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微小 RNA-106a 通过靶向 TIMP2 调节胃癌的侵袭和转移。

MicroRNA-106a targets TIMP2 to regulate invasion and metastasis of gastric cancer.

机构信息

Department of Gastroenterology, First Affiliated Hospital of Xi'an Jiaotong University, 277 West Yanta Rood, Xi'an, Shanxi 710061, People's Republic of China.

Department of Pathology, General Hospital of Ningxia Medical University, Yinchuan, People's Republic of China.

出版信息

FEBS Lett. 2014 Feb 14;588(4):600-7. doi: 10.1016/j.febslet.2013.12.028. Epub 2014 Jan 17.

Abstract

Emerging evidence has shown that microRNA plays an important role in tumor development and progression. Here, we report that miR-106a is frequently up-regulated in gastric cancer tissues and positively correlates with metastasis. Restrained expression of miR-106a in gastric cancer cells significantly reduces their capacity of proliferation, migration and invasion. In tissue sections, the positive signal of miR-106a localized in metastasis-associated regions confirmed this result. Moreover, we show that TIMP2 is a direct downstream target for miR-106a and knockdown of TIMP2 strengthens the beneficial effects of miR-106a. Our study adds miR-106a to the complex mechanisms of tumor metastasis.

摘要

新出现的证据表明,microRNA 在肿瘤的发生和发展中起着重要作用。在这里,我们报告 miR-106a 在胃癌组织中经常上调,并与转移呈正相关。在胃癌细胞中抑制 miR-106a 的表达显著降低了它们的增殖、迁移和侵袭能力。在组织切片中,miR-106a 的阳性信号定位于转移相关区域,证实了这一结果。此外,我们还表明 TIMP2 是 miR-106a 的直接下游靶标,而 TIMP2 的敲低增强了 miR-106a 的有益作用。我们的研究将 miR-106a 添加到肿瘤转移的复杂机制中。

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