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HMGB1-mediated autophagy modulates sensitivity of colorectal cancer cells to oxaliplatin via MEK/ERK signaling pathway

机译:HMGB1介导的自噬通过MEK / ERK信号通路调节结直肠癌细胞对奥沙利铂的敏感性

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摘要

In the present study, we examined the mechanisms of oxaliplatin-induced drug resistance in human colorectal cancer cell lines HT29 and HCT116. Our results demonstrate a significant autophagy expression in CRC cells after an oxaliplatin treatment. Administration of oxaliplatin to human CRC cells significantly enhanced the expression of HMGB1, which regulated the autophagy response and negatively regulate the cell apoptosis. Moreover, a decreased oxaliplatin -induced autophagy response and an increased apoptosis level were detected in stable CRC cells harboring HMGB1 shRNA. Then we noted that HMGB1 significantly induced extracellular signal-regulated kinase (ERK)/Extracellular signal-regulated kinase kinase (MEK) phosphorylation. Taken together, these data suggest that HMGB1-mediated autophagy modulates sensitivity of colorectal cancer cells to oxaliplatin via MEK/ERK signaling pathway.
机译:在本研究中,我们研究了奥沙利铂诱导人结肠直肠癌细胞系HT29和HCT116耐药的机制。我们的结果表明,在奥沙利铂治疗后,CRC细胞中有明显的自噬表达。奥沙利铂对人CRC细胞的给药显着增强了HMGB1的表达,从而调节了自噬反应并负调节了细胞凋亡。此外,在带有HMGB1 shRNA的稳定CRC细胞中检测到了奥沙利铂诱导的自噬反应降低和凋亡水平升高。然后,我们注意到HMGB1显着诱导细胞外信号调节激酶(ERK)/细胞外信号调节激酶激酶(MEK)磷酸化。综上所述,这些数据表明,HMGB1介导的自噬通过MEK / ERK信号通路调节大肠癌细胞对奥沙利铂的敏感性。

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