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Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer
Gastric cancer (GC) is a multistep and multistage disease and the majority of GC cells could overexpressed one or more oncogenes. Trop2 and amphiregulin (AREG) are both overexpressed in various epithelial cell cancers and have the role in the increases tumor cells division and metastasis. However, l...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430091/ https://www.ncbi.nlm.nih.gov/pubmed/28256068 http://dx.doi.org/10.1002/cam4.1018 |
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author | Zhao, Wei Ding, Guipeng Wen, Jinbo Tang, Qi Yong, Hongmei Zhu, Huijun Zhang, Shu Qiu, Zhenning Feng, Zhenqing Zhu, Jin |
author_facet | Zhao, Wei Ding, Guipeng Wen, Jinbo Tang, Qi Yong, Hongmei Zhu, Huijun Zhang, Shu Qiu, Zhenning Feng, Zhenqing Zhu, Jin |
author_sort | Zhao, Wei |
collection | PubMed |
description | Gastric cancer (GC) is a multistep and multistage disease and the majority of GC cells could overexpressed one or more oncogenes. Trop2 and amphiregulin (AREG) are both overexpressed in various epithelial cell cancers and have the role in the increases tumor cells division and metastasis. However, little is known about the function and correlation of two oncogenes coexpressed in GC. The expression level of these two genes in 791 cases of GC tissues were tested, the correlations between two genes expression and clinical pathological characteristics and overall survival in GC patients through immunohistochemistry (IHC) were analyzed. This study also explored the mRNA expression level of two genes in 26 cases of freshly GC tissues by qRT‐PCR. The results indicated that Trop2+/AREG+ coexpression was higher in GC tissues than in adjacent tissues. Trop2+/AREG+ protein coexpression were associated with Tumor Node Metastasis (TNM) stage (χ (2) = 50.345, P < 0.001), tumor size (χ (2) = 40.349, P < 0.001), lymph node metastases (χ (2) = 26.481, P < 0.001), and distant metastases (χ (2) = 8.387, P = 0.039). GC patients with Trop2+ and AREG+ protein coexpression had poor overall survival rates (HR = 3.682, 95% CI = 2.038–6.654, P < 0.001). The expression level of Trop2/AREG were positively correlated (r 0.254 and P < 0.001). The result of the mRNA expression was similar to that of the protein expression. Overall, Trop2 and AREG could be seen as prognostic cobiomarker in GC and combined detection of Trop2 and AREG could be viewed as helpful in predicting the prognosis of the GC patients. |
format | Online Article Text |
id | pubmed-5430091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54300912017-05-17 Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer Zhao, Wei Ding, Guipeng Wen, Jinbo Tang, Qi Yong, Hongmei Zhu, Huijun Zhang, Shu Qiu, Zhenning Feng, Zhenqing Zhu, Jin Cancer Med Clinical Cancer Research Gastric cancer (GC) is a multistep and multistage disease and the majority of GC cells could overexpressed one or more oncogenes. Trop2 and amphiregulin (AREG) are both overexpressed in various epithelial cell cancers and have the role in the increases tumor cells division and metastasis. However, little is known about the function and correlation of two oncogenes coexpressed in GC. The expression level of these two genes in 791 cases of GC tissues were tested, the correlations between two genes expression and clinical pathological characteristics and overall survival in GC patients through immunohistochemistry (IHC) were analyzed. This study also explored the mRNA expression level of two genes in 26 cases of freshly GC tissues by qRT‐PCR. The results indicated that Trop2+/AREG+ coexpression was higher in GC tissues than in adjacent tissues. Trop2+/AREG+ protein coexpression were associated with Tumor Node Metastasis (TNM) stage (χ (2) = 50.345, P < 0.001), tumor size (χ (2) = 40.349, P < 0.001), lymph node metastases (χ (2) = 26.481, P < 0.001), and distant metastases (χ (2) = 8.387, P = 0.039). GC patients with Trop2+ and AREG+ protein coexpression had poor overall survival rates (HR = 3.682, 95% CI = 2.038–6.654, P < 0.001). The expression level of Trop2/AREG were positively correlated (r 0.254 and P < 0.001). The result of the mRNA expression was similar to that of the protein expression. Overall, Trop2 and AREG could be seen as prognostic cobiomarker in GC and combined detection of Trop2 and AREG could be viewed as helpful in predicting the prognosis of the GC patients. John Wiley and Sons Inc. 2017-03-03 /pmc/articles/PMC5430091/ /pubmed/28256068 http://dx.doi.org/10.1002/cam4.1018 Text en © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Cancer Research Zhao, Wei Ding, Guipeng Wen, Jinbo Tang, Qi Yong, Hongmei Zhu, Huijun Zhang, Shu Qiu, Zhenning Feng, Zhenqing Zhu, Jin Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer |
title | Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer |
title_full | Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer |
title_fullStr | Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer |
title_full_unstemmed | Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer |
title_short | Correlation between Trop2 and amphiregulin coexpression and overall survival in gastric cancer |
title_sort | correlation between trop2 and amphiregulin coexpression and overall survival in gastric cancer |
topic | Clinical Cancer Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5430091/ https://www.ncbi.nlm.nih.gov/pubmed/28256068 http://dx.doi.org/10.1002/cam4.1018 |
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