Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5658561 | Gastroenterology | 2017 | 59 Pages |
Abstract
In rodent HSCs and TICs, we found SCD expression to be regulated by Wnt-β-catenin signaling, and MUFAs produced by SCD provided a forward loop to amplify Wnt signaling via stabilization of Lrp5 and Lrp6 mRNAs, contributing to liver fibrosis and tumor growth. SCD expressed by HSCs promoted liver tumor development in mice. Components of the identified loop linking HSCs and TICs might be therapeutic targets for liver fibrosis and tumors.
Keywords
TICDVLBSCCCl4MUFAPPARDenGSK3stearoyl-CoA desaturaseBDLHepatocarcinogenesisPalmitoleateSREBP-1ACTA2AKT serine/threonine kinase 1NF-Ynuclear transcription factor YHSCshRNAqPCRPOAmRNAGFPSCDLRPDkk-1HCCMOImessenger RNAshort hairpin RNAAdenovirusAktStearatemonounsaturated fatty acidILKOleateα-smooth muscle actinchromatin immunoprecipitationdisheveleddiethylnitrosamineHepatic stellate cellCancer stem cellspalmitateAU-rich elementUTR یا untranslated regions untranslated regionKnockdownAREHepatitis C virusHCVquantitative polymerase chain reactionSterol regulatory element binding protein 1green fluorescent proteinlow density lipoprotein receptor-related proteinbile duct ligationmultiplicity of infectionHuRCHiPHepatocellular carcinomaCarbon tetrachlorideintegrin-linked kinaseglycogen synthase kinase 3peroxisome proliferator-activated receptor
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Authors
Keane K.Y. Lai, Soo-Mi Kweon, Feng Chi, Edward Hwang, Yasuaki Kabe, Reiichi Higashiyama, Lan Qin, Rui Yan, Raymond P. Wu, Keith Lai, Naoaki Fujii, Samuel French, Jun Xu, Jian-Ying Wang, Ramachandran Murali, Lopa Mishra, Ju-Seog Lee, James M. Ntambi,