CHEN Hui, JIANG Miao, XIN Li-li, et al. Effect of Drug-containing Serum with Modified Shengmai Decoction on Proliferation and Migration of Non Small Cell Lung Carcinoma Cells[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(19): 106-110.
CHEN Hui, JIANG Miao, XIN Li-li, et al. Effect of Drug-containing Serum with Modified Shengmai Decoction on Proliferation and Migration of Non Small Cell Lung Carcinoma Cells[J]. Chinese journal of experimental traditional medical formulae, 2015, 21(19): 106-110. DOI: 10.13422/j.cnki.syfjx.2015190106.
Western blot法检测E钙连蛋白(E-cad)及波形蛋白(Vimentin)蛋白表达的变化。结果:与空白血清组相比
加味生脉饮含药血清作用H460细胞24 h后
细胞增殖抑制率上升(P<0.01)
S期细胞百分率增高(P<0.01)
划痕距离较长
E-cad蛋白含量升高(P<0.01)
Vimentin蛋白含量降低(P<0.01)。结论:加味生脉饮对H460细胞增殖有一定抑制作用
主要途径为S期阻滞。加味生脉饮可以抑制H460细胞的转移
其机制可能与干预H460细胞上皮间质转化有关。
Abstract
Objective: To study the effect of drug-containing serum with modified Shengmai decoction on cell proliferation
cell cycle and migration of non small cell lung carcinoma(NSCLC)H460 cells
and investigate its molecular mechanisms. Method: Drug-containing serum with modified Shengmai decoction was prepared by administering the rabbits with 18 g·kg-1 crude drug ig
and blank control serum was prepared with the same volume of normal saline(NS) ig. Both serum was regarded as a concentration of 100%. H460 cells were cultured in vitro and cells in logarithmic growth phase were collected. 10% control serum group
2.5%
5%
10% drug-containing serum groups and 1 mg·L-1 DDP group were established. Cell density was adjusted to 3 000 cells/mL. After serum action for 24
48 hours
four methyl azo blue(MTT) method was used to measure the proliferation inhibition rate. Cell density was then adjusted to 5×105 cells/mL
and after serum action for 24 hours
flow cytometry was used to test cell cycle
scratch assay was taken to observe cell migration
and Western blot method was used to measure the expression changes of E-cadherin(E-cad) and Vimentin. Result: Compared with the blank control group
drug-containing serum with modified Shengmai decoction had higher cell proliferation inhibition rate (P<0.01)
higher cells percentage in S phase(P<0.01)
longer wound scratch distance
higher protein content of E-cad and lower Vimentin (P<0.01) after serum action for 24 hours. Conclusion: Modified Shengmai decoction has an inhibition effect on cell H460 mainly by inhibiting cells in phase S. Modified Shengmai decoction can inhibit the metastasis of H460
whose mechanism may be associated with intervening the epithelial-mesenchymal transformation.