TY - JOUR T1 - Histone H3K27 demethylase KDM6A is an epigenetic gatekeeper of mTORC1 signalling in cancer JF - Gut JO - Gut DO - 10.1136/gutjnl-2021-325405 SP - gutjnl-2021-325405 AU - Steffie Revia AU - Agnieszka Seretny AU - Lena Wendler AU - Ana Banito AU - Christoph Eckert AU - Kersten Breuer AU - Anand Mayakonda AU - Pavlo Lutsik AU - Matthias Evert AU - Silvia Ribback AU - Suchira Gallage AU - Ismaiel Chikh Bakri AU - Kai Breuhahn AU - Peter Schirmacher AU - Stefan Heinrich AU - Matthias M Gaida AU - Mathias Heikenwälder AU - Diego F Calvisi AU - Christoph Plass AU - Scott W Lowe AU - Darjus F Tschaharganeh Y1 - 2021/09/11 UR - http://gut.bmj.com/content/early/2021/09/11/gutjnl-2021-325405.abstract N2 - Objective Large-scale genome sequencing efforts of human tumours identified epigenetic modifiers as one of the most frequently mutated gene class in human cancer. However, how these mutations drive tumour development and tumour progression are largely unknown. Here, we investigated the function of the histone demethylase KDM6A in gastrointestinal cancers, such as liver cancer and pancreatic cancer.Design Genetic alterations as well as expression analyses of KDM6A were performed in patients with liver cancer. Genetic mouse models of liver and pancreatic cancer coupled with Kdm6a-deficiency were investigated, transcriptomic and epigenetic profiling was performed, and in vivo and in vitro drug treatments were conducted.Results KDM6A expression was lost in 30% of patients with liver cancer. Kdm6a deletion significantly accelerated tumour development in murine liver and pancreatic cancer models. Kdm6a-deficient tumours showed hyperactivation of mTORC1 signalling, whereas endogenous Kdm6a re-expression by inducible RNA-interference in established Kdm6a-deficient tumours diminished mTORC1 activity resulting in attenuated tumour progression. Genome-wide transcriptional and epigenetic profiling revealed direct binding of Kdm6a to crucial negative regulators of mTORC1, such as Deptor, and subsequent transcriptional activation by epigenetic remodelling. Moreover, in vitro and in vivo genetic epistasis experiments illustrated a crucial function of Deptor and mTORC1 in Kdm6a-dependent tumour suppression. Importantly, KDM6A expression in human tumours correlates with mTORC1 activity and KDM6A-deficient tumours exhibit increased sensitivity to mTORC1 inhibition.Conclusion KDM6A is an important tumour suppressor in gastrointestinal cancers and acts as an epigenetic toggle for mTORC1 signalling. Patients with KDM6A-deficient tumours could benefit of targeted therapy focusing on mTORC1 inhibition.Data are available in a public, open access repository. Data are available upon reasonable request. Memorial Sloan Kettering Cancer Center, ER -