Bilim V, Kawasaki T, Takahashi K, Tomita Y
Dept. of Urology. Niigata University School of Medicine, Japan.
J Exp Clin Cancer Res. 2000 Dec;19(4):483-8.
Adriamycin (ADM), widely used for systemic and local treatment of bladder tumors, triggers apoptosis in bladder cancer cells. Here we investigated the effect of ADM on cell cycle progression and expression of cell cycle regulating proteins in bladder cancer cell lines with various p53 and p21(WAF1/CIP1) status. Flowcytometric analysis was used to estimate the cell cycle distribution of T24, HT-1376, RT4, and SCaBER bladder cancer cell lines. Cell cycle regulating proteins were analyzed by Immunoblot. Treatment of RT4 cells, bearing wild type p53 and p21(WAF1/CIP1), with ADM induced expression of both proteins and cell cycle arrest, not in G1, as was anticipated, but in the G2 phase. Simultaneously, Retinoblastoma (Rb) protein expression was decreased. Expression of PCNA, which is a target gene of E2F, was not changed. The results suggest that even if the tumor cells bear wild type (wt) p53 and wt p21(WAF1/CIP1) and both proteins accumulate due to genotoxic stimuli, the cell cycle arrest might happen not in the G1 but in the G2 phase.
阿霉素(ADM)广泛用于膀胱癌的全身和局部治疗,可诱导膀胱癌细胞凋亡。在此,我们研究了阿霉素对具有不同p53和p21(WAF1/CIP1)状态的膀胱癌细胞系细胞周期进程及细胞周期调节蛋白表达的影响。采用流式细胞术分析T24、HT - 1376、RT4和SCaBER膀胱癌细胞系的细胞周期分布。通过免疫印迹法分析细胞周期调节蛋白。用阿霉素处理携带野生型p53和p21(WAF1/CIP1)的RT4细胞,诱导了这两种蛋白的表达及细胞周期停滞,但并非如预期的那样停滞在G1期,而是在G2期。同时,视网膜母细胞瘤(Rb)蛋白表达降低。作为E2F靶基因的增殖细胞核抗原(PCNA)的表达未发生变化。结果表明,即使肿瘤细胞携带野生型(wt)p53和wt p21(WAF1/CIP1),且这两种蛋白因基因毒性刺激而积累,细胞周期停滞也可能并非发生在G1期,而是在G2期。