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miRNA-145 通过靶向 OCT4 抑制肺腺癌细胞起始细胞的增殖。

microRNA-145 suppresses lung adenocarcinoma-initiating cell proliferation by targeting OCT4.

机构信息

Department of Thoracic Surgery, Nanjing Medical University Affiliated Cancer Hospital of Jiangsu Province, Cancer Institution of Jiangsu Province, Nanjing 210009, PR China.

出版信息

Oncol Rep. 2011 Jun;25(6):1747-54. doi: 10.3892/or.2011.1252. Epub 2011 Apr 7.

Abstract

Recent studies demonstrated that microRNA-145 is downregulated in human cancer cells and may function as a tumor suppressor. However, its role in lung cancer tumorigenesis remains unclear. Here, we demonstrated that upregulation of miR-145 reduced the proliferation and invasion as well as the ratio of CD133-positive initiating cells and the tumorosphere growth capacity of the human lung adenocarcinoma A549 cell line. The direct targeting of miR-145 to OCT4 mRNA was predicted by bioinformatic analysis and validated by a luciferase reporter system. We, therefore, confirmed that miR-145 can impair the proliferation of human lung adenocarcinoma-initiating cells by targeting OCT4 and leads to inhibition of lung cancer development.

摘要

最近的研究表明,miR-145 在人类癌细胞中下调,可能作为肿瘤抑制因子发挥作用。然而,其在肺癌肿瘤发生中的作用尚不清楚。在这里,我们证明 miR-145 的上调降低了人肺腺癌细胞系 A549 的增殖和侵袭能力,以及 CD133 阳性起始细胞的比例和肿瘤球生长能力。生物信息学分析预测 miR-145 可直接靶向 OCT4 mRNA,并通过荧光素酶报告系统得到验证。因此,我们证实 miR-145 可以通过靶向 OCT4 损害人肺腺癌细胞起始细胞的增殖,从而抑制肺癌的发展。

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