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Isoprenaline Induces Periostin Expression in Gastric Cancer
PURPOSE: Periostin mediates critical steps in gastric cancer and is involved in various signaling pathways. However, the roles of periostin in promoting gastric cancer metastasis are not clear. The aim of this study was to investigate the relevance between periostin expression and gastric cancer pro...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Yonsei University College of Medicine
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800342/ https://www.ncbi.nlm.nih.gov/pubmed/26996552 http://dx.doi.org/10.3349/ymj.2016.57.3.557 |
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author | Liu, Guo-Xiao Xi, Hong-Qing Sun, Xiao-Yan Geng, Zhi-Jun Yang, Shao-Wei Lu, Yan-Jie Wei, Bo Chen, Lin |
author_facet | Liu, Guo-Xiao Xi, Hong-Qing Sun, Xiao-Yan Geng, Zhi-Jun Yang, Shao-Wei Lu, Yan-Jie Wei, Bo Chen, Lin |
author_sort | Liu, Guo-Xiao |
collection | PubMed |
description | PURPOSE: Periostin mediates critical steps in gastric cancer and is involved in various signaling pathways. However, the roles of periostin in promoting gastric cancer metastasis are not clear. The aim of this study was to investigate the relevance between periostin expression and gastric cancer progression and the role of stress-related hormones in the regulation of cancer development and progression. MATERIALS AND METHODS: Normal, cancerous and metastatic gastric tissues were collected from patients diagnosed with advanced gastric cancer. The in vivo expression of periostin was evaluated by in situ hybridization and immunofluorescent staining. Meanwhile, human gastric adenocarcinoma cell lines MKN-45 and BGC-803 were used to detect the in vitro expression of periostin by using quantitative real-time polymerase chain reaction (PCR) and western blotting. RESULTS: Periostin is expressed in the stroma of the primary gastric tumors and metastases, but not in normal gastric tissue. In addition, we observed that periostin is located mainly in pericryptal fibroblasts, but not in the tumor cells, and strongly correlated to the expression of α-smooth muscle actin (SMA). Furthermore, the distribution patterns of periostin were broader as the clinical staging of tumors progressed. We also identified a role of stress-related signaling in promoting cancer development and progression, and found that isoprenaline upregulated expression levels of periostin in gastric cancer cells. CONCLUSION: These findings suggest that the distribution pattern of periostin was broader as the clinical staging of the tumor progressed and found that isoprenaline upregulated expression levels of periostin in gastric cancer cells. |
format | Online Article Text |
id | pubmed-4800342 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Yonsei University College of Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-48003422016-05-01 Isoprenaline Induces Periostin Expression in Gastric Cancer Liu, Guo-Xiao Xi, Hong-Qing Sun, Xiao-Yan Geng, Zhi-Jun Yang, Shao-Wei Lu, Yan-Jie Wei, Bo Chen, Lin Yonsei Med J Original Article PURPOSE: Periostin mediates critical steps in gastric cancer and is involved in various signaling pathways. However, the roles of periostin in promoting gastric cancer metastasis are not clear. The aim of this study was to investigate the relevance between periostin expression and gastric cancer progression and the role of stress-related hormones in the regulation of cancer development and progression. MATERIALS AND METHODS: Normal, cancerous and metastatic gastric tissues were collected from patients diagnosed with advanced gastric cancer. The in vivo expression of periostin was evaluated by in situ hybridization and immunofluorescent staining. Meanwhile, human gastric adenocarcinoma cell lines MKN-45 and BGC-803 were used to detect the in vitro expression of periostin by using quantitative real-time polymerase chain reaction (PCR) and western blotting. RESULTS: Periostin is expressed in the stroma of the primary gastric tumors and metastases, but not in normal gastric tissue. In addition, we observed that periostin is located mainly in pericryptal fibroblasts, but not in the tumor cells, and strongly correlated to the expression of α-smooth muscle actin (SMA). Furthermore, the distribution patterns of periostin were broader as the clinical staging of tumors progressed. We also identified a role of stress-related signaling in promoting cancer development and progression, and found that isoprenaline upregulated expression levels of periostin in gastric cancer cells. CONCLUSION: These findings suggest that the distribution pattern of periostin was broader as the clinical staging of the tumor progressed and found that isoprenaline upregulated expression levels of periostin in gastric cancer cells. Yonsei University College of Medicine 2016-05-01 2016-03-15 /pmc/articles/PMC4800342/ /pubmed/26996552 http://dx.doi.org/10.3349/ymj.2016.57.3.557 Text en © Copyright: Yonsei University College of Medicine 2016 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Liu, Guo-Xiao Xi, Hong-Qing Sun, Xiao-Yan Geng, Zhi-Jun Yang, Shao-Wei Lu, Yan-Jie Wei, Bo Chen, Lin Isoprenaline Induces Periostin Expression in Gastric Cancer |
title | Isoprenaline Induces Periostin Expression in Gastric Cancer |
title_full | Isoprenaline Induces Periostin Expression in Gastric Cancer |
title_fullStr | Isoprenaline Induces Periostin Expression in Gastric Cancer |
title_full_unstemmed | Isoprenaline Induces Periostin Expression in Gastric Cancer |
title_short | Isoprenaline Induces Periostin Expression in Gastric Cancer |
title_sort | isoprenaline induces periostin expression in gastric cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800342/ https://www.ncbi.nlm.nih.gov/pubmed/26996552 http://dx.doi.org/10.3349/ymj.2016.57.3.557 |
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