Advances in New Targets for Differentiation Therapy of Acute Myeloid Leukemia

J. Yao, Mengjie Zhao, Jiang-An Wang, Liuya Wei
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引用次数: 1

Abstract

Acute myeloid leukemia (AML) is a clinical and genetic heterogeneous disease with a poor prognosis. Recent advances in genomics and molecular biology have immensely improved the understanding of disease. The advantages of syndrome differentiation and treatment are strong selectivity, good curative effect and lesser side effects. In recent years, according to the molecular mechanism of acute myeloid leukemia, many new therapeutic targets have been found. New targets of differentiation therapy in recent years, such as cell cyclin-dependent kinase (CDK2), isocitrate dehydrogenase (IDH1, IDH2), Homeobox genes (HoxA9), Dihy-droorotate dehydrogenase (DHODH) and some others, are reviewed in this article.
急性髓系白血病分化治疗新靶点的研究进展
急性髓细胞白血病(AML)是一种临床和遗传异质性疾病,预后较差。基因组学和分子生物学的最新进展极大地提高了人们对疾病的理解。辨证论治的优点是选择性强,疗效好,副作用小。近年来,根据急性粒细胞白血病的分子机制,发现了许多新的治疗靶点。本文综述了近年来分化治疗的新靶点,如细胞周期蛋白依赖性激酶(CDK2)、异柠檬酸脱氢酶(IDH1,IDH2)、同源框基因(HoxA9)、二氢脱水脱氢酶(DHODH)等。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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