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LncRNA-NBAT-1 modulates esophageal cancer proliferation via PKM2.
Zhao, Bo; Cao, Peng; Hu, Shan; Li, Fan; Kong, Kangle; Zu, Yukun.
Afiliação
  • Zhao B; Department of Thoracic Surgery, Tongji Hospital, Huazhong University of Science and Technology Wuhan 430030, China.
  • Cao P; Department of Thoracic Surgery, Tongji Hospital, Huazhong University of Science and Technology Wuhan 430030, China.
  • Hu S; Department of Thoracic Surgery, Tongji Hospital, Huazhong University of Science and Technology Wuhan 430030, China.
  • Li F; Department of Thoracic Surgery, Tongji Hospital, Huazhong University of Science and Technology Wuhan 430030, China.
  • Kong K; Department of Thoracic Surgery, Tongji Hospital, Huazhong University of Science and Technology Wuhan 430030, China.
  • Zu Y; Department of Thoracic Surgery, Tongji Hospital, Huazhong University of Science and Technology Wuhan 430030, China.
Am J Transl Res ; 11(9): 5978-5987, 2019.
Article em En | MEDLINE | ID: mdl-31632565
Esophageal cancer is one of the most common malignant cancers worldwide. Long non-coding RNAs (lncRNAs) have been reported to be associated with different types of cancer; however, the precise function of lncRNAs in tumorigenesis remains largely unknown. Herein, we found that lncRNA NBAT-1 levels were lower in EC clinic tissues than in normal samples, and lncRNA NBAT-1 expression was negatively associated with prognosis and TNM stage in EC patients. More importantly, in EC cancer cells, lncRNA NBAT-1 overexpression strongly inhibited cell proliferation, cell growth and tumor glycolysis. Furthermore, a series of rescue experiments were performed to demonstrate that the role of lncRNA NBAT-1 in EC cell proliferation, cell growth and tumor glycolysis was partially dependent on the PKM2 protein, which is a key metabolic enzyme in tumor development. Taken together, our data illustrate a functional role for lncRNA NBAT-1 in metabolic reprogramming in EC cancer; thus, lncRNA NBAT-1 might be a potential clinical therapeutic target in EC patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article