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Identification of a tumor-suppressive human-specific microRNA within the FHIT tumor-suppressor gene.
Hu, Baocheng; Ying, Xiaomin; Wang, Jian; Piriyapongsa, Jittima; Jordan, I King; Sheng, Jipo; Yu, Fang; Zhao, Po; Li, Yazhuo; Wang, Hongyan; Ng, Wooi Loon; Hu, Shuofeng; Wang, Xiang; Wang, Chenguang; Zheng, Xiaofei; Li, Wuju; Curran, Walter J; Wang, Ya.
Afiliação
  • Hu B; Authors' Affiliations: Department of Medical Molecular Biology, Beijing Institute of Biotechnology; Center of Computational Biology, Beijing Institute of Basic Medical Sciences; Department of Pathology, Chinese PLA General Hospital; Department of Biochemistry and Molecular Biology, Beijing Institute of Radiation Medicine, Beijing, China; Department of Radiation Oncology, Emory University School of Medicine, Winship Cancer Institute of Emory University; School of Biology, Georgia Institute of Tec
Cancer Res ; 74(8): 2283-94, 2014 Apr 15.
Article em En | MEDLINE | ID: mdl-24556720
ABSTRACT
Loss or attenuated expression of the tumor-suppressor gene FHIT is associated paradoxically with poor progression of human tumors. Fhit promotes apoptosis and regulates reactive oxygen species; however, the mechanism by which Fhit inhibits tumor growth in animals remains unclear. In this study, we used a multidisciplinary approach based on bioinformatics, small RNA library screening, human tissue analysis, and a xenograft mouse model to identify a novel member of the miR-548 family in the fourth intron of the human FHIT gene. Characterization of this human-specific microRNA illustrates the importance of this class of microRNAs in tumor suppression and may influence interpretation of Fhit action in human cancer.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes Supressores de Tumor / Hidrolases Anidrido Ácido / MicroRNAs / Proteínas de Neoplasias Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Genes Supressores de Tumor / Hidrolases Anidrido Ácido / MicroRNAs / Proteínas de Neoplasias Idioma: En Ano de publicação: 2014 Tipo de documento: Article