| Literature DB >> 23932924 |
Yi Zhang1, Qiping Lu, Xun Cai.
Abstract
Multidrug resistance (MDR) is the main barrier to the success of chemotherapy for gastric cancer (GC). miR-106a, which is highly expressed in GC, influences a variety of aspects of GC. However, the function of miR-106a in MDR of GC still remains unclear. In the present study, we found that miR-106a is elevated in MDR cell lines. miR-106a promotes chemo-resistance of GC cells, accelerates ADR efflux, and suppresses drug-induced apoptosis. Finally, we show that runt-related trans factor 3 (RUNX3) is the functional target of miR-106a. Collectively, these findings demonstrate that miR-106a may promote MDR in GC cells by targeting RUNX3.Entities:
Keywords: Gastric cancer; Multidrug resistance; Runt-related transcription factor 3; miR-106a
Mesh:
Substances:
Year: 2013 PMID: 23932924 DOI: 10.1016/j.febslet.2013.06.058
Source DB: PubMed Journal: FEBS Lett ISSN: 0014-5793 Impact factor: 4.124