造血
祖细胞
细胞生物学
干细胞
造血干细胞
生物
恶性转化
癌症研究
免疫学
作者
Dustin Carroll,Daret K. St. Clair
标识
DOI:10.1089/ars.2017.7326
摘要
Recent evidence demonstrates the potential for redox-based therapies to impact metabolic and epigenetic factors that could contribute to initial LSC transformation. This is balanced by the development of therapies that protect HSPC function. This pushes toward therapies that may alter the HSC/LSC redox state but lead to initiation cell fate signaling lost in malignant transformation while protecting normal HSPC function. Antioxid. Redox Signal.
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