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miR-26 Induces Apoptosis and Inhibits Autophagy in Non-small Cell Lung Cancer Cells by Suppressing TGF-ß1-JNK Signaling Pathway.
He, Yi; Liu, Hao; Jiang, Lianyong; Rui, Bi; Mei, Ju; Xiao, Haibo.
Afiliación
  • He Y; Department of Cardiothoracic Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Liu H; Department of Cardiothoracic Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Jiang L; Department of Cardiothoracic Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Rui B; Department of Cardiothoracic Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Mei J; Department of Cardiothoracic Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, China.
  • Xiao H; Department of Cardiothoracic Surgery, School of Medicine, Xinhua Hospital, Shanghai Jiao Tong University, Shanghai, China.
Front Pharmacol ; 9: 1509, 2018.
Article en En | MEDLINE | ID: mdl-30687089
Non-small cell lung cancer (NSCLC) is one of the causes of cancer mortality worldwide. The role of miR-26 in the development and progression of NSCLC remains largely unknown. In this study we found an abnormal expression of miR-26 in human NSCLC tissues. It was found that miR-26 mimics induced cell apoptosis and promoted caspase-3, 9 activities in human NSCLC cells. The miR-26 inhibitor enhanced the expression of the light chain 3 (LC3) protein and the autophagy related genes in NSCLC cells. Moreover, miR-26 regulated apoptosis and autophagy by inhibiting TGF-ß expression in a JNK dependent manner. In addition, miR-26 mimics induced cell apoptosis, was involved in the endoplasmic reticulum stress (ERS) signaling pathway. Down-regulation of the ERS, inhibited apoptosis which was induced by miR-26 mimics in NSCLC cells. In in vivo studies, TUNEL staining revealed that the number of TUNEL positive cells of the tumor tissue in the miR-26 treatment group, were significantly increased in comparison with the control group, while the number of TUNEL positive cells in the tumor tissue were remarkably decreased in the groups treated with miR-26, combined with the TGF-ß1 inhibitor or JNK inhibitor. Additionally, the immunoreactivity of TGF-ß1 in the cells treated with the miR-26 inhibitor, decreased in comparison to the control group. Our results indicated that miR-26 induced apoptosis and inhibited autophagy in human NSCLC cells through the TGF-ß1-JNK signaling pathway, suggesting that miR-26 could be a potential novel target for the treatment of NSCLC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Pharmacol Año: 2018 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Pharmacol Año: 2018 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza