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作 者:陈一招[1] 徐如祥[1] 张世忠[1] 邹玲[1]
机构地区:[1]第一军医大学珠江医院神经外科,广东广州510282
出 处:《第一军医大学学报》2000年第2期137-140,共4页Journal of First Military Medical University
基 金:国家自然科学基金!(39700143)
摘 要:目的探索p16基因在脑胶质瘤发生发展过程中的作用及其与脑胶质瘤细胞顺铂化疗敏感性的关系。方法采用脂质转染的方法.将外源野生型p16基因导入胶质瘤细胞株U251,观察p16基因长期稳定转染对胶质瘤细胞的作用,并筛选阳性克隆。同时以空载体质粒PCDNA3为对照。免疫组化、Northern杂交检测p16基因表达,对转染后细胞生长情况、细胞周期及细胞对顺铂(cis-diamminedichloroplatinum,CDDP)敏感性的变化进行分析。结果外源p16基因的高水平表达显著掏了胶质瘤U251细胞的生长,克隆形成率减少,克隆形成率减少,肿瘤细胞发生了G1期阻滞,同时,细胞对顺铂的敏感性降低,化疗药物诱导的凋亡细胞数减少。结论外源野生型p16基因可抑制胶质瘤细胞恶性增殖,同时降低U251细胞对顺铂的化疗敏感性。p16基因转染后对顺铂诱导凋亡作用的抑制可能是其主要机制。Objective To determine the effect of p16/CDK41 on the cell growth and the chemosensitivity of human glioma cells to cis-diamminedichloroplutinum (CDDP). Methods p16 gene was transfected into human glioma cell line U251 and the expression of exogenous p16 gene was examined. The effect of exogenous p16 gene on the cell growth and chemosensitivity of U251 to CDDP were eobserved. Results Expression of exogenous p16 gene inhibited the growth of U251 dramatically. GI arrest of tumor cells was observed after transfection. however, wild type p16-positive U251 cells were less sensitive to CDDP than control cells and the number of apoptotic cells following chemotherapy was reduced. Conclusion The expression of exogenous p16 gene can inhibit the growth of glioma cells, but paradoxically, the chemosensitivity of p16-positive glioma cells to CDDP is also decreased.
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