/Yes associated protein (YAP) /transcriptional coactivator with PDZ binding motif (TAZ) signaling pathway.
      Methods Melanoma A375 cells and A375/ cisplatin (DDP) cells were treated with different concentrations of DDP or Cor, and cell viability was measured by CCK-8 method. A375/DDP cells were separated into control group, DDP group, DDP+Cor group, DDP+XMU-MP-1 group, and DDP+Cor+XMU-MP-1 group, cell colony formation in each group was detected, Transwell was applied to detect invasion, scratch experiment was applied to detect migration, flow cytometry was applied to detect apoptosis, Western blot was applied to detect the expression of Bax, Bcl-2, MMP-2, YAP, MST1, and TAZ proteins.
      Results After DDP treatment, the viability of A375 cell was lower than A375/DDP cells (P<0.05), 33.0 μmol/L DDP was selected for the experiment; A375/DDP cells showed a gradual decrease in cell viability under different concentrations of Cor treatment (P<0.05), 200 μmol/L were selected as the experimental concentration for subsequent Cor. Compared with the control group, the number of colony formation, invasion, scratch healing rate, and the expression of YAP, MST1, TAZ, Bcl-2, and MMP-2 proteins in DDP group and DDP+Cor group significantly decreased, the apoptosis rate and Bax expression significantly increased (P<0.05). Compared with the DDP group, the trend of all indexes in DDP+Cor group was consistent, while the trend of all indexes in DDP+XMU-MP-1 group was opposite, and the differences were significant (P<0.05); XMU-MP-1 reversed the inhibitory effect of Cor on proliferation and migration of A375/DDP.
      Conclusion Cor may inhibit the expression of YAP/TAZ signaling pathway proteins, inhibit cell proliferation, migration, and invasion, promote apoptosis, and reduce DDP resistance in melanoma cells.

       

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