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急性早幼粒细胞白血病诱导分化的分子机制

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摘要 急性早幼粒细胞白血病(APL)以异常早幼粒细胞异常增殖伴分化受阻为特点,>95%的患者有t(15;17)/PML-RARα融合基因,全反式维甲酸(ATRA)为APL特异相关基因的靶向治疗药物。近年来对ATRA诱导APL分化的分子机制有了一些新的认识。本文就细胞内PKC、cAMP/PKA信号途径、维甲酸受体、融合蛋白、核体、端粒酶、细胞周期与癌基因等方面的研究进展进行综述。
出处 《国外医学(输血及血液学分册)》 2004年第6期500-503,共4页 Foreign Medical Sciences(Section of Blood Transfusion and Heanatology)
基金 天津市科委自然科学基金(013615611)
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