重编程
干细胞
癌症研究
医学
EZH2型
酪氨酸激酶
酪氨酸激酶抑制剂
造血
表观遗传学
免疫学
生物
内科学
癌症
细胞
细胞生物学
基因
受体
生物化学
遗传学
作者
Mary T. Scott,Koorosh Korfi,Peter Saffrey,Lisa Hopcroft,Ross Kinstrie,Francesca Pellicano,Carla Guenther,Paolo Gallipoli,Michelle Cruz,Karen Dunn,Heather G. Jørgensen,Jennifer Cassels,Ashley Hamilton,Andrew Crossan,Amy Sinclair,Tessa L. Holyoake,David Vetrie
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2016-09-14
卷期号:6 (11): 1248-1257
被引量:132
标识
DOI:10.1158/2159-8290.cd-16-0263
摘要
In CML, TKI-persistent LSCs remain an obstacle to cure, and approaches to eradicate them remain a significant unmet clinical need. We demonstrate that EZH2 and H3K27me3 reprogramming is important for LSC survival, but renders LSCs sensitive to the combined effects of EZH2i and TKI. This represents a novel approach to more effectively target LSCs in patients receiving TKI treatment. Cancer Discov; 6(11); 1248-57. ©2016 AACR.See related article by Xie et al., p. 1237This article is highlighted in the In This Issue feature, p. 1197.
科研通智能强力驱动
Strongly Powered by AbleSci AI