Core transcriptional regulatory circuitries in cancer

被引:48
作者
Chen, Ye [1 ]
Xu, Liang [1 ,2 ,3 ]
Lin, Ruby Yu-Tong [1 ]
Muschen, Markus [2 ]
Koeffler, H. Phillip [1 ,4 ,5 ]
机构
[1] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117599, Singapore
[2] City Hope Comprehens Canc Ctr, Dept Syst Biol, Monrovia, CA 91016 USA
[3] Zhejiang Univ, Coll Life Sci, Hangzhou 310058, Peoples R China
[4] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
[5] Natl Univ Singapore Hosp, Natl Univ Canc Inst, Singapore 119074, Singapore
基金
新加坡国家研究基金会; 英国惠康基金; 英国医学研究理事会;
关键词
SUPER-ENHANCERS; TAL1; COMPLEX; NETWORK; IDENTITY; ELEMENTS; AMPLIFICATION; PLURIPOTENCY; ACETYLATION; LANDSCAPE; PROGRAM;
D O I
10.1038/s41388-020-01459-w
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Transcription factors (TFs) coordinate the on-and-off states of gene expression typically in a combinatorial fashion. Studies from embryonic stem cells and other cell types have revealed that a clique of self-regulated core TFs control cell identity and cell state. These core TFs form interconnected feed-forward transcriptional loops to establish and reinforce the cell-type-specific gene-expression program; the ensemble of core TFs and their regulatory loops constitutes core transcriptional regulatory circuitry (CRC). Here, we summarize recent progress in computational reconstitution and biologic exploration of CRCs across various human malignancies, and consolidate the strategy and methodology for CRC discovery. We also discuss the genetic basis and therapeutic vulnerability of CRC, and highlight new frontiers and future efforts for the study of CRC in cancer. Knowledge of CRC in cancer is fundamental to understanding cancer-specific transcriptional addiction, and should provide important insight to both pathobiology and therapeutics.
引用
收藏
页码:6633 / 6646
页数:14
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