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High SPRR1A expression is associated with poor survival in patients with colon cancer
High expression of small proline-rich protein 1A (SPRR1A) has been shown to be associated with tumor prognosis; however, the association between SPRR1A expression and colon cancer prognosis remains unclear. The present study sought to evaluate the association between SPRR1A expression and the clinic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115157/ https://www.ncbi.nlm.nih.gov/pubmed/32269614 http://dx.doi.org/10.3892/ol.2020.11453 |
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author | Deng, Yu Zheng, Xin Zhang, Yiyi Xu, Meifang Ye, Chengwei Lin, Mengxin Pan, Jie Xu, Zongbin Lu, Xingrong Chi, Pan |
author_facet | Deng, Yu Zheng, Xin Zhang, Yiyi Xu, Meifang Ye, Chengwei Lin, Mengxin Pan, Jie Xu, Zongbin Lu, Xingrong Chi, Pan |
author_sort | Deng, Yu |
collection | PubMed |
description | High expression of small proline-rich protein 1A (SPRR1A) has been shown to be associated with tumor prognosis; however, the association between SPRR1A expression and colon cancer prognosis remains unclear. The present study sought to evaluate the association between SPRR1A expression and the clinicopathological characteristics of colon cancer, and to examine its potential prognostic value. A total of 114 patients with colon cancer were included. SPRR1A expression was evaluated by immunohistochemical staining, and the association between SPRR1A expression and clinicopathological parameters was analyzed. The prognostic value of SPRR1A was analyzed by Cox regression analysis, the Oncomine database and the R2 platform. SPRR1A expression was significantly increased in cancerous tissues compared with that in adjacent non-cancerous tissues. SPPRR1A expression was significantly associated with lymph node invasion. High SPRR1A expression was significantly associated with worse overall and disease-free survival rate. Cox regression analysis revealed that T stage, pathological N stage and high SPRR1A expression remained independent predictors for overall survival rate. The Oncomine database analysis demonstrated that SPRR1A mRNA expression levels were significantly increased in colorectal cancer tissues compared with those in adjacent non-cancerous tissues, and high SPRR1A expression was associated with a significantly worse event- and relapse-free survival time in the R2 platform. The data indicate that SPRR1A may serve as a potential biomarker for the prognosis of colon cancer. |
format | Online Article Text |
id | pubmed-7115157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-71151572020-04-08 High SPRR1A expression is associated with poor survival in patients with colon cancer Deng, Yu Zheng, Xin Zhang, Yiyi Xu, Meifang Ye, Chengwei Lin, Mengxin Pan, Jie Xu, Zongbin Lu, Xingrong Chi, Pan Oncol Lett Articles High expression of small proline-rich protein 1A (SPRR1A) has been shown to be associated with tumor prognosis; however, the association between SPRR1A expression and colon cancer prognosis remains unclear. The present study sought to evaluate the association between SPRR1A expression and the clinicopathological characteristics of colon cancer, and to examine its potential prognostic value. A total of 114 patients with colon cancer were included. SPRR1A expression was evaluated by immunohistochemical staining, and the association between SPRR1A expression and clinicopathological parameters was analyzed. The prognostic value of SPRR1A was analyzed by Cox regression analysis, the Oncomine database and the R2 platform. SPRR1A expression was significantly increased in cancerous tissues compared with that in adjacent non-cancerous tissues. SPPRR1A expression was significantly associated with lymph node invasion. High SPRR1A expression was significantly associated with worse overall and disease-free survival rate. Cox regression analysis revealed that T stage, pathological N stage and high SPRR1A expression remained independent predictors for overall survival rate. The Oncomine database analysis demonstrated that SPRR1A mRNA expression levels were significantly increased in colorectal cancer tissues compared with those in adjacent non-cancerous tissues, and high SPRR1A expression was associated with a significantly worse event- and relapse-free survival time in the R2 platform. The data indicate that SPRR1A may serve as a potential biomarker for the prognosis of colon cancer. D.A. Spandidos 2020-05 2020-03-10 /pmc/articles/PMC7115157/ /pubmed/32269614 http://dx.doi.org/10.3892/ol.2020.11453 Text en Copyright: © Deng et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Deng, Yu Zheng, Xin Zhang, Yiyi Xu, Meifang Ye, Chengwei Lin, Mengxin Pan, Jie Xu, Zongbin Lu, Xingrong Chi, Pan High SPRR1A expression is associated with poor survival in patients with colon cancer |
title | High SPRR1A expression is associated with poor survival in patients with colon cancer |
title_full | High SPRR1A expression is associated with poor survival in patients with colon cancer |
title_fullStr | High SPRR1A expression is associated with poor survival in patients with colon cancer |
title_full_unstemmed | High SPRR1A expression is associated with poor survival in patients with colon cancer |
title_short | High SPRR1A expression is associated with poor survival in patients with colon cancer |
title_sort | high sprr1a expression is associated with poor survival in patients with colon cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115157/ https://www.ncbi.nlm.nih.gov/pubmed/32269614 http://dx.doi.org/10.3892/ol.2020.11453 |
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