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P53基因对K562细胞增殖的影响 被引量:1

Effects of p53 gene on K562 cell line proliferation
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摘要 目的 观察恢复K5 6 2细胞的p5 3蛋白功能后该细胞的生物学行为的改变 ,探索用野生型p5 3基因治疗白血病的可能性。方法 以K5 6 2细胞为研究对象 ,电穿孔法转导野生型p5 3基因 ,RT PCR和免疫细胞化学方法检测p5 3基因的表达 ,3H TdR掺入法检测细胞增殖 ,用流式细胞仪分别以TUNEL、annexin V、细胞周期检测细胞的凋亡情况和细胞周期分布情况。结果 转染p5 3基因的K5 6 2细胞 ,出现明显细胞周期G1 期停滞 ,增殖抑制率为 2 4 .17% ,但用TUNEL、annexin V和亚二倍体峰检测未发现与未转染p5 3基因组有凋亡细胞比例差异。结论 P5 3基因对K5 6 2细胞有一定的治疗效应 。 Objective To investigate effects of p53 gene on proliferation and apoptosis in K562 cell line. Methods P53 gene was transferred to monoclonal K562 cells with electroporation. P53 gene transcription and expression were detected with RT- PCR and immunocytochemical staining. Proliferation test was conducted by using 3 H-thymidine ( 3 H-TdR) incorporation assay, and apoptosis was analyzed by TUNEL, annexin V and hypodiploid apex. Results Compared with wild type K562 and neo-K562, proliferation of p53-K562 decreased by 24.17% and exhibited G 1 arrest. Significant apoptosis did not occur. Conclusion P53 gene could induce less proliferation and G1 arrest but not apoptosis.
出处 《免疫学杂志》 CAS CSCD 北大核心 2004年第2期106-109,共4页 Immunological Journal
基金 重庆市科委攻关项目 (1 998- 1 9- 2 7)
关键词 P53 K562细胞 细胞增殖 细胞凋亡 P53 K562 cell line Cell proliferation Cell apoptosis
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  • 1Weller M. Predicting response to cancer chemotherapy: the role of P53 [J]. Cell Tissue Res, 1998, 292 (3): 435 - 445.
  • 2Agarwal ML, Taylor WR, Chernov MV, et al. The P53 network [J]. J Biol Chem, 1998, 273 (1): 1-4.
  • 3Joseph B, Lewensohn R, Zhivotovsky B. Role of apoptosis in the response of lung carcinomas to ant-cancer treatment [J].Ann N Y Acad Sci, 2000, 926:204 - 216.
  • 4Chang WT, Kang JJ, Lee KY, et al. Triptolide and chemotherapy cooperate in tumor cell apoptosis. A role for the P53pathway [J]. J Bio Chem, 2001, 276 (3): 2 221 - 2 227.
  • 5李仁,任碧轩,杨晓红,任碧清,左祖英,赵明才,唐恩洁.重组P_(53)基因表达及其与Fas关系初探[J].川北医学院学报,1998,13(2):1-3. 被引量:2
  • 6任碧轩,李仁,冯莉,唐恩洁,杨晓红,赵明才,杨健,张紫福,张艳艳,魏祥云.重组P_(53)基因在HepG-2中的表达及作用[J].川北医学院学报,1999,14(2):1-4. 被引量:2

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