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作 者:靳风烁[1] 方玉华[1] 于茂生[2] 惠宏襄[2] 辛建国[2] 金明
机构地区:[1]第三军医大学附属大坪医院泌尿外科 [2]第四军医大学附属西京医院泌尿外科
出 处:《第三军医大学学报》1997年第6期506-508,共3页Journal of Third Military Medical University
基 金:全军"八五"协作攻关课题
摘 要:目的:探讨cAMP诱导膀胱肿瘤细胞分化的作用。方法:野生型膀胱肿瘤细胞T24作为对照细胞,实验组细胞分别用10μmol/L和40μmol/L的cAMP诱导培养28d,观察对照细胞和实验细胞的增殖率、裸鼠致瘤率,流式细胞仪测定p21、p65蛋白表达率、电子显微镜观察细胞超微结构变化。结果:对照细胞增殖率、p21、p65表达率、裸鼠致瘤率均为100%。实验组细胞经10μmol/L和40μmol/L的8-Br-cAMP诱导14、21、28d,增殖率分别降为92.4、73.6、57.1、90.8、64.2、49.9%;10μmol/L和40μmol/L的cAMP诱导28d后,p21表达率分别降为63%和58%,p65表达率降为54%和49%,裸鼠致瘤率降为60%和40%;超微结构显示细胞恶性表型下降。结论:cAMP通过下调ras和myc基因表达而诱导分化、抑制肿瘤恶性表型,这一作用在肿瘤的预防和治疗中具有重要意义。Objective: To explore the inductive effects of cAMP on differentiation of bladder cancer cells. Methods: Wild type bladder cancer cell T24 was employed to serve as the control. The cells in the experimental group was respectively cultured with 10 μmol/L and 40 μmol/L of 8BrcAMP for 28 days. The proliferative rate and tumorigenic rate in nude mice were determined, the expressive rate of p21 and p65 protein measured with cytometry and the ultrastructural changes of all the cells observed with electron microscopy. Results: In the control group, the expressive rate of p21 and p65 protein and the proliferative rate and tumorigenic rate in nude mice of the cells were all 100%. In the experimental group, the proliferative rate of the cells were decreased to 92.4%, 73.6% and 57.1% and 90.8%, 64.2% and 49.9% in the 14th, 21th and 28th day after induction in 10 μmol/L and 40 μmol/L cAMP-induced cells respectively. In the 28th day after induction, the expressive rate of p21 was decreased to 63% and 58%, the expressive rate of p65 to 54% and 49% and the tumorigenic rate to nude mice to 60% and 40% in the cells induced by 10 μmol/L and 40 μmol/L cAMP respectively. Morphological observation showed that the malignant phenotype was inhibited. Conclusion: cAMP induces differentiation and inhibits the malignant phenotype of bladder cancer cells through downregulation of the expression of ras and myc genes, which is important for prevention and treatment of tumor.
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