Mitchell Cancer Institute, University of South Alabama, Mobile, Alabama 36604, USA.
J Biol Chem. 2013 Feb 8;288(6):4334-45. doi: 10.1074/jbc.M112.419168. Epub 2012 Dec 19.
Chemoresistance is a major obstacle in cancer treatment. Our previous studies have shown that miR-125b plays an important role in chemoresistance. Here we report a novel mechanism that up-regulation of miR-125b through Wnt signaling by Snail enriches cancer stem cells. Overexpression of Snail dramatically increases the expression of miR-125b through the Snail-activated Wnt/β-catenin/TCF4 axis. Snail confers chemoresistance by repressing Bak1 through up-regulation of miR-125b. Restoring the expression of Bak1 or depleting miR-125b re-sensitizes Snail-expressing cancer cells to Taxol, indicating that miR-125b is critical in Snail-induced chemoresistance. Moreover, overexpression of miR-125b significantly increases the cancer stem cell population (CD24-CD44+), while depletion of miR-125b or rescue of the expression of Bak1 increases the non-stem cell population (CD24+CD44+) in Snail-overexpressing cells. These findings strongly support that miR-125b functions as a key mediator in Snail-induced cancer stem cell enrichment and chemoresistance. This novel mechanism for Snail-induced stem cell propagation and chemoresistance may have important implications in the development of strategies for overcoming cancer cell resistance to chemotherapy.
耐药性是癌症治疗的主要障碍。我们之前的研究表明,miR-125b 在耐药性中发挥重要作用。在这里,我们报告了一种新的机制,即通过 Snail 激活的 Wnt/β-catenin/TCF4 轴上调 miR-125b,从而增加癌症干细胞的数量。Snail 通过上调 miR-125b 来抑制 Bak1,从而赋予肿瘤细胞耐药性。通过恢复 Bak1 的表达或耗尽 miR-125b,可以使表达 Snail 的癌细胞重新对紫杉醇敏感,这表明 miR-125b 在 Snail 诱导的耐药性中起关键作用。此外,过表达 miR-125b 可显著增加癌症干细胞群体(CD24-CD44+),而耗尽 miR-125b 或恢复 Bak1 的表达可增加 Snail 过表达细胞中的非干细胞群体(CD24+CD44+)。这些发现有力地支持了 miR-125b 作为 Snail 诱导的癌症干细胞富集和耐药性的关键介质的作用。这种 Snail 诱导的干细胞增殖和耐药性的新机制可能对开发克服癌细胞对化疗耐药性的策略具有重要意义。