髓系白血病
干细胞
舱室(船)
生物
白血病
癌症研究
髓样
癌症干细胞
细胞
基因表达
基因
细胞生物学
免疫学
遗传学
海洋学
地质学
作者
Karen Sachs,Aaron L. Sarver,Klara E. Noble-Orcutt,Rebecca S. LaRue,Marie Lue Antony,Daniel Chang,Yoonkyu Lee,Connor M. Navis,Alexandria L. Hillesheim,Ian R. Nykaza,Ngoc A. Ha,Conner J. Hansen,Fatma Keklik Karadağ,Rachel J. Bergerson,Michael R. Verneris,Matthew M. Meredith,Matthew Schomaker,Michael A. Linden,Chad L. Myers,David A. Largaespada
出处
期刊:Cancer Research
[American Association for Cancer Research]
日期:2019-11-29
卷期号:80 (3): 458-470
被引量:53
标识
DOI:10.1158/0008-5472.can-18-2932
摘要
Standard chemotherapy for acute myeloid leukemia (AML) targets proliferative cells and efficiently induces complete remission; however, many patients relapse and die of their disease. Relapse is caused by leukemia stem cells (LSC), the cells with self-renewal capacity. Self-renewal and proliferation are separate functions in normal hematopoietic stem cells (HSC) in steady-state conditions. If these functions are also separate functions in LSCs, then antiproliferative therapies may fail to target self-renewal, allowing for relapse. We investigated whether proliferation and self-renewal are separate functions in LSCs as they often are in HSCs. Distinct transcriptional profiles within LSCs of
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