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miR-149* Suppresses Liver Cancer Progression by Down-Regulating Tumor Necrosis Factor Receptor 1-Associated Death Domain Protein Expression.
Feng, Qingqing; Zhang, Hongli; Nie, Xiaobo; Li, Yuanqiang; Chen, Wei-Dong; Wang, Yan-Dong.
Affiliation
  • Feng Q; State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, PR China.
  • Zhang H; State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, PR China.
  • Nie X; Key Laboratory of Receptors-Mediated Gene Regulation and Drug Discovery, School of Medicine, Henan University, Kaifeng, PR China.
  • Li Y; State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, PR China.
  • Chen WD; Key Laboratory of Receptors-Mediated Gene Regulation and Drug Discovery, School of Medicine, Henan University, Kaifeng, PR China; Key Laboratory of Molecular Pathology, School of Basic Medical Science, Inner Mongolia Medical University, Hohhot, PR China. Electronic address: wdchen666@163.com.
  • Wang YD; State Key Laboratory of Chemical Resource Engineering, College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, PR China. Electronic address: ydwangbuct2009@163.com.
Am J Pathol ; 190(2): 469-483, 2020 02.
Article in En | MEDLINE | ID: mdl-31783009
ABSTRACT
Liver cancer is the third leading cause of cancer-related death worldwide. Herein, we show that miR-149* serves as a novel tumor suppressor for liver tumorigenesis. Mice with genetic deletion of miR-149* (miR-149*-/- mice), which caused loss of both miR-149 and miR-149*, were considerably more susceptible to acute liver injury and hepatic carcinogenesis induced by diethylnitrosamine than wild-type mice, accompanied by increased compensatory proliferation and up-regulated gene expression of certain inflammatory cytokines. miR-149* mimics dramatically impaired liver cancer cell proliferation and migration in vitro and blocked liver cancer progression in a xenograft model. Furthermore, miR-149* strongly suppressed NF-κB signaling and repressed tumor necrosis factor receptor type 1-associated death domain protein expression in the NF-κB signaling pathway. These results reveal that miR-149*, as a novel liver tumor suppressor, may serve as a potential therapeutic target for liver cancer treatment.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Gene Expression Regulation, Neoplastic / NF-kappa B / MicroRNAs / TNF Receptor-Associated Death Domain Protein / Liver Neoplasms, Experimental Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: Am J Pathol Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biomarkers, Tumor / Gene Expression Regulation, Neoplastic / NF-kappa B / MicroRNAs / TNF Receptor-Associated Death Domain Protein / Liver Neoplasms, Experimental Type of study: Prognostic_studies / Risk_factors_studies Limits: Animals Language: En Journal: Am J Pathol Year: 2020 Document type: Article