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17-AAG通过抑制Erk信号通路增强奥沙利铂诱导结肠癌细胞凋亡[J]. 肿瘤防治研究, 2013, 40(08): 752-757. DOI: 10.3971/j.issn.1000-8578.2013.08.007
引用本文: 17-AAG通过抑制Erk信号通路增强奥沙利铂诱导结肠癌细胞凋亡[J]. 肿瘤防治研究, 2013, 40(08): 752-757. DOI: 10.3971/j.issn.1000-8578.2013.08.007
17-Allylamino-17-demethoxygeldanamycin Enhances Apoptosis Induced by Oxaliplatin via Suppression of Erk Signaling Pathway in RKO Colon Cancer Cell Line[J]. Cancer Research on Prevention and Treatment, 2013, 40(08): 752-757. DOI: 10.3971/j.issn.1000-8578.2013.08.007
Citation: 17-Allylamino-17-demethoxygeldanamycin Enhances Apoptosis Induced by Oxaliplatin via Suppression of Erk Signaling Pathway in RKO Colon Cancer Cell Line[J]. Cancer Research on Prevention and Treatment, 2013, 40(08): 752-757. DOI: 10.3971/j.issn.1000-8578.2013.08.007

17-AAG通过抑制Erk信号通路增强奥沙利铂诱导结肠癌细胞凋亡

17-Allylamino-17-demethoxygeldanamycin Enhances Apoptosis Induced by Oxaliplatin via Suppression of Erk Signaling Pathway in RKO Colon Cancer Cell Line

  • 摘要: 目的 研究17-AAG与奥沙利铂是否存在协同效应,并探讨PI3K/Akt、Erk信号通路在奥沙利铂联合17-AAG诱导人结肠癌细胞凋亡过程中的作用。方法 四甲基偶氮唑盐比色实验(MTT法)检测17-AAG、奥沙利铂对细胞增殖的抑制作用;流式细胞术分析细胞凋亡情况;Western blot法检测相关蛋白的表达水平。结果 17-AAG能抑制RKO细胞的增殖;17-AAG联合奥沙利铂作用于RKO细胞24 h后,G2/M期细胞比例及凋亡率明显增加;奥沙利铂抑制p-Akt、p-Erk的活化,上调Bax,下调Bcl-2蛋白表达,活化裂解Caspase-3,联合使用17-AAG后可进一步增强上述作用,但对PI3K/Akt信号通路影响不大。结论 本实验表明17-AAG具有增强奥沙利铂诱导结肠癌RKO细胞凋亡的作用,同时也说明17-AAG与奥沙利铂存在协同效应;17-AAG上调Bax,下调Bcl-2蛋白表达及增强奥沙利铂对Erk信号通路的抑制作用可能是其促进凋亡的重要机制之一。

     

    Abstract: Objective To determine whether there was a synergistic effect between the Hsp90 inhibitor 17-AAG and oxaliplatin and to further investigate the roles of PI3K/Akt and Erk in apoptosis induced with 17-AAG and oxaliplatin treatment in a human colon cancer cell line. Methods Colorimetric 3-4, 5-dimethy thiazol-2-yl-2,5-diphenyl tetrazolium bromide (MTT) assay was used to study the inhibitory effect on proliferation of RKO cell treated with 17-AAG and oxaliplatin,Apoptosis was evaluated by flow cytometry;Western blot was carried out to determine protein expression levels. Results 17-AAG could definitely inhibit the of RKO cells. When the RKO cells were exposed to 17-AAG combined with oxaliplatin for 24 h, G2/M ratio and apoptosis rates were significantly increased. Oxaliplatin significantly decreased the protein expression of p-Akt and p-Erk. Oxaliplatin was also found to significantly increase the protein expression of Bax and Caspase-3 and to decrease the expression of Bcl-2. All these effects were enhanced when identical experiments were carried out in the presence of 17-AAG, but it had no apparent effects on the PI3K/Akt signaling pathway. Conclusion 17-AAG enhances apoptosis induced by oxaliplatin in RKO cells and there maybe exist a synergistic effect between 17-AAG and oxaliplatin. The increased expression of Bax, the decreased expression of Bcl-2 and the inhibition of Erk signaling pathway may be the underlying mechanisms leading to apoptosis.

     

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