Ghazimoradi Mohammad H, Babashah Sadegh
Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Cell Death Discov. 2025 Apr 11;11(1):164. doi: 10.1038/s41420-025-02438-4.
Cancer-associated fibroblasts (CAFs) are pivotal drivers of tumor progression, yet the molecular mechanisms underlying their activation remain incompletely understood. Here, we identified the TET1/SMAD4/GATA6 regulatory axis as a central mechanism governing CAF transformation and function in breast cancer. Through integrative in vitro and in vivo models, we demonstrated that TET1, an epigenetic modulator, demethylates the SMAD4 promoter, enhancing SMAD4 expression. SMAD4 transcriptionally upregulates GATA6, which amplifies TGF-β signaling by directly activating the TGF-β promoter, establishing a self-reinforcing feedforward loop critical for CAF identity and stromal-tumor crosstalk. GATA6 and TET1 were significantly upregulated in breast CAFs compared to normal fibroblasts (NFs) and TGF-β-induced CAFs. Loss- or gain-of-function experiments revealed that these regulators control CAF survival, marker expression, and secretion of pro-tumorigenic factors. Knockdown of GATA6 or TET1 reduced CAF-mediated migration and invasion of breast cancer cells in vitro, while their overexpression enhanced cancer cell aggressiveness. Mechanistically, TET1-mediated epigenetic remodeling and GATA6-driven transcriptional activation converge on the TGF-β/SMAD pathway, sustaining CAF activation. In vivo, tumors derived from GATA6- or TET1-depleted CAFs exhibited reduced growth, proliferation, and CAF engraftment, underscoring their role in tumor progression. These findings position GATA6 and TET1 as promising targets to disrupt CAF-driven tumorigenesis, offering novel strategies for breast cancer treatment. By unraveling the epigenetic-transcriptional interplay within the tumor microenvironment, this study advances our understanding of stromal reprogramming and its implications for precision oncology.
癌症相关成纤维细胞(CAFs)是肿瘤进展的关键驱动因素,但其激活背后的分子机制仍未完全明确。在此,我们确定了TET1/SMAD4/GATA6调控轴是乳腺癌中控制CAF转化和功能的核心机制。通过整合的体外和体内模型,我们证明了作为一种表观遗传调节剂的TET1使SMAD4启动子去甲基化,增强了SMAD4的表达。SMAD4转录上调GATA6,后者通过直接激活TGF-β启动子来放大TGF-β信号,从而建立了一个对CAF特性和基质-肿瘤相互作用至关重要的自我强化前馈回路。与正常成纤维细胞(NFs)和TGF-β诱导的CAFs相比,GATA6和TET1在乳腺CAFs中显著上调。功能缺失或功能获得实验表明,这些调节因子控制CAF的存活、标志物表达以及促肿瘤因子的分泌。敲低GATA6或TET1可降低体外CAF介导的乳腺癌细胞迁移和侵袭,而它们的过表达则增强了癌细胞的侵袭性。从机制上讲,TET1介导的表观遗传重塑和GATA6驱动的转录激活都集中在TGF-β/SMAD途径上,维持CAF的激活。在体内,源自GATA6或TET1缺失的CAFs的肿瘤生长、增殖和CAF植入均减少,突出了它们在肿瘤进展中的作用。这些发现将GATA6和TET1定位为破坏CAF驱动的肿瘤发生的有前景的靶点,为乳腺癌治疗提供了新策略。通过揭示肿瘤微环境中的表观遗传-转录相互作用,本研究推进了我们对基质重编程及其对精准肿瘤学影响的理解。