Suppr超能文献

微小RNA-216a可能通过靶向Janus激酶2来抑制胰腺肿瘤生长。

miR-216a may inhibit pancreatic tumor growth by targeting JAK2.

作者信息

Hou Bao-hua, Jian Zhi-xiang, Cui Peng, Li Shao-jie, Tian Rui-qing, Ou Jin-rui

机构信息

Department of General Surgery, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, PR China.

Department of General Surgery, Guangdong General Hospital, Guangdong Academy of Medical Sciences, Guangzhou 510080, PR China.

出版信息

FEBS Lett. 2015 Aug 4;589(17):2224-32. doi: 10.1016/j.febslet.2015.06.036. Epub 2015 Jul 3.

Abstract

This study was aimed to investigate miR-216a expression in pancreatic cancer and determine its effects on proliferation. miR-216a was found downregulated in pancreatic cancer tissues as compared to benign pancreatic lesions. JAK2 was identified as a miR-216a gene target. Further, in vivo treatment of PANC-1 tumors with miR-216a reduced JAK2 protein levels in the tumor and reduced tumor volume. In conclusion, miR-216a may function as a tumor suppressor regulating pancreatic cancer cells by targeting the JAK/STAT pathway. Further studies with a larger number of patient samples are necessary to fully explore the diagnostic and therapeutic potential of miR-216a for pancreatic cancer.

摘要

本研究旨在调查miR-216a在胰腺癌中的表达,并确定其对增殖的影响。与良性胰腺病变相比,发现miR-216a在胰腺癌组织中表达下调。JAK2被确定为miR-216a的基因靶点。此外,用miR-216a对PANC-1肿瘤进行体内治疗可降低肿瘤中JAK2蛋白水平并减小肿瘤体积。总之,miR-216a可能作为一种肿瘤抑制因子,通过靶向JAK/STAT途径调节胰腺癌细胞。需要对更多患者样本进行进一步研究,以充分探索miR-216a在胰腺癌诊断和治疗方面的潜力。

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