Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue
Background/Aims Epithelial-mesenchymal transition (EMT) is a developmental process, wherein the epithelial cells show reduced intercellular adhesions and acquire migratory fibroblastic properties. EMT is associated with downregulation in epithelial marker expression, abnormal translocation of E-cadh...
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Hoon Jai Chun
2019-09-01
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doaj-cbebaf87188840efb1cf2503f0e45de62020-11-24T21:47:52ZengHoon Jai ChunClinical Endoscopy2234-24002234-24432019-09-0152546447110.5946/ce.2018.1817219Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer TissueHee Jae Jung0Su Jin Hong1Shin Hee Kim2 Digestive Disease Center and Research Institute, Soonchunhyang University College of Medicine, Bucheon, Korea Digestive Disease Center and Research Institute, Soonchunhyang University College of Medicine, Bucheon, Korea Digestive Disease Center and Research Institute, Soonchunhyang University College of Medicine, Bucheon, KoreaBackground/Aims Epithelial-mesenchymal transition (EMT) is a developmental process, wherein the epithelial cells show reduced intercellular adhesions and acquire migratory fibroblastic properties. EMT is associated with downregulation in epithelial marker expression, abnormal translocation of E-cadherin, and upregulation in mesenchymal marker expression. Here, we investigated the immunohistochemical (IHC) expression of EMT markers in early gastric cancer (EGC) between cancer and noncancer tissues. Methods Tissue samples were prospectively obtained from 19 patients with EGC that underwent endoscopic submucosal dissection (ESD). We compared the expression level of transforming growth factor (TGF)-β, vascular endothelial growth factor (VEGF), E-cadherin, α-smooth muscle actin (α-SMA), and vimentin between cancer and noncancer tissues using IHC. Among the 19 patients, 15 patients had follow-up biopsy at 3 months after ESD for EGC. Results Cancer tissues presented higher values of EMT mesenchymal markers (α-SMA/vimentin/TGF-β/VEGF) than the noncancerous tissues (p<0.05) that were significantly low after ESD (p<0.05). No significant correlation was reported for tumor location and initial Helicobacter pylori infection. Conclusions The mesenchymal expression of EMT markers was higher in the cancerous tissues than in the noncancer tissues.http://www.e-ce.org/upload/pdf/ce-2018-181.pdfEpithelial-mesenchymal transitionImmunohistochemistryEarly gastric cancerEndoscopic submucosal dissection |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Hee Jae Jung Su Jin Hong Shin Hee Kim |
spellingShingle |
Hee Jae Jung Su Jin Hong Shin Hee Kim Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue Clinical Endoscopy Epithelial-mesenchymal transition Immunohistochemistry Early gastric cancer Endoscopic submucosal dissection |
author_facet |
Hee Jae Jung Su Jin Hong Shin Hee Kim |
author_sort |
Hee Jae Jung |
title |
Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue |
title_short |
Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue |
title_full |
Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue |
title_fullStr |
Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue |
title_full_unstemmed |
Immunohistochemical Expression of Epithelial-Mesenchymal Transition Markers in Early Gastric Cancer: Cancer Tissue versus Noncancer Tissue |
title_sort |
immunohistochemical expression of epithelial-mesenchymal transition markers in early gastric cancer: cancer tissue versus noncancer tissue |
publisher |
Hoon Jai Chun |
series |
Clinical Endoscopy |
issn |
2234-2400 2234-2443 |
publishDate |
2019-09-01 |
description |
Background/Aims Epithelial-mesenchymal transition (EMT) is a developmental process, wherein the epithelial cells show reduced intercellular adhesions and acquire migratory fibroblastic properties. EMT is associated with downregulation in epithelial marker expression, abnormal translocation of E-cadherin, and upregulation in mesenchymal marker expression. Here, we investigated the immunohistochemical (IHC) expression of EMT markers in early gastric cancer (EGC) between cancer and noncancer tissues. Methods Tissue samples were prospectively obtained from 19 patients with EGC that underwent endoscopic submucosal dissection (ESD). We compared the expression level of transforming growth factor (TGF)-β, vascular endothelial growth factor (VEGF), E-cadherin, α-smooth muscle actin (α-SMA), and vimentin between cancer and noncancer tissues using IHC. Among the 19 patients, 15 patients had follow-up biopsy at 3 months after ESD for EGC. Results Cancer tissues presented higher values of EMT mesenchymal markers (α-SMA/vimentin/TGF-β/VEGF) than the noncancerous tissues (p<0.05) that were significantly low after ESD (p<0.05). No significant correlation was reported for tumor location and initial Helicobacter pylori infection. Conclusions The mesenchymal expression of EMT markers was higher in the cancerous tissues than in the noncancer tissues. |
topic |
Epithelial-mesenchymal transition Immunohistochemistry Early gastric cancer Endoscopic submucosal dissection |
url |
http://www.e-ce.org/upload/pdf/ce-2018-181.pdf |
work_keys_str_mv |
AT heejaejung immunohistochemicalexpressionofepithelialmesenchymaltransitionmarkersinearlygastriccancercancertissueversusnoncancertissue AT sujinhong immunohistochemicalexpressionofepithelialmesenchymaltransitionmarkersinearlygastriccancercancertissueversusnoncancertissue AT shinheekim immunohistochemicalexpressionofepithelialmesenchymaltransitionmarkersinearlygastriccancercancertissueversusnoncancertissue |
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