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Targeting of miR34a-NOTCH1 axis reduced breast cancer stemness and chemoresistance.靶向 miR34a-NOTCH1 轴降低乳腺癌干细胞特性和化疗耐药性。
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MicroRNA-191, by promoting the EMT and increasing CSC-like properties, is involved in neoplastic and metastatic properties of transformed human bronchial epithelial cells.微小RNA-191通过促进上皮-间质转化并增强肿瘤干细胞样特性,参与转化的人支气管上皮细胞的肿瘤形成和转移特性。
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MicroRNA-29b-1 impairs in vitro cell proliferation, self‑renewal and chemoresistance of human osteosarcoma 3AB-OS cancer stem cells.MicroRNA-29b-1 可损害人骨肉瘤 3AB-OS 肿瘤干细胞的体外细胞增殖、自我更新和化疗耐药性。
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MicroRNA-1246 expression associated with CCNG2-mediated chemoresistance and stemness in pancreatic cancer.微小RNA-1246的表达与CCNG2介导的胰腺癌化疗耐药性及干性相关。
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微小RNA在癌症干细胞中的新兴作用:对癌症治疗的影响。

Emerging role of microRNAs in cancer stem cells: Implications in cancer therapy.

作者信息

Garg Minal

机构信息

Minal Garg, Department of Biochemistry, University of Lucknow, Lucknow 226007, India.

出版信息

World J Stem Cells. 2015 Sep 26;7(8):1078-89. doi: 10.4252/wjsc.v7.i8.1078.

DOI:10.4252/wjsc.v7.i8.1078
PMID:26435768
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4591786/
Abstract

A small subset of cancer cells that act as tumor initiating cells or cancer stem cells (CSCs) maintain self-renewal and growth promoting capabilities of cancer and are responsible for drug/treatment resistance, tumor recurrence and metastasis. Due to their potential clinical importance, many researchers have put their efforts over decades to unravel the molecular mechanisms that regulate CSCs functions. MicroRNAs (miRNAs) which are 21-23 nucleotide long, endogenous non-coding RNAs, regulate gene expression through gene silencing at post-transcriptional level by binding to the 3'-untranslated regions or the open reading frames of target genes, thereby result in target mRNA degradation or its translational repression and serve important role in several cellular, physiological and developmental processes. Aberrant miRNAs expression and their implication in CSCs regulation by controlling asymmetric cell division, drug/treatment resistance and metastasis make miRNAs a tool of great therapeutic potential against cancer. Recent advancements on the biological complexities of CSCs, modulation in CSCs properties by miRNA network and development of miRNA based treatment strategies specifically targeting the CSCs as an attractive therapeutic targets for clinical application are being critically analysed.

摘要

一小部分作为肿瘤起始细胞或癌症干细胞(CSCs)的癌细胞维持着癌症的自我更新和生长促进能力,并导致耐药性/治疗抵抗、肿瘤复发和转移。由于其潜在的临床重要性,几十年来许多研究人员致力于揭示调节CSCs功能的分子机制。微小RNA(miRNAs)是长度为21 - 23个核苷酸的内源性非编码RNA,通过在转录后水平与靶基因的3'非翻译区或开放阅读框结合来沉默基因表达,从而导致靶mRNA降解或其翻译抑制,并在多个细胞、生理和发育过程中发挥重要作用。异常的miRNAs表达及其通过控制不对称细胞分裂、耐药性/治疗抵抗和转移在CSCs调节中的作用,使miRNAs成为一种具有巨大癌症治疗潜力的工具。本文对CSCs生物学复杂性、miRNA网络对CSCs特性的调节以及基于miRNA的治疗策略的发展等方面的最新进展进行了批判性分析,这些治疗策略将CSCs作为临床应用中极具吸引力的治疗靶点。