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10.1097/MD.0000000000008166

http://scihub22266oqcxt.onion/10.1097/MD.0000000000008166
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suck abstract from ncbi


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pmid29068985
      Medicine+(Baltimore) 2017 ; 96 (43 ): e8166
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  • Effects of TRPC1 on epithelial mesenchymal transition in human airway in chronic obstructive pulmonary disease #MMPMID29068985
  • Xu F ; Liu XC ; Li L ; Ma CN ; Zhang YJ
  • Medicine (Baltimore) 2017[Oct]; 96 (43 ): e8166 PMID29068985 show ga
  • BACKGROUND: We investigated the effects of TRPC1 on epithelial mesenchymal transition (EMT) in human airway in chronic obstructive pulmonary disease (COPD). METHODS: A total of 94 patients who underwent lobectomy were selected and divided into COPD (49 cases) and control (45 cases) groups. Immunohistochemistry was applied to detect expression of E-cadherin and vimentin and TRPC1. Correlation of TRPC1 expression with E-cadherin and vimentin expression, and correlations of lung function indicators in COPD patients with expression of TRPC1, E-cadherin, and vimentin were analyzed. Human airway epithelial cells (16HBE) were used for cell experiments; and cigarette smoking extract (CSE) was adopted to establish the COPD model using TRPC1 recombinant plasmids and siRNA. Cells were assigned into the control, CSE, CSE?+?vector, CSE?+?TRPC1, CSE?+?si-NC, and CSE?+?si-TRPC1 groups. Quantitative real-time polymerase chain reaction (qRT-PCR) and Western blot were implemented to detect expression of TRPC1, E-cadherin, and vimentin. RESULTS: Compared with the control group, expression of TRPC1 and vimentin significantly increased while expression of E-cadherin decreased in the COPD group, and protein expression of TRPC1 was positively correlated with the protein expression of vimentin but negatively correlated with the protein expression of E-cadherin. Patients exhibiting positive expression of TRPC1 had lower FEV1, FEV1%Pred, and FEV1/FVC, compared with the patients exhibiting negative expression of TRPC1. Compared with the control group, expression of TRPC1 and vimentin increased, whereas expression of E-cadherin decreased in the CSE, CSE?+?vector, CSE?+?TRPC1, and CSE?+?si-NC groups. Compared with the CSE and CSE?+?vector groups, the expression of TRPC1 and vimentin increased but the expression of E-cadherin decreased in the CSE?+?TRPC1 group. Compared with the CSE and CSE?+?si-NC groups, the expression of TRPC1 and vimentin decreased but the expression of E-cadherin increased in the CSE?+?si-TRPC1 group. No significant differences were observed among the CSE, CSE?+?vector and CSE?+?si-NC groups. CONCLUSION: Overexpression of TRPC1 in COPD promoted EMT process and TRPC1 may be a new and interesting focus for COPD new treatment in the future.
  • |*Epithelial-Mesenchymal Transition [MESH]
  • |Adult [MESH]
  • |Aged [MESH]
  • |Blotting, Western [MESH]
  • |Cadherins/metabolism [MESH]
  • |Cells, Cultured [MESH]
  • |Epithelial Cells/metabolism [MESH]
  • |Female [MESH]
  • |Humans [MESH]
  • |Immunohistochemistry [MESH]
  • |Lung/metabolism/pathology/physiopathology [MESH]
  • |Male [MESH]
  • |Middle Aged [MESH]
  • |Pulmonary Disease, Chronic Obstructive/*metabolism/*pathology/physiopathology [MESH]
  • |Real-Time Polymerase Chain Reaction [MESH]
  • |TRPC Cation Channels/*metabolism [MESH]


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