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微小RNA-141靶向锌指E盒结合蛋白2以抑制肝癌进展。

MiR-141 targets ZEB2 to suppress HCC progression.

作者信息

Wu Shi-Min, Ai Hong-Wu, Zhang Ding-Yu, Han Xiao-Qun, Pan Qin, Luo Feng-Ling, Zhang Xiao-Lian

机构信息

State Key Laboratory of Virology, Department of Immunology, Hubei Province Key Laboratory of Allergy and Immunology, School of Basic Medical Sciences, Wuhan University, Donghu Road 185#, Wuhan, 430071, Hubei Province, China.

出版信息

Tumour Biol. 2014 Oct;35(10):9993-7. doi: 10.1007/s13277-014-2299-9. Epub 2014 Jul 10.

Abstract

Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related deaths worldwide. Increasing evidence suggests that microRNAs (miRNAs) are associated with HCC tumorigenesis. The present study was designed to define the role of miR-141 in HCC. The expression of miR-141 was significantly decreased in four HCC cell lines. Overexpression of miR-141 suppressed both the growth and the motility of HCC cells. Furthermore, we identified zinc finger E-box binding homeobox 2 (ZEB2) as a target of miR-141 and miR-141 functioned as a tumor suppressor via ZEB2 targeting in HCC. These data provide a novel potential therapeutic target for HCC treatment.

摘要

肝细胞癌(HCC)是全球癌症相关死亡的主要原因之一。越来越多的证据表明,微小RNA(miRNA)与HCC的肿瘤发生有关。本研究旨在确定miR-141在HCC中的作用。miR-141在四种HCC细胞系中的表达显著降低。miR-141的过表达抑制了HCC细胞的生长和运动能力。此外,我们确定锌指E盒结合同源框2(ZEB2)为miR-141的一个靶点,并且miR-141在HCC中通过靶向ZEB2发挥肿瘤抑制作用。这些数据为HCC治疗提供了一个新的潜在治疗靶点。

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