The origin of hepatocellular carcinoma is regulated by metabolic zonation [RNA-seq]

The origin of cancer is poorly understood because premalignant cells are rarely followed in their native environments. While the spatial compartmentalization of metabolic functions is critical for proper liver function, it is unknown if cancers arise from some zones but not others, and if there are metabolic determinants of cancer risk. Zone-specific, mosaic introduction of Ctnnb1 and Arid2 mutations, commonly co-mutated genes in hepatocellular carcinoma (HCC), showed that position and metabolic context determine clone fates. Ctnnb1/Arid2-driven cancers were much more likely to arise in zone 3. The zone 3 genes Gstm2 and Gstm3 were required for efficient HCC initiation, in part through inhibition of ferroptosis. In the liver, the zonal determinants of HCC development can reveal metabolic vulnerabilities of cancer. Overall design: Genetic mouse models with zone-specific CreER were given tamoxifen at P28 to induce zone-specific tumor drivers and followed for 6-12 months post-tamoxifen for tumor formation. WT C57/BL6 mice used for controls were treated with AAV-Cre and were maintained on normal chow diet for up to 12 months.