自噬
急性早幼粒细胞白血病
生物
髓系白血病
癌症研究
分化疗法
造血
髓样
骨髓生成
细胞生物学
维甲酸
白血病
维甲酸
灯1
细胞分化
细胞培养
干细胞
免疫学
细胞凋亡
生物化学
基因
遗传学
作者
Sreoshee Rafiq,Irene Mungure,Yara Banz,Nicolas J. Niklaus,Thomas Kaufmann,Stefan Müller,Arnaud Jacquel,Guillaume Robert,Patrick Auberger,Bruce E. Torbett,Sylviane Muller,Mario P. Tschan,Magali Humbert
出处
期刊:Pharmacology
[S. Karger AG]
日期:2024-01-01
卷期号:109 (4): 216-230
摘要
Acute myeloid leukemia (AML) is a cancer of the hematopoietic system characterized by hyperproliferation of undifferentiated cells of the myeloid lineage. While most of AML therapies are focused toward tumor debulking, all-trans retinoic acid (ATRA) induces neutrophil differentiation in the AML subtype acute promyelocytic leukemia (APL). Macroautophagy has been extensively investigated in the context of various cancers and is often dysregulated in AML where it can have context-dependent pro- or anti-leukemogenic effects. On the contrary, the implications of chaperone-mediated autophagy (CMA) on the pathophysiology of diseases are still being explored and its role in AML remains elusive.
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