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CFTR activation suppresses glioblastoma cell proliferation, migration and invasion.
Zhong, Xiao; Chen, Hong-Qi; Yang, Xiu-Ling; Wang, Qing; Chen, Wenliang; Li, Chunfu.
Afiliación
  • Zhong X; Department of Paediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Chen HQ; Department of Pharmacology, Guangzhou Medical University, Guangzhou, China.
  • Yang XL; Department of Paediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Wang Q; Department of Paediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China.
  • Chen W; Department of Pharmacology, Guangzhou Medical University, Guangzhou, China. Electronic address: wenliang.chen@utoronto.ca.
  • Li C; Department of Paediatrics, Nanfang Hospital, Southern Medical University, Guangzhou, China. Electronic address: chunfugzcn@126.com.
Biochem Biophys Res Commun ; 508(4): 1279-1285, 2019 01 22.
Article en En | MEDLINE | ID: mdl-30573361
ABSTRACT
The aim of this study was to investigate the function of Cystic fibrosis transmembrane conductance regulator (CFTR) in human glioblastoma (GBM) cells. Data dining results of the Human Protein Atlas showed that low CFTR expression was associated with poor prognosis for GBM patients. We found that CFTR protein expression was lower in U87 and U251 GBM cells than that in normal humane astrocyte cells. CFTR activation significantly reduced GBM cell proliferation. In addition, CFTR activation significantly abrogated migration and invasion of GBM cells. Besides, CFTR activator Forskolin treatment markedly reduced MMP-2 protein expression. These effects of CFTR activation were significantly inhibited by CFTR inhibitor CFTRinh-172 pretreatment. Our findings suggested that JAK2/STAT3 signaling was involved in the anti-glioblastoma effects of CFTR activation. Moreover, CFTR overexpression in combination with Forskolin induced a synergistic anti-proliferative response in U87 cells. Overall, our findings demonstrated that CFTR activation suppressed GBM cell proliferation, migration and invasion likely through the inhibition of JAK2/STAT3 signaling.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Movimiento Celular / Glioblastoma / Regulador de Conductancia de Transmembrana de Fibrosis Quística Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2019 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Movimiento Celular / Glioblastoma / Regulador de Conductancia de Transmembrana de Fibrosis Quística Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Biochem Biophys Res Commun Año: 2019 Tipo del documento: Article País de afiliación: China