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THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer

Colorectal cancer is one of the most common leading causes of death worldwide. Prognostic at an early stage is a useful way that decrease and avoid mortality. Although remarkable progress has been made to investigate the underlying mechanism, the understanding of the complicated carcinogenesis proce...

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Autores principales: Wang, Xue, Zhang, Lei, Li, Hui, Sun, WenJie, Zhang, Honghe, Lai, Maode
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025892/
https://www.ncbi.nlm.nih.gov/pubmed/27632935
http://dx.doi.org/10.1038/srep33366
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author Wang, Xue
Zhang, Lei
Li, Hui
Sun, WenJie
Zhang, Honghe
Lai, Maode
author_facet Wang, Xue
Zhang, Lei
Li, Hui
Sun, WenJie
Zhang, Honghe
Lai, Maode
author_sort Wang, Xue
collection PubMed
description Colorectal cancer is one of the most common leading causes of death worldwide. Prognostic at an early stage is a useful way that decrease and avoid mortality. Although remarkable progress has been made to investigate the underlying mechanism, the understanding of the complicated carcinogenesis process was enormously hindered by large-scale tumor heterogeneity. Here we proposed that the prognosis-related gene THBS2, responsible for cooperativity disorientation, probably contain untapped prognostic resource of colorectal cancer. We originally established Spearman correlation transition, Kaplan–Meier survival analysis and meta-analysis that combine public dataset and clinical samples to quantify the prognostic value of THBS2. THBS2 could be considered as a novel prognostic marker in colorectal cancer.
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spelling pubmed-50258922016-09-22 THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer Wang, Xue Zhang, Lei Li, Hui Sun, WenJie Zhang, Honghe Lai, Maode Sci Rep Article Colorectal cancer is one of the most common leading causes of death worldwide. Prognostic at an early stage is a useful way that decrease and avoid mortality. Although remarkable progress has been made to investigate the underlying mechanism, the understanding of the complicated carcinogenesis process was enormously hindered by large-scale tumor heterogeneity. Here we proposed that the prognosis-related gene THBS2, responsible for cooperativity disorientation, probably contain untapped prognostic resource of colorectal cancer. We originally established Spearman correlation transition, Kaplan–Meier survival analysis and meta-analysis that combine public dataset and clinical samples to quantify the prognostic value of THBS2. THBS2 could be considered as a novel prognostic marker in colorectal cancer. Nature Publishing Group 2016-09-16 /pmc/articles/PMC5025892/ /pubmed/27632935 http://dx.doi.org/10.1038/srep33366 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Wang, Xue
Zhang, Lei
Li, Hui
Sun, WenJie
Zhang, Honghe
Lai, Maode
THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer
title THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer
title_full THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer
title_fullStr THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer
title_full_unstemmed THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer
title_short THBS2 is a Potential Prognostic Biomarker in Colorectal Cancer
title_sort thbs2 is a potential prognostic biomarker in colorectal cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025892/
https://www.ncbi.nlm.nih.gov/pubmed/27632935
http://dx.doi.org/10.1038/srep33366
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