重编程
细胞分化
分化疗法
癌症
程序性细胞死亡
疾病
癌细胞
细胞凋亡
癌症治疗
癌症研究
细胞疗法
细胞
医学
生物
生物信息学
细胞培养
内科学
生物化学
遗传学
急性早幼粒细胞白血病
基因
维甲酸
作者
Magdalena Leszczyniecka,Thomas M. Roberts,Paul Dent,Steven Grant,Paul B. Fisher
标识
DOI:10.1016/s0163-7258(01)00132-2
摘要
Current cancer therapies are highly toxic and often nonspecific. A potentially less toxic approach to treating this prevalent disease employs agents that modify cancer cell differentiation, termed ‘differentiation therapy.’ This approach is based on the tacit assumption that many neoplastic cell types exhibit reversible defects in differentiation, which upon appropriate treatment, results in tumor reprogramming and a concomitant loss in proliferative capacity and induction of terminal differentiation or apoptosis (programmed cell death). Laboratory studies that focus on elucidating mechanisms of action are demonstrating the effectiveness of ‘differentiation therapy,’ which is now beginning to show translational promise in the clinical setting.
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