Suppr超能文献

HOMER3通过上调EZH2并介导miR-361/GPNMB轴促进肝细胞癌进展。

HOMER3 promotes liver hepatocellular carcinoma cancer progression by -upregulating EZH2 and mediating miR-361/GPNMB axis.

作者信息

Chen Lixia, Shan Xiangxiang, Wan Xinqiang, Zha Wenzhang, Fan Rengen

机构信息

Medical College of Nantong University, China.

Department of Geriatric Medicine, the Forth Affiliated Hospital of Nantong University, the First People's Hospital of Yancheng, China.

出版信息

Pathol Res Pract. 2024 Feb;254:155150. doi: 10.1016/j.prp.2024.155150. Epub 2024 Jan 19.

Abstract

Liver hepatocellular carcinoma (LIHC) is among the most lethal human cancers. Studies have shown that Homer scaffold protein 3 (HOMER3) plays important roles in various diseases and cancers, but its biological function and molecular mechanism in LIHC have never been investigated. Our study discovered the aberrantly high expression of HOMER3 and its promising diagnostic and prognostic significance in LIHC. Functionally, HOMER3 knockdown inhibited the proliferative and migrative abilities of LIHC cells and tumor growth in vivo. Mechanically, HOMER3 mediated the aggressiveness of LIHC cells via GPNMB. Meanwhile, miR-361 directly targeted GPNMB and attenuated LIHC progression by suppressing GPNMB expression. The regulatory effect of HOMER3 during LIHC progression was exerted through the miR-361/GPNMB axis. Furthermore, EZH2 supplementation or miR-361 depletion effectively abated the tumor-suppressive effect of HOMER3 knockdown on LIHC progression. In conclusion, HOMER3 mediated LIHC progression through the EZH2/miR-361/GPNMB axis.

摘要

肝细胞癌(LIHC)是最致命的人类癌症之一。研究表明,Homer支架蛋白3(HOMER3)在各种疾病和癌症中发挥重要作用,但其在LIHC中的生物学功能和分子机制尚未得到研究。我们的研究发现了HOMER3在LIHC中异常高表达及其在诊断和预后方面的重要意义。在功能上,敲低HOMER3可抑制LIHC细胞的增殖和迁移能力以及体内肿瘤生长。在机制上,HOMER3通过GPNMB介导LIHC细胞的侵袭性。同时,miR-361直接靶向GPNMB并通过抑制GPNMB表达减弱LIHC进展。HOMER3在LIHC进展过程中的调节作用是通过miR-361/GPNMB轴发挥的。此外,补充EZH2或耗尽miR-361可有效减轻敲低HOMER3对LIHC进展的肿瘤抑制作用。总之,HOMER3通过EZH2/miR-361/GPNMB轴介导LIHC进展。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验