Chinese Clinical Oncology
• 论著 • Previous Articles Next Articles
MING Hao, ZONG Yun, XIE Quanqin, CHEN Lujun, XU Bin, LI Chong, JIANG Jingting.
Received:
Revised:
Online:
Published:
Contact:
Abstract:
Objective To investigate the inhibitory effects of toxoflavin on proliferation, apoptosis and migration of non-small cell lung cancer A549 cells. Methods The cultured A549 cells were treated with toxoflavin(0.5, 0.375, 0.25, 0.125 μmol/L) for 24 h and 48 h, the control group was treated with cell culture media only. CCK-8 assay was used to test the growth inhibitory rate and Annexin V/propidium iodide(PI)staining assay was applied to detect the apoptosis rate. The cell migration rate of 12 h, 24 h, 48 h were measured by the wound healing assay. Results The cell growth inhibition rates of A549 cells in experimental groups were (93.51±3.69)%,(40.38±3.08)%,(23.54±2.58)%,(13.07±2.37)% in 24 h and(90.53±3.58)%,(53.72±3.02)%,(34.44±3.10)%,(24.78±2.43)% in 48 h. The cell apoptosis rates of A549 cells in expremental groups were (78.68±2.22)%,(43.66±2.53)%,(20.81±2.59)%,(6.25±0.96)% in 24 h and(88.66±3.16)%, (59.86±2.81)%,(27.89±3.48)%,(9.91±1.33)% in 48 h, and those of control group were(1.57±0.52)% in 24 h and(1.59±0.55)% in 48 h respectively. The A549 cell migration rate of 12 h,24 h,48 h in experimental group(0.125 μmol/L) was 7%,11% and 16%,but it was 14%,26% and 39% in control group. Conclusion Toxoflavin could significantly inhibit proliferation and promote apoptosis of A549 cells in a dose and time dependent manner, and it could also weaken the migration capacity of A549 cells.
0 / / Recommend
Add to citation manager EndNote|Reference Manager|ProCite|BibTeX|RefWorks
URL: http://manu65.magtech.com.cn/Jwk3_lczlxzz/EN/
http://manu65.magtech.com.cn/Jwk3_lczlxzz/EN/Y2016/V21/I2/117
Cited