Copyright
©The Author(s) 2015.
World J Gastroenterol. Aug 21, 2015; 21(31): 9348-9357
Published online Aug 21, 2015. doi: 10.3748/wjg.v21.i31.9348
Published online Aug 21, 2015. doi: 10.3748/wjg.v21.i31.9348
Figure 3 Effect of linc00675 knockdown on pancreatic ductal adenocarcinoma growth in vitro.
A: Knockout efficiency of siRNA targeting Linc00675 was confirmed by quantitative real time-polymerase chain reaction in SW1990 and MIA PaCa-2 cell lines, cP < 0.001, NC vs siLINC00675, Student’s t-test; B: Effects of knockdown of linc00675 on the proliferation of SW1990 and MIA PaCa-2 cells were assessed with MTT assay; C: Cell cycle of SW1990 and MIA PaCa-2 was analyzed by flow cytometry 48 h after transfection; D: Effect of knockdown of linc00675 on percentage of cells in G1-G0, S, and G2-M phase was examined quantitatively, aP < 0.05, NC vs siLINC00675, Student’s t-test; E: Cells were untreated, or transfected with linc00675, then the expression of CyclinA, CDK2, CyclinE and CyclinD1 was detected by Western blot. Data are represented as the mean ± SD from three independent experiments.
- Citation: Li DD, Fu ZQ, Lin Q, Zhou Y, Zhou QB, Li ZH, Tan LP, Chen RF, Liu YM. Linc00675 is a novel marker of short survival and recurrence in patients with pancreatic ductal adenocarcinoma. World J Gastroenterol 2015; 21(31): 9348-9357
- URL: https://www.wjgnet.com/1007-9327/full/v21/i31/9348.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i31.9348