We next evaluated the effects of KY19334 on hepatic fibrosis as a consequence of chronic liver injury using HFD + CCl4-model mice. Liver fibrosis monitored by the accumulation of α-Sma, collagen I, desmin, and Sirius … See more The administration of CCl4 combined with HFD induces chronic inflammation and oxidative stress, followed by liver fibrosis as in NASH28,29. The numbers of F4/80- and Cd11b-positive macrophages were apparently lower in … See more To elucidate the clinical implications of the role of CXXC5 in NASH development, we investigated the mRNA expression profiles of CXXC5 and Wnt-responsive genes in NASH patients with … See more To confirm the role of CXXC5 in the pathogenesis of NASH, Cxxc5+/+ and Cxxc5−/− mice were fed HFD + CCl4. The Cxxc5−/− mice exhibited lower body weight than the … See more As an approach to abolish CXXC5 function and determine its role in the pathological phenotypes of NASH, we examined the effects of KY19334, a small molecule that activates the Wnt/β … See more
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