Network Analysis Identifies Regulators of Basal-Like Breast Cancer Reprogramming and Endocrine Therapy Vulnerability

被引:27
作者
Choi, Sea R. [1 ]
Hwang, Chae Young [1 ]
Lee, Jonghoon [1 ]
Cho, Kwang-Hyun [1 ]
机构
[1] Korea Adv Inst Sci & Technol KAIST, Dept Bio & Brain Engn, Daejeon, South Korea
基金
新加坡国家研究基金会;
关键词
TRANSCRIPTION FACTOR BCL11A; ESTROGEN-RECEPTOR; EXPRESSION; EGFR; RESISTANCE; REPRESSOR; RISK;
D O I
10.1158/0008-5472.CAN-21-0621
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Basal-like breast cancer is the most aggressive breast cancer subtype with the worst prognosis. Despite its high recurrence rate, chemotherapy is the only treatment for basal-like breast cancer, which lacks expression of hormone receptors. In contrast, luminal A tumors express ERa and can undergo endocrine therapy for treatment. Previous studies have tried to develop effective treatments for basal-like patients using various therapeutics but failed due to the complex and dynamic nature of the disease. In this study, we performed a transcriptomic analysis of patients with breast cancer to construct a simplified but essential molecular regulatory network model. Network control analysis identified potential targets and elucidated the underlying mechanisms of reprogramming basal-like cancer cells into luminal A cells. Inhibition of BCL11A
引用
收藏
页码:320 / 333
页数:14
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