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Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review

BACKGROUND: The special AT-rich sequence-binding proteins 1 (SATB1) is a major regulator involved in cell differentiation. It has been shown that SATB1 acts as an oncogenic regulator. The clinical and prognostic significance of SATB1 in gastrointestinal cancer remains controversial. The purpose of t...

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Autores principales: Zhang, Sheng, Tong, Yi Xin, Xu, Xiang Shang, Lin, Hui, Chao, Teng Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564658/
https://www.ncbi.nlm.nih.gov/pubmed/28430598
http://dx.doi.org/10.18632/oncotarget.16867
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author Zhang, Sheng
Tong, Yi Xin
Xu, Xiang Shang
Lin, Hui
Chao, Teng Fei
author_facet Zhang, Sheng
Tong, Yi Xin
Xu, Xiang Shang
Lin, Hui
Chao, Teng Fei
author_sort Zhang, Sheng
collection PubMed
description BACKGROUND: The special AT-rich sequence-binding proteins 1 (SATB1) is a major regulator involved in cell differentiation. It has been shown that SATB1 acts as an oncogenic regulator. The clinical and prognostic significance of SATB1 in gastrointestinal cancer remains controversial. The purpose of this study is to conduct a systematic review and meta-analysis to elucidate the impact of SATB1 in gastrointestinal cancer. RESULTS: A total of 3174 gastrointestinal cancer patients from 15 studies were included. The correlation between SATB1 expression and OS or RFS was investigated in 12 and 5 studies respectively. The results of meta-analysis showed that SATB1 overexpression is inversely correlated with OS (combined HR: 1.79, p = 0.0003) and RFS (combined HR: 2.46, p < 0.0001). In subgroup analysis, SATB1 expression is significantly correlated with poor prognosis in gastrointestinal cancer in Asian population. SATB1 expression is associated with stage, invasion depth, lymph node metastasis and distant metastasis. METHODOLOGY: Published studies with data on overall survival (OS) and/or relapse free survival (RFS) and SATB1 expression were searched from Cochrane Library, PubMed and Embase (up to Dec 30, 2016). The outcome measurement is hazard ratio (HR) for OS or RFS related with SATB1 expression. Two reviewers independently screened the literatures, extracted the data and performed meta-analysis using RevMan 5.3.0 software. The combined HRs were calculated by fixed- or random-effect models. CONCLUSIONS: The results of this meta-analysis suggest that SATB1 overexpression is related to advanced stage, lymph node metastasis and distant metastasis. SATB1 overexpression is a marker indicating poor prognosis in gastrointestinal cancer.
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spelling pubmed-55646582017-08-23 Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review Zhang, Sheng Tong, Yi Xin Xu, Xiang Shang Lin, Hui Chao, Teng Fei Oncotarget Review BACKGROUND: The special AT-rich sequence-binding proteins 1 (SATB1) is a major regulator involved in cell differentiation. It has been shown that SATB1 acts as an oncogenic regulator. The clinical and prognostic significance of SATB1 in gastrointestinal cancer remains controversial. The purpose of this study is to conduct a systematic review and meta-analysis to elucidate the impact of SATB1 in gastrointestinal cancer. RESULTS: A total of 3174 gastrointestinal cancer patients from 15 studies were included. The correlation between SATB1 expression and OS or RFS was investigated in 12 and 5 studies respectively. The results of meta-analysis showed that SATB1 overexpression is inversely correlated with OS (combined HR: 1.79, p = 0.0003) and RFS (combined HR: 2.46, p < 0.0001). In subgroup analysis, SATB1 expression is significantly correlated with poor prognosis in gastrointestinal cancer in Asian population. SATB1 expression is associated with stage, invasion depth, lymph node metastasis and distant metastasis. METHODOLOGY: Published studies with data on overall survival (OS) and/or relapse free survival (RFS) and SATB1 expression were searched from Cochrane Library, PubMed and Embase (up to Dec 30, 2016). The outcome measurement is hazard ratio (HR) for OS or RFS related with SATB1 expression. Two reviewers independently screened the literatures, extracted the data and performed meta-analysis using RevMan 5.3.0 software. The combined HRs were calculated by fixed- or random-effect models. CONCLUSIONS: The results of this meta-analysis suggest that SATB1 overexpression is related to advanced stage, lymph node metastasis and distant metastasis. SATB1 overexpression is a marker indicating poor prognosis in gastrointestinal cancer. Impact Journals LLC 2017-04-05 /pmc/articles/PMC5564658/ /pubmed/28430598 http://dx.doi.org/10.18632/oncotarget.16867 Text en Copyright: © 2017 Zhang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (http://creativecommons.org/licenses/by/3.0/) (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Review
Zhang, Sheng
Tong, Yi Xin
Xu, Xiang Shang
Lin, Hui
Chao, Teng Fei
Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review
title Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review
title_full Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review
title_fullStr Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review
title_full_unstemmed Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review
title_short Prognostic significance of SATB1 in gastrointestinal cancer: a meta-analysis and literature review
title_sort prognostic significance of satb1 in gastrointestinal cancer: a meta-analysis and literature review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5564658/
https://www.ncbi.nlm.nih.gov/pubmed/28430598
http://dx.doi.org/10.18632/oncotarget.16867
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