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作 者:刘春生[1] 孔北华[1] 马道新[1] 姜洁[1] 李学汤[2]
机构地区:[1]山东大学齐鲁医院,250012 [2]中国医学科学院肿瘤研究所
出 处:《现代妇产科进展》2000年第6期428-431,共4页Progress in Obstetrics and Gynecology
摘 要:研究 p53基因导入已知内源背景的肿瘤 MDR细胞所致的恶性表型和MDR表型的改变及两者的关系。方法:用磷酸钙沉淀法将含有野生型及全长反义 p53cDNA的逆转录病毒载体pDWp53及 pDAp53转染病毒包装细胞 PA317,测定病毒滴度。用此病毒感染卵巢癌多药耐药细胞株A2780/ADM,Southern Blot鉴定,检测转导基因后细胞株的恶性度、多药耐药性等情况。结果:野生型及反义全长p53cDNA均转入 PA317细胞获得效价为(1- 1.5) X105CFU/ml的前病毒,以此感染卵巢癌多药耐药细胞株A2780/ADM,Southem Blot证实p53基因导入该细胞并整合到基因组DNA中,进一步测试观察到:①导入野生型p53基因的A2780/ADM细胞生长被抑制、恶性度降低,细胞形态和生长曲线改变,软琼脂集落形成率及裸鼠接种成瘤率降低;②细胞多药耐药性减弱,对ADM耐药性下降,P-gp表达降低;③反义p53的导入也对A2780/ADM恶性度有一定的影响;④野生型p53导致的MDR细胞恶性表型与MDR水平的降低似有平行关系。结论:p53基因对肿瘤细胞mdr- 1基因的表达可能起调控作用,p53发生突变的 M?Objective:To study the changes of tumor MDR cell malignant and MDR phenotype caused by transferring into p53 and to explore the relationship between them. Methods:Wild and anti - sense p53 were transfected into ovarian cancer MDR cell strain A2780/ADM was transferred by retrovirus vector and were the virus titre detected . The virus was infected into tumor MDR cell - A2780/ADM. After certificated by Southern blot, its ma- lignancy and multi-drug resistence was detectal. Results: After transfecting wild and anti - sense p53 into ovarian cancer MDR cell strain A2780/ADM by retrovirus vector, the fol- lowing result can be ovserved. The growth of the A2780/ADM cells were inhibited and their malignant degree and nude mice tumor - forming rate became lower. Cellular MDR was less- ened such as the reduction of the resistant ability to ADM and the lowering of the expression of P - gp. Transfection of anti - sense p53 can also influence the malignant degree of A2780/ADM. The malignant phenotype of MDR cells caused by the transfection of WT p53 seems parallelable to the lowering of MDR level. Conclusions: p53 may regulate the expres- sion of tumor cell mdr- 1 gene and MDR phenotype of the p53 mutant. MDR cells trans- fected with wild p53 can be reversed to such a degree which provides direct experimental ev- idence for reversing MDR at molecular level by transfecting p53 into cancer cell.
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