Molecular Oncology, PSL Research University, CNRS, UMR 144, Institut Curie, Equipe Labellisée Ligue Nationale Contre le Cancer, Paris, France.
Sorbonne Universités, UPMC Université Paris 06, CNRS, UMR144, 75005, Paris, France.
Oncogene. 2023 May;42(19):1524-1542. doi: 10.1038/s41388-023-02662-1. Epub 2023 Mar 22.
Muscle-invasive bladder cancer (BLCA) is an aggressive disease. Consensus BLCA transcriptomic subtypes have been proposed, with two major Luminal and Basal subgroups, presenting distinct molecular and clinical characteristics. However, how these distinct subtypes are regulated remains unclear. We hypothesized that epigenetic activation of distinct super-enhancers could drive the transcriptional programs of BLCA subtypes. Through integrated RNA-sequencing and epigenomic profiling of histone marks in primary tumours, cancer cell lines, and normal human urothelia, we established the first integrated epigenetic map of BLCA and demonstrated the link between subtype and epigenetic control. We identified the repertoire of activated super-enhancers and highlighted Basal, Luminal and Normal-associated SEs. We revealed super-enhancer-regulated networks of candidate master transcription factors for Luminal and Basal subgroups including FOXA1 and ZBED2, respectively. FOXA1 CRISPR-Cas9 mutation triggered a shift from Luminal to Basal phenotype, confirming its role in Luminal identity regulation and induced ZBED2 overexpression. In parallel, we showed that both FOXA1 and ZBED2 play concordant roles in preventing inflammatory response in cancer cells through STAT2 inhibition. Our study furthers the understanding of epigenetic regulation of muscle-invasive BLCA and identifies a co-regulated network of super-enhancers and associated transcription factors providing potential targets for the treatment of this aggressive disease.
肌层浸润性膀胱癌(BLCA)是一种侵袭性疾病。目前已经提出了共识性 BLCA 转录组亚型,其中包括两个主要的 Luminal 和基底亚型,它们具有不同的分子和临床特征。然而,这些不同亚型是如何被调控的仍然不清楚。我们假设,不同超级增强子的表观遗传激活可以驱动 BLCA 亚型的转录程序。通过对原发肿瘤、癌细胞系和正常人类尿路上皮进行 RNA-seq 和组蛋白标记的表观基因组分析,我们建立了 BLCA 的首个综合表观遗传图谱,并证明了亚型与表观遗传控制之间的联系。我们确定了激活超级增强子的 repertoire,并强调了基底、Luminal 和正常相关的 SEs。我们揭示了候选主转录因子的超级增强子调控网络,这些因子分别为 Luminal 和基底亚群,包括 FOXA1 和 ZBED2。FOXA1 CRISPR-Cas9 突变引发了从 Luminal 到基底表型的转变,证实了其在 Luminal 身份调控中的作用,并诱导了 ZBED2 的过表达。同时,我们表明,FOXA1 和 ZBED2 都通过抑制 STAT2 在癌细胞中发挥协同作用,防止炎症反应。我们的研究进一步了解了肌层浸润性 BLCA 的表观遗传调控,并确定了超级增强子和相关转录因子的共同调控网络,为治疗这种侵袭性疾病提供了潜在的靶点。