转录因子
癌症研究
间质细胞
谱系(遗传)
生物
细胞生物学
计算生物学
遗传学
基因
作者
Keun-Woo Lee,So-Young Yeo,Jeong-Ryeol Gong,Ok Jae Koo,Insuk Sohn,Woo Yong Lee,Hee Cheol Kim,Seong Hyeon Yun,Yong Beom Cho,Mi-Ae Choi,Sugyun An,Juhee Kim,Chang Ohk Sung,Kwang-Hyun Cho,Seok-Hyung Kim
标识
DOI:10.1038/s41467-022-30484-4
摘要
Although stromal fibroblasts play a critical role in cancer progression, their identities remain unclear as they exhibit high heterogeneity and plasticity. Here, a master transcription factor (mTF) constructing core-regulatory circuitry, PRRX1, which determines the fibroblast lineage with a myofibroblastic phenotype, is identified for the fibroblast subgroup. PRRX1 orchestrates the functional drift of fibroblasts into myofibroblastic phenotype via TGF-β signaling by remodeling a super-enhancer landscape. Such reprogrammed fibroblasts have myofibroblastic functions resulting in markedly enhanced tumorigenicity and aggressiveness of cancer. PRRX1 expression in cancer-associated fibroblast (CAF) has an unfavorable prognosis in multiple cancer types. Fibroblast-specific PRRX1 depletion induces long-term and sustained complete remission of chemotherapy-resistant cancer in genetically engineered mice models. This study reveals CAF subpopulations based on super-enhancer profiles including PRRX1. Therefore, mTFs, including PRRX1, provide another opportunity for establishing a hierarchical classification system of fibroblasts and cancer treatment by targeting fibroblasts.
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