铁代谢与细胞周期调控的研究进展
Iron metabolism and cell cycle regulation and control of Progress
铁是细胞分裂增殖必需的微量元素,铁参与细胞内DNA合成,以保证细胞从G1期顺利进入S期. 铁代谢紊乱则会引起细胞周期发生改变而造成细胞凋亡。正常的铁水平可以通过激活细胞因子和细胞周期依赖激酶 cyclin-dependent kinases (cdks) 促进细胞DNA的合成和周期蛋白表达,细胞得以分裂增殖。肿瘤细胞分裂需要大量的铁,如果用铁螯合剂处理肿瘤细胞,可使细胞内铁水平降低,提高p53表达,造成细胞S期阻滞或者促使肿瘤细胞凋亡。因此研究铁代谢机理与细胞周期调控的关系对于防治肿瘤的发生发展具有重要的理论和现实意义。
Iron is an essential trace Element for cell proliferation; iron is involved in process of DNA synthesis to ensure the cells have a smooth transition from G1 phase to S phase. Iron metabolism disorders can cause the cell cycle changes even cell apoptosis. Normal levels of iron can activate cytokines and cell cycle-dependent kinase cyclin-dependent kinases (cdks) to promote the synthesis of DNA and cell cycle protein expression, and this can make sure that the cells can proliferate smoothly. Tumor cells' proliferation requires a large amount of iron, iron chelating can reduce the iron content of tumor cells and enhance the expression of p53, causing the cells stopped in the S phage or apoptosis. Study the mechanism between iron metabolism and cell cycle regulation has great theoretical and practical significance.
赵昭、常彦忠、段相林
基础医学肿瘤学细胞生物学
铁细胞周期细胞周期蛋白细胞周期依赖激酶铁螯合剂
ironcell cyclecell cycle proteincyclin-dependent kinasesiron chelating agents
赵昭,常彦忠,段相林.铁代谢与细胞周期调控的研究进展[EB/OL].(2011-03-22)[2025-07-22].http://www.paper.edu.cn/releasepaper/content/201103-867.点此复制
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