Literature DB >> 28454276

MicroRNA-134 reverses multidrug resistance in human lung adenocarcinoma cells by targeting FOXM1.

Jipeng Li1, Ying Chen1, Mingwei Jin1, Jianhua Wang1, Shanfeng Li1, Zhe Chen1, Wanjun Yu2.   

Abstract

Multidrug resistance (MDR) is the primary barrier to the success of chemotherapy for lung adenocarcinoma. MicroRNA (miR)-134, which is downregulated in lung adenocarcinoma, influences cell proliferation, apoptosis and invasion of lung adenocarcinoma. However, the function of miR-134 in the MDR of lung adenocarcinoma remains unclear. In the present study, it was identified that miR-134 expression is significantly downregulated in A549/cisplatin MDR lung adenocarcinoma cells, as compared with A549 parental cells. miR-134 regulates the sensitivity of lung adenocarcinoma cells to certain anticancer drugs. Furthermore, it was demonstrated that forkhead box M1 and multidrug resistance-associated protein 1 are functional targets of miR-134. These data revealed an important role for miR-134 in the regulation of MDR in lung adenocarcinoma.

Entities:  

Keywords:  forkhead box M1; lung adenocarcinoma; microRNA-134; multidrug resistance; multidrug resistance-associated protein 1

Year:  2017        PMID: 28454276      PMCID: PMC5403496          DOI: 10.3892/ol.2017.5574

Source DB:  PubMed          Journal:  Oncol Lett        ISSN: 1792-1074            Impact factor:   2.967


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