Copyright
©The Author(s) 2017.
World J Gastroenterol. Mar 14, 2017; 23(10): 1816-1827
Published online Mar 14, 2017. doi: 10.3748/wjg.v23.i10.1816
Published online Mar 14, 2017. doi: 10.3748/wjg.v23.i10.1816
Figure 5 miR-34a inhibited oxaliplatin-induced autophagy in colorectal cancer cells.
A: HT29 and HT29-oxaliplatin (OXA) cells were transfected with miR-34a mimics and treated with or without OXA (10 μmol/L) simultaneously. After 48 h, autophagy was determined using a fluorescent dye (monodansylcadaverine, MDC) and flow cytometry; B: The above cell lysates were examined with indicated antibodies by western blotting. β-actin was used as loading control. (eP < 0.001 indicates a significant difference vs normal control; cP < 0.05 indicates a significant difference vs transfection with miR-34a mimic group).
- Citation: Sun C, Wang FJ, Zhang HG, Xu XZ, Jia RC, Yao L, Qiao PF. miR-34a mediates oxaliplatin resistance of colorectal cancer cells by inhibiting macroautophagy via transforming growth factor-β/Smad4 pathway. World J Gastroenterol 2017; 23(10): 1816-1827
- URL: https://www.wjgnet.com/1007-9327/full/v23/i10/1816.htm
- DOI: https://dx.doi.org/10.3748/wjg.v23.i10.1816