期刊
CANCER LETTERS
卷 402, 期 -, 页码 190-202出版社
ELSEVIER IRELAND LTD
DOI: 10.1016/j.canlet.2017.06.002
关键词
Non-small cell lung cancer (NSCLC); Epithelial-mesenchymal transition (EMT); Slug; miR-137; TFAP2C
类别
资金
- National Taiwan University [103R7601-3]
- Far Eastern Memorial Hospital-National Taiwan University Hospital Joint Research Program [105-FTN02]
The epithelial-mesenchymal transition (EMT) regulator, Slug, plays multifaceted roles in controlling lung cancer progression, but its downstream targets and mechanisms in promoting lung cancer progression have not been well defined. In particular, the miRNAs downstream of Slug in non-small cell lung cancer (NSCLC) remain undetermined. Here, we report that miR-137 is downstream of the EMT regulator, Slug, in lung cancer cells. Slug binds directly to the E-box of the miR-137 promoter and up-regulates its expression in lung cancer cells. Knockdown of miR-137 abolished Slug-induced cancer invasion and migration, whereas upregulation of miR-137 was found to trigger lung cancer cell invasion and progression by direct suppressing TFAP2C (transcription factor AP-2 gamma). Clinical data showed that lung adenocarcinoma patients with low-level expression of Slug and miR-137 but high-level expression of TFAP2C experienced significantly better survival. miR-137 is a Slug-induced miRNA that relays the pro metastatic effects of Slug by targeting TFAP2C. Our findings add new components to the Slug-mediated regulatory network in lung cancer, and suggest that Slug, miR-137, and TFAP2C may be useful prognostic markers in lung adenocarcinoma. (C) 2017 Elsevier B.V. All rights reserved.
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