miRNA靶向RAS-MAPK通路的表观遗传性激活与肿瘤
作者: |
1丁苗,
2涂萍
1 江西中医药大学2014级中西医结合临床专业研究生,南昌 330004 2 南昌市第三医院内分泌代谢科,南昌 330009 |
通讯: |
涂萍
Email: tuping8877@126.com |
DOI: | 10.3978/j.issn.2095-6959.2016.11.034 |
基金: | 国家自然科学基金, 81260133 上海市糖尿病重点实验室开放课题资助项目, SHKLD-KF-1302 |
摘要
肿瘤作为一种难治性疾病,全世界都在为其治疗寻找新靶点。高度保守的RAS-MAPK通路在生物界大多数细胞内都广泛存在,主要通过各种级联反应刺激来控制细胞增殖分化等功能。体细胞基因突变编码RAS-MAPK通路经常发生在许多肿瘤中。miRNAs作为近年来研究较多的一种基因表达调控方式,其是通过与相关靶基因3’-UTR区结合来降解mRNA或抑制翻译表达。明确miRNA调控RAS-MAPK在肿瘤发生发展中的机制,可能为肿瘤的治疗提供新靶点。
关键词:
RAS-MAPK信号通路
miRNAs
肿瘤
Epigenetic activation the miRNAs target the RAS-MAPK pathway and cancer
CorrespondingAuthor: TU Ping Email: tuping8877@126.com
DOI: 10.3978/j.issn.2095-6959.2016.11.034
Abstract
As a refractory disease, people all over the world are looking for new targets for the treatment of tumor. The highly conserved RAS-MAPK pathway is involved in a wide range of cellular processes. It works with a variety of cascading reaction to control cell proliferation differentiation and other functions. Somatic genes mutations encoding the RAS-MAPK pathway often occur in many tumors. MicroRNAs are researched as a way of regulating the genic expression in recent years, and they degrade the mRNA or inhibit the translation by targeting the gene 3'-UTR region. Understanding the mechanism of how miRNA regulates the RAS-MAPK in the development of tumor may provide new targets for the treatment of tumor.