Sun Jing-Xia, Meng Zhuo-Xian, Lv Jing-Huan, Sun Yu-Jie
Key Laboratory of Human Functional Genomics of Jiangsu Province, Nanjing Medical University, Nanjing 210029, P. R. China.
Ai Zheng. 2006 Aug;25(8):960-6.
BACKGROUND & OBJECTIVE: Peroxisome proliferator-activated receptor gamma (PPARgamma) is known to be highly expressed in breast cancer tissues. Thiazolidinediones (TZD), the specific ligands for PPARgamma, can inhibit cell proliferation and induce apoptosis. This study was to investigate the possibility of using troglitazone, one of TZD, as the sensitizer of epirubicin in the treatment of estrogen receptor (ER) negative breast cancer.
MTT assay and flow cytometry were used to examine the cell proliferation and apoptosis in two ER negative breast cancer cell line MDA-MB-435S and MDA-MB-231. Cells were treated with either troglitazone or epirubicin alone or co-treated with troglitazone and epirubicin. Western blot analysis was used to assess the expression level of Bcl-2. The migration potential of cells with different treatments was analyzed by the wound healing assay.
The effect of epirubicin on inhibiting cell proliferation of breast cancer cells was enhanced by co-treatment with troglitazone in the range of 4 micromol/L to 24 micromol/L. The 50% inhibitory concentration (IC(50)) of epirubicin was reduced to 60% when combined with troglitazone compared to the treatment with epirubicin only. Treatment of cells with troglitazone or epirubicin alone could not induce significant apoptosis. However, the apoptotic indexes of MDA-MB-435S and MDA-MB-231 cells co-treated with troglitazone and epirubicin were (5.48+/-0.45)% and (10.08+/-1.89)%, respectively. Co-treatment with troglitazone and epirubicin further downregulated the expression level of Bcl-2 and inhibited cell migration simultaneously.
Troglitazone could not only augment the effect of epirubicin on inhibiting cell proliferation and inducing apoptosis, but also suppress the migration of breast cancer cells. Troglitazone may sensitize the effect of epirubicin on breast cancer cells.
已知过氧化物酶体增殖物激活受体γ(PPARγ)在乳腺癌组织中高表达。噻唑烷二酮类(TZD)是PPARγ的特异性配体,可抑制细胞增殖并诱导凋亡。本研究旨在探讨使用TZD之一的曲格列酮作为表柔比星治疗雌激素受体(ER)阴性乳腺癌的增敏剂的可能性。
采用MTT法和流式细胞术检测两株ER阴性乳腺癌细胞系MDA-MB-435S和MDA-MB-231的细胞增殖和凋亡情况。细胞分别单独用曲格列酮或表柔比星处理,或同时用曲格列酮和表柔比星处理。采用蛋白质印迹分析评估Bcl-2的表达水平。通过伤口愈合试验分析不同处理细胞的迁移潜能。
在4μmol/L至24μmol/L范围内,曲格列酮与表柔比星联合处理增强了表柔比星对乳腺癌细胞增殖的抑制作用。与仅用表柔比星处理相比,曲格列酮联合表柔比星时表柔比星的50%抑制浓度(IC50)降低至60%。单独用曲格列酮或表柔比星处理细胞均不能诱导明显凋亡。然而,曲格列酮和表柔比星联合处理的MDA-MB-435S和MDA-MB-231细胞的凋亡指数分别为(5.48±0.45)%和(10.08±1.89)%。曲格列酮和表柔比星联合处理进一步下调了Bcl-2的表达水平并同时抑制细胞迁移。
曲格列酮不仅可增强表柔比星对细胞增殖的抑制和凋亡诱导作用,还可抑制乳腺癌细胞的迁移。曲格列酮可能使表柔比星对乳腺癌细胞的作用增敏。