Department of Medical Oncology, VU University Medical Center, Amsterdam, The Netherlands.
Crit Rev Oncol Hematol. 2012 Feb;81(2):103-22. doi: 10.1016/j.critrevonc.2011.03.010. Epub 2011 May 5.
Drug resistance remains a major problem in the treatment of cancer patients for both conventional chemotherapeutic and novel biological agents. Intrinsic or acquired resistance can be caused by a range of mechanisms, including increased drug elimination, decreased drug uptake, drug inactivation and alterations of drug targets. Recent data showed that other than by genetic (mutation, amplification) and epigenetic (DNA hypermethylation, histone post-translational modification) changes, drug resistance mechanisms might also be regulated by microRNAs (miRNAs). In this review we provide an overview on the role of miRNAs in anticancer drug resistance, reporting the main studies on alterations in cell survival and/or apoptosis pathways, as well as in drug targets and determinants of drug metabolism, mediated by deregulation of miRNA expression. The current status of pharmacogenetic studies on miRNA and their possible role in cancer stem cell drug resistance are also discussed. Finally, we integrated the preclinical data with clinical evidences, in lung and pancreatic cancers, showing how the study of miRNAs could help to predict resistance of individual tumours to different anticancer drugs, and guide the oncologists in the selection of rationally based tailor-made treatments.
耐药性仍然是癌症患者治疗中面临的主要问题,无论是传统的化疗药物还是新型的生物制剂。内在或获得性耐药性可能由多种机制引起,包括药物清除增加、药物摄取减少、药物失活和药物靶点改变。最近的数据表明,除了遗传(突变、扩增)和表观遗传(DNA 超甲基化、组蛋白翻译后修饰)变化外,耐药机制也可能受到 microRNAs(miRNAs)的调节。在这篇综述中,我们概述了 miRNAs 在抗癌药物耐药性中的作用,报告了主要关于细胞存活和/或细胞凋亡途径改变的研究,以及药物靶点和药物代谢决定因素的改变,这些改变是由 miRNA 表达失调介导的。还讨论了 miRNA 的遗传药理学研究的现状及其在癌症干细胞耐药性中的可能作用。最后,我们将临床前数据与临床证据整合在一起,以肺癌和胰腺癌为例,说明了 miRNA 的研究如何有助于预测个体肿瘤对不同抗癌药物的耐药性,并指导肿瘤学家合理选择基于个体化的定制治疗。