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微小RNA-493抑制胰腺癌细胞的增殖和侵袭,并反向调节人醚-去极化激活的钾离子通道1(hERG1)的表达。

miR-493 inhibits proliferation and invasion in pancreatic cancer cells and inversely regulated hERG1 expression.

作者信息

Zhi Duo, Zhao Xin, Dong Mei, Yan Caichuan

机构信息

Department of Pharmacy, Harbin Medical University Cancer Hospital, Harbin, Heilongjiang 150040, P.R. China.

Department of Pharmacology, College of Pharmacy, Harbin Medical University, Harbin, Heilongjiang 150081, P.R. China.

出版信息

Oncol Lett. 2017 Dec;14(6):7398-7404. doi: 10.3892/ol.2017.7178. Epub 2017 Oct 12.

Abstract

The human ether-a-go-go-related potassium channel 1 (hERG1) is a component of the voltage-gated Kv11.1 potassium channel, which has been recently indicated to have a crucial role in the tumorigenesis of multiple tumors, including pancreatic carcinoma. Pancreatic carcinoma is one of the most malignant human cancer types, which has an extremely poor prognosis. The present study demonstrated that the expression levels of hERG1 were markedly elevated in pancreatic cancer tissues and pancreatic cancer cell lines, and that the abnormal hERG1 expression was significantly associated with the proliferation and invasion ability of pancreatic cancer. Furthermore, hERG1 was identified to be a direct target of miR-493, which is generally reduced in pancreatic cancer tissues and cell lines. These findings provide a novel insight into the regulatory mechanism of miR-493/hERG1 in pancreatic cancer cell proliferation and invasion, which may aid the development of novel diagnostic and therapeutic strategies for pancreatic cancer in the future.

摘要

人类醚-去极化相关钾通道1(hERG1)是电压门控Kv11.1钾通道的一个组成部分,最近研究表明其在包括胰腺癌在内的多种肿瘤的发生过程中起关键作用。胰腺癌是人类最恶性的癌症类型之一,预后极差。本研究表明,hERG1在胰腺癌组织和胰腺癌细胞系中的表达水平显著升高,且hERG1的异常表达与胰腺癌的增殖和侵袭能力显著相关。此外,hERG1被确定为miR-493的直接靶点,而miR-493在胰腺癌组织和细胞系中通常表达降低。这些发现为miR-493/hERG1在胰腺癌细胞增殖和侵袭中的调控机制提供了新的见解,可能有助于未来开发针对胰腺癌的新型诊断和治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b8fe/5755206/e3f57bc7b501/ol-14-06-7398-g00.jpg

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