| Literature DB >> 27836543 |
Changshan Song1, Pingfang Lu2, Guoqiang Sun2, Lin Yang3, Zhigang Wang4, Zheng Wang5.
Abstract
Cisplatin is the most potent and widespread used chemotherapy drug for lung cancer treatment. However, a large proportion of NSCLC patients were insensitive to chemotherapy. This study explored the role of miR-34a in regulating sensitivity of NSCLC cells to cisplatin and its downstream targets. The quantitative PCR result showed that miR-34a expression was upregulated in cisplatin sensitive NSCLC patients compared cisplatin insensitive NSCLC controls. By applying loss-and-gain function analysis, we demonstrated that miR-34a directly targeted to MYCN to sensitize NSCLC cells to cisplatin. In addition, p53 was found to monitor the expression of miR-34a in NSCLC cells after cisplatin treatment. Therefore, the sensitivity of cisplatin in NSCLC cells was modulated via p53/miR-34a/MYCN axis.Entities:
Keywords: Cisplatin; MYCN; NSCLC; miR-34a; p53
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Year: 2016 PMID: 27836543 DOI: 10.1016/j.bbrc.2016.11.037
Source DB: PubMed Journal: Biochem Biophys Res Commun ISSN: 0006-291X Impact factor: 3.575