摘要
①目的探讨VP16对细胞凋亡的作用。②方法用两种剂量(3.12,6.25μmol)的VP16处理腹腔接种S-180瘤细胞和抗阿霉素瘤细胞(S-180-R)的BABL/C鼠。0,6,9h分别取腹水,用流式细胞仪测定细胞相对DNA含量。③结果VP16在3.12,6.25μmol剂量时,均可诱导S-180细胞凋亡,而剂量效应并不明显。在6.25μmol时,也可诱导S-180-R细胞凋亡,且VP16诱导S-180和S-180-R两种细胞凋亡差别不明显。④结论VP16是S-180和S-180-R细胞凋亡的诱导剂。VP16诱导的凋亡与其抗药表型关系不大,但与免疫机制似乎有一定的关系。
Objective To study the effect of VP16 on apoptosis. Methods BABL/C mice previously inoculated with parental S 180 and adriamycin resistant S 180 R cells were treated with two different dosages of VP16. S 180 and S 180 R cells drawn from the abdominal cavity at 0, 6, 9h and analyzed by flow cytometer FACS 420 for DNA content. Results VP16 could induce apoptosis in S 180 cells and the inducing effect of both dosages showed no significant difference. For S 180 R cells, only VP16 at dosage of 6.25μmol could induce apoptosis. The inducing effect of VP16 for both S 180 and S 180 R cells showed no significant difference. There was an increase of lymphocyte in the abdominal cavity along with the appearance of cell apoptosis. Conclusion VP16 is an apoptosis inducer for S 180 and S 180 R cells. Under present experiment condition, the apoptosis induced by VP16 is not closely correlated with the drug resistance phenotype of cells, but has certain relationship with the immune system.
出处
《青岛医学院学报》
1997年第3期193-194,共2页
Acta Academiae Medicinae Qingdao Universitatis
基金
山东省卫生厅资助
关键词
去甲鬼臼甙
肿瘤
抗药性
细胞凋亡
药物疗法
etoposide
apoptosis
cell transformation
neoplasm
drug resistance