IDH1
异柠檬酸脱氢酶
髓系白血病
癌症研究
癌症干细胞
生物
癌变
突变体
癌症
干细胞
白血病
细胞分化
癌细胞
软骨肉瘤
免疫学
细胞生物学
酶
医学
遗传学
生物化学
病理
基因
作者
Remco J. Molenaar,Johanna W. Wilmink
标识
DOI:10.1369/00221554211062499
摘要
Isocitrate dehydrogenase 1 and 2 (IDH1/2) are enzymes recurrently mutated in various types of cancer, including glioma, cholangiocarcinoma, chondrosarcoma, and acute myeloid leukemia. Mutant IDH1/2 induce a block in differentiation and thereby contribute to the stemness and oncogenesis of their cells of origin. Recently, small-molecule inhibitors of mutant IDH1/2 have been Food and Drug Administration–approved for the treatment of IDH1/2-mutated acute myeloid leukemia. These inhibitors decrease the stemness of the targeted IDH1/2-mutated cancer cells and induce their differentiation to more mature cells. In this review, we elucidate the mechanisms by which mutant IDH1/2 induce a block in differentiation and the biological and clinical effects of the release into differentiation by mutant-IDH1/2 inhibitors. (J Histochem Cytochem 70:83–97, 2022)
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