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微小RNA-10a在非小细胞肺癌中上调,可能通过靶向磷酸酶和张力蛋白同源物(PTEN)来促进癌症发展。

MiRNA-10a is upregulated in NSCLC and may promote cancer by targeting PTEN.

作者信息

Yu Tao, Liu Lei, Li Jing, Yan Mingxia, Lin Hechun, Liu Ying, Chu Dandan, Tu Hong, Gu Aiqin, Yao Ming

机构信息

State Key Laboratory of Oncogenes and Related Genes, Shanghai Cancer Institute, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Oncotarget. 2015 Oct 6;6(30):30239-50. doi: 10.18632/oncotarget.4972.

Abstract

MicroRNAs (miRNAs) are involved in human cancer including non-small cell lung cancer (NSCLC). In this study, we compared miRNA expression microarray of SPC-A-1sci (high metastatic) and SPC-A-1 (weakly metastatic) cells. We found that miRNA-10a was up-regulated in NSCLC compared with corresponding normal tissues. High expression of miR-10a was associated with tumor node metastasis and lymph node metastasis. Furthermore, overexpression of miR-10a promoted NSCLC cell proliferation, migration and invasion in vitro. We found that PTEN was a direct target of miR-10a in NSCLC. Also miR-10a activated the PTEN/AKT/ERK pathway. We suggest that miR-10a contributes to NSCLC by targeting PTEN.

摘要

微小RNA(miRNA)参与包括非小细胞肺癌(NSCLC)在内的人类癌症。在本研究中,我们比较了SPC-A-1sci(高转移性)和SPC-A-1(低转移性)细胞的miRNA表达微阵列。我们发现,与相应的正常组织相比,NSCLC中miRNA-10a上调。miR-10a的高表达与肿瘤结节转移和淋巴结转移相关。此外,miR-10a的过表达促进了NSCLC细胞在体外的增殖、迁移和侵袭。我们发现PTEN是NSCLC中miR-10a的直接靶点。并且miR-10a激活了PTEN/AKT/ERK通路。我们认为miR-10a通过靶向PTEN促进NSCLC的发生发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ebdc/4745794/f562a1e4664d/oncotarget-06-30239-g001.jpg

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