Department of Chemical Biology and Therapeutics, St Jude Children's Research Hospital, Memphis, TN, USA.
School of Biosciences, University of Kent, Canterbury, UK.
Oncogene. 2014 Jul 10;33(28):3717-29. doi: 10.1038/onc.2013.330. Epub 2013 Aug 12.
Chemotherapy is the most common treatment for cancer. However, multidrug resistance (MDR) remains a major obstacle to effective chemotherapy, limiting the efficacy of both conventional chemotherapeutic and novel biologic agents. The constitutive androstane receptor (CAR), a xenosensor, is a key regulator of MDR. It functions in xenobiotic detoxification by regulating the expression of phase I drug-metabolizing enzymes and ATP-binding cassette (ABC) transporters, whose overexpression in cancers and whose role in drug resistance make them potential therapeutic targets for reducing MDR. MicroRNAs (miRNAs) are endogenous negative regulators of gene expression and have been implicated in most cellular processes, including drug resistance. Here, we report the inversely related expression of miR-137 and CAR in parental and doxorubicin-resistant neuroblastoma cells, wherein miR-137 is downregulated in resistant cells. miR-137 overexpression resulted in downregulation of CAR protein and mRNA (via mRNA degradation); it sensitized doxorubicin-resistant cells to doxorubicin (as shown by reduced proliferation, increased apoptosis and increased G2-phase cell cycle arrest) and reduced the in vivo growth rate of neuroblastoma xenografts. We observed similar results in cellular models of hepatocellular and colon cancers, indicating that the doxorubicin-sensitizing effect of miR-137 is not tumor type-specific. Finally, we show for the first time a negative feedback loop whereby miR-137 downregulates CAR expression and CAR downregulates miR-137 expression. Hypermethylation of the miR-137 promoter and negative regulation of miR-137 by CAR contribute in part to reduced miR-137 expression and increased CAR and MDR1 expression in doxorubicin-resistant neuroblastoma cells. These findings demonstrate that miR-137 is a crucial regulator of cancer response to doxorubicin treatment, and they identify miR-137 as a highly promising target to reduce CAR-driven doxorubicin resistance.
化疗是癌症最常见的治疗方法。然而,多药耐药性(MDR)仍然是有效化疗的主要障碍,限制了传统化疗药物和新型生物制剂的疗效。组成型雄烷受体(CAR)是一种外源性传感器,是 MDR 的关键调节因子。它通过调节 I 期药物代谢酶和 ABC 转运蛋白的表达来发挥作用,这些蛋白在癌症中的过度表达及其在耐药性中的作用使它们成为降低 MDR 的潜在治疗靶点。microRNAs(miRNAs)是基因表达的内源性负调节剂,参与了大多数细胞过程,包括耐药性。在这里,我们报告了亲本和多柔比星耐药神经母细胞瘤细胞中 miR-137 和 CAR 的表达呈负相关,其中 miR-137 在耐药细胞中下调。miR-137 的过表达导致 CAR 蛋白和 mRNA 的下调(通过 mRNA 降解);它使多柔比星耐药细胞对多柔比星敏感(表现为增殖减少、凋亡增加和 G2 期细胞周期阻滞增加),并降低神经母细胞瘤异种移植物的体内生长速度。我们在肝癌和结肠癌的细胞模型中观察到类似的结果,表明 miR-137 的多柔比星增敏作用不是肿瘤类型特异性的。最后,我们首次观察到负反馈环,即 miR-137 下调 CAR 表达,CAR 下调 miR-137 表达。miR-137 启动子的高甲基化和 CAR 对 miR-137 的负调控部分导致 miR-137 表达减少,多柔比星耐药神经母细胞瘤中 CAR 和 MDR1 表达增加。这些发现表明 miR-137 是癌症对多柔比星治疗反应的关键调节因子,并将 miR-137 鉴定为降低 CAR 驱动的多柔比星耐药性的极具前景的靶点。