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Super\u2010enhancers (SEs) are crucial epigenetic cis\u2010regulatory elements whose extensive reprogramming drives aberrant transcription in cancers. To study SE in GBC, the genomic distribution of H3K27ac is profiled in multiple GBC tissue and cell line samples to establish the SE landscape and its associated core regulatory circuitry (CRC). The biliary lineage factor SOX9 and Wnt pathway effector TCF7L2, two master transcription factor (TF) candidates identified by CRC analysis, are verified to co\u2010occupy each other's SE region, forming a mutually autoregulatory loop to drive oncogenic SE reprogramming in a subset of GBC. The SOX9\/TCF7L2 double\u2010high GBC cells are highly dependent on the two TFs and enriched of SE\u2010associated gene signatures related to stemness, ErbB and Wnt pathways. Patients with more such GBC cells exhibited significantly worse prognosis. Furthermore, SOX9\/TCF7L2 double\u2010high GBC preclinical models are found to be susceptible to SE\u2010targeted CDK7 inhibition therapy in vitro and in vivo. Together, this study provides novel insights into the epigenetic mechanisms underlying the oncogenesis of a subset of GBCs with poorer prognosis and illustrates promising prognostic stratification and therapeutic strategies for treating those GBC patients in future clinical trials.<\/jats:p>","DOI":"10.1002\/advs.202406448","type":"journal-article","created":{"date-parts":[[2024,11,4]],"date-time":"2024-11-04T04:45:07Z","timestamp":1730695507000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":6,"title":["Super\u2010Enhancer Reprograming Driven by SOX9 and TCF7L2 Represents Transcription\u2010Targeted Therapeutic Vulnerability for Treating Gallbladder Cancer"],"prefix":"10.1002","volume":"11","author":[{"given":"Siyuan","family":"Yan","sequence":"first","affiliation":[{"name":"Department of Biliary\u2010Pancreatic Surgery Renji Hospital Affiliated to Shanghai Jiao Tong University School of Medicine  Shanghai 200120 P. R. 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