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Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis
INTRODUCTION: SEMA4D and its high affinity receptor Plexin-B1 showed a promising prognosis prediction for carcinoma patients in recent studies, we performed a meta-analysis to evaluate the prognostic role of them in various malignancies. METHODS: A systematic literature search was performed in PubMe...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407964/ https://www.ncbi.nlm.nih.gov/pubmed/30762724 http://dx.doi.org/10.1097/MD.0000000000013298 |
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author | Yang, Yibo Wang, Jing Li, Hui Liu, Lihong Yao, Maojin Xiao, Tao |
author_facet | Yang, Yibo Wang, Jing Li, Hui Liu, Lihong Yao, Maojin Xiao, Tao |
author_sort | Yang, Yibo |
collection | PubMed |
description | INTRODUCTION: SEMA4D and its high affinity receptor Plexin-B1 showed a promising prognosis prediction for carcinoma patients in recent studies, we performed a meta-analysis to evaluate the prognostic role of them in various malignancies. METHODS: A systematic literature search was performed in PubMed, Embase, Web of Science, and CNKI from inception till July 2017. Eligible studies were identified by different reviewers. Hazard ratios (HRs)/related ratios (RRs) and their corresponding 95% confidence intervals (CIs) were extracted to investigate the relevance between malignancies prognosis and SEMA4D/Plexin-B1. RESULTS: Around 2638 patients from 14 studies were included in this meta-analysis. High expression of SEMA4D was significantly associated with overall survival (OS) and disease-free survival/progression-free survival/recurrence-free survival (DFS/PFS/RFS) in tumors (respectively, HR(os) = 2.05, 95%CI: 1.68–2.50, P < .001; HR(dfs/pfs/rfs) = 1.59, 95%CI = 1.27–1.98, P < .001). However, the relationship between SEMA4D expression and prognosis of breast cancer patients was failed to find (HR = 0.76, 95%CI = 0.32–1.82, P = .539). Plexin-B1 level showed a significant positive correlation both with OS and DFS of Caucasian breast cancer patients (respectively, HR(os) = 0.56, 95%CI: 0.39–0.79, P = .001; HR(dfs) = 0.68, 95%CI = 0.51–0.90, P = .008) CONCLUSIONS: SEMA4D could be a prospective biomarker for prognostic prediction of various malignancies except breast cancer. For Caucasian breast cancer patients, SEMA4D's high affinity receptor Plexin-B1 showed a significant positive correlation with survival. |
format | Online Article Text |
id | pubmed-6407964 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-64079642019-03-16 Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis Yang, Yibo Wang, Jing Li, Hui Liu, Lihong Yao, Maojin Xiao, Tao Medicine (Baltimore) Research Article INTRODUCTION: SEMA4D and its high affinity receptor Plexin-B1 showed a promising prognosis prediction for carcinoma patients in recent studies, we performed a meta-analysis to evaluate the prognostic role of them in various malignancies. METHODS: A systematic literature search was performed in PubMed, Embase, Web of Science, and CNKI from inception till July 2017. Eligible studies were identified by different reviewers. Hazard ratios (HRs)/related ratios (RRs) and their corresponding 95% confidence intervals (CIs) were extracted to investigate the relevance between malignancies prognosis and SEMA4D/Plexin-B1. RESULTS: Around 2638 patients from 14 studies were included in this meta-analysis. High expression of SEMA4D was significantly associated with overall survival (OS) and disease-free survival/progression-free survival/recurrence-free survival (DFS/PFS/RFS) in tumors (respectively, HR(os) = 2.05, 95%CI: 1.68–2.50, P < .001; HR(dfs/pfs/rfs) = 1.59, 95%CI = 1.27–1.98, P < .001). However, the relationship between SEMA4D expression and prognosis of breast cancer patients was failed to find (HR = 0.76, 95%CI = 0.32–1.82, P = .539). Plexin-B1 level showed a significant positive correlation both with OS and DFS of Caucasian breast cancer patients (respectively, HR(os) = 0.56, 95%CI: 0.39–0.79, P = .001; HR(dfs) = 0.68, 95%CI = 0.51–0.90, P = .008) CONCLUSIONS: SEMA4D could be a prospective biomarker for prognostic prediction of various malignancies except breast cancer. For Caucasian breast cancer patients, SEMA4D's high affinity receptor Plexin-B1 showed a significant positive correlation with survival. Wolters Kluwer Health 2019-02-15 /pmc/articles/PMC6407964/ /pubmed/30762724 http://dx.doi.org/10.1097/MD.0000000000013298 Text en Copyright © 2019 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by/4.0 This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/4.0. |
spellingShingle | Research Article Yang, Yibo Wang, Jing Li, Hui Liu, Lihong Yao, Maojin Xiao, Tao Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis |
title | Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis |
title_full | Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis |
title_fullStr | Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis |
title_full_unstemmed | Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis |
title_short | Association between prognosis and SEMA4D/Plexin-B1 expression in various malignancies: A meta-analysis |
title_sort | association between prognosis and sema4d/plexin-b1 expression in various malignancies: a meta-analysis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6407964/ https://www.ncbi.nlm.nih.gov/pubmed/30762724 http://dx.doi.org/10.1097/MD.0000000000013298 |
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