Journal
FEBS LETTERS
Volume 587, Issue 18, Pages 3069-3075Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.febslet.2013.06.058
Keywords
Gastric cancer; Multidrug resistance; miR-106a; Runt-related transcription factor 3
Ask authors/readers for more resources
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. (C) 2013 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available