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Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis
A section of gastric cancers presents nuclear β-catenin accumulation correlated with H. pylori infection. H. pylori stimulate Wnt/β-catenin pathway by activating oncogenic c-Met and epidermal growth factor receptor (EGFR), or by inhibiting tumor suppressor Runx3 and Trefoil factor 1 (TFF1). H. pylor...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742126/ https://www.ncbi.nlm.nih.gov/pubmed/26417932 |
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author | Song, Xiaowen Xin, Na Wang, Wei Zhao, Chenghai |
author_facet | Song, Xiaowen Xin, Na Wang, Wei Zhao, Chenghai |
author_sort | Song, Xiaowen |
collection | PubMed |
description | A section of gastric cancers presents nuclear β-catenin accumulation correlated with H. pylori infection. H. pylori stimulate Wnt/β-catenin pathway by activating oncogenic c-Met and epidermal growth factor receptor (EGFR), or by inhibiting tumor suppressor Runx3 and Trefoil factor 1 (TFF1). H. pylori also trigger Wnt/β-catenin pathway by recruiting macrophages. Moreover, Wnt/β-catenin pathway is found involved in H. pylori-induced gastric cancer stem cell generation. Recently, by using gastroids, researchers have further revealed that H. pylori induce gastric epithelial cell proliferation through β-catenin. These findings indicate that Wnt/β-catenin is an oncogenic pathway activated by H. pylori. Therefore, this pathway is a potential therapy target for H. pylori-related gastric cancer. |
format | Online Article Text |
id | pubmed-4742126 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-47421262016-04-04 Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis Song, Xiaowen Xin, Na Wang, Wei Zhao, Chenghai Oncotarget Review A section of gastric cancers presents nuclear β-catenin accumulation correlated with H. pylori infection. H. pylori stimulate Wnt/β-catenin pathway by activating oncogenic c-Met and epidermal growth factor receptor (EGFR), or by inhibiting tumor suppressor Runx3 and Trefoil factor 1 (TFF1). H. pylori also trigger Wnt/β-catenin pathway by recruiting macrophages. Moreover, Wnt/β-catenin pathway is found involved in H. pylori-induced gastric cancer stem cell generation. Recently, by using gastroids, researchers have further revealed that H. pylori induce gastric epithelial cell proliferation through β-catenin. These findings indicate that Wnt/β-catenin is an oncogenic pathway activated by H. pylori. Therefore, this pathway is a potential therapy target for H. pylori-related gastric cancer. Impact Journals LLC 2015-09-21 /pmc/articles/PMC4742126/ /pubmed/26417932 Text en Copyright: © 2015 Song et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Review Song, Xiaowen Xin, Na Wang, Wei Zhao, Chenghai Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis |
title | Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis |
title_full | Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis |
title_fullStr | Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis |
title_full_unstemmed | Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis |
title_short | Wnt/β-catenin, an oncogenic pathway targeted by H. pylori in gastric carcinogenesis |
title_sort | wnt/β-catenin, an oncogenic pathway targeted by h. pylori in gastric carcinogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4742126/ https://www.ncbi.nlm.nih.gov/pubmed/26417932 |
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