平方毫米
三阴性乳腺癌
癌症研究
细胞凋亡
靶向治疗
癌症
生物
蛋白酶体抑制剂
下调和上调
乳腺癌
基因
遗传学
作者
Clare M. Adams,Ramkrishna Mitra,You‐Cai Xiao,Peter Michener,Juan Palazzo,Allen Chao,Jitendra Gour,Joel Cassel,Joseph M. Salvino,Christine M. Eischen
出处
期刊:Cancer Discovery
[American Association for Cancer Research]
日期:2023-02-03
卷期号:13 (5): 1210-1229
被引量:94
标识
DOI:10.1158/2159-8290.cd-22-1131
摘要
p53-inactivated TNBC is an aggressive, therapy-resistant, and lethal breast cancer subtype. We designed a new compound targeting an unexpected vulnerability we identified in TNBC. Our MDM2-targeted degrader kills p53-inactivated TNBC cells, highlighting the requirement for MDM2 in TNBC cell survival and as a new therapeutic target for this disease. See related commentary by Peuget and Selivanova, p. 1043. This article is highlighted in the In This Issue feature, p. 1027.
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