摘要
目的探讨bcl2基因在人膀胱癌多药耐药中的作用。方法应用原位DNA末端转移酶标记法(TUNEL)、免疫细胞化学及逆转录多聚酶链式反应(RTPCR)技术,分别对阿霉素诱导的人膀胱癌耐药细胞株(BIU87/ADM)及敏感细胞株(BIU87)的细胞凋亡及其bcl2基因表达进行研究。结果(1)在相同条件下,与敏感细胞株相比,耐药细胞株中细胞凋亡明显受到抑制;(2)耐药细胞株中bcl2基因表达明显强于敏感细胞株。结论凋亡抑制基因bcl2在人膀胱癌多药耐药细胞中的高表达,是导致其细胞凋亡受抑制的重要原因,对于人膀胱癌多药耐药的产生具有重要意义。
Objective To evaluate the inhibition effect of liposome conjugated antisense oligonucleotides on the BIU 87 proliferation. Methods The human bladder cancer cell line BIU 87 was treated with antisense oligodeoxynucleotides targeting the mRNA encoding proliferating cell nuclear antigen (PCNA) with lipofectin.The inhibition of proliferation was studied with cell growth curves and MTT method.The expression of PCNA was detected immunohistochemically. Results The cell proliferation was inhibited effectively by antisense oligodeoxynucleotides with lipofectin ( P <0.05).The protein expression of PCNA was inhibited completely at 12 hours and effectively at 24 to 36 hours ( P <0.01).Lipofectin could enhance the effect by about 50 times.The sense oligodeoxynucleotides showed no such effect ( P <0.01). Conclusions Antisense oligodeoxynucleotides conjugated with lipofectin might be a hopeful method to inhibit the proliferation of bladder cancer cell by inhibiting the expression of PCNA.Further investigations are needed in order to use this method in bladder cancer therapy.
出处
《中华泌尿外科杂志》
CAS
CSCD
北大核心
1999年第4期234-236,共3页
Chinese Journal of Urology
关键词
膀胱肿瘤
多药耐药
BCL-2基因
药物疗法
Bladder neoplasms Proliferating cell nuclear antigen Liposomes Antisense oligodeoxynucleotide