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Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis

BACKGROUND: The prognostic significance of insulin‐like growth factor binding protein 2 (IGFBP2) expression has been explored in plenty of studies in human cancers. Because of the controversial results, the meta‐analysis was carried out to evaluate the relevance of IGFBP2 expression with the prognos...

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Autores principales: Zhang, Biao, Hong, Chao‐Qun, Luo, Yu‐Hao, Wei, Lai‐Feng, Luo, Yun, Peng, Yu‐Hui, Xu, Yi‐Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385590/
https://www.ncbi.nlm.nih.gov/pubmed/35546443
http://dx.doi.org/10.1002/cam4.4680
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author Zhang, Biao
Hong, Chao‐Qun
Luo, Yu‐Hao
Wei, Lai‐Feng
Luo, Yun
Peng, Yu‐Hui
Xu, Yi‐Wei
author_facet Zhang, Biao
Hong, Chao‐Qun
Luo, Yu‐Hao
Wei, Lai‐Feng
Luo, Yun
Peng, Yu‐Hui
Xu, Yi‐Wei
author_sort Zhang, Biao
collection PubMed
description BACKGROUND: The prognostic significance of insulin‐like growth factor binding protein 2 (IGFBP2) expression has been explored in plenty of studies in human cancers. Because of the controversial results, the meta‐analysis was carried out to evaluate the relevance of IGFBP2 expression with the prognosis in various tumors. METHODS: The data searched from four databases (Pubmed, Embase, Cochrane library, and Web of science) was used to calculate pooled hazard ratios (HRs) in this meta‐analysis. Subgroup analyses were stratified by ethnicity, cancer type, publication year, Newcastle–Ottawa Scale score, treatments, and populations. RESULTS: Twenty‐one studies containing 5560 patients finally met inclusion criteria. IGFBP2 expression was associated with lower overall survival (HR = 1.57, 95% CI = 1.31–1.88) and progression‐free survival (HR = 1.18, 95% CI = 1.04–1.34) in cancer patients, but not with disease‐free survival (HR = 1.50, 95% CI = 0.91–2.46) or recurrence‐free survival (HR = 1.50, 95% CI = 0.93–2.40). The subgroup analyses indicated IGFBP2 overexpression was significantly correlated with overall survival in Asian patients (HR = 1.42, 95% CI = 1.18–1.72), Caucasian patients (HR = 2.20, 95% CI = 1.31–3.70), glioma (HR = 1.36, 95% CI = 1.03–1.79), and colorectal cancer (HR = 2.52, 95% CI = 1.43–4.44) and surgery subgroups (HR = 1.97, 95% CI = 1.50–2.58). CONCLUSION: The meta‐analysis showed that IGFBP2 expression was associated with worse prognosis in several tumors, and may serve as a potential prognostic biomarker in cancer patients.
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spelling pubmed-93855902022-08-19 Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis Zhang, Biao Hong, Chao‐Qun Luo, Yu‐Hao Wei, Lai‐Feng Luo, Yun Peng, Yu‐Hui Xu, Yi‐Wei Cancer Med REVIEW BACKGROUND: The prognostic significance of insulin‐like growth factor binding protein 2 (IGFBP2) expression has been explored in plenty of studies in human cancers. Because of the controversial results, the meta‐analysis was carried out to evaluate the relevance of IGFBP2 expression with the prognosis in various tumors. METHODS: The data searched from four databases (Pubmed, Embase, Cochrane library, and Web of science) was used to calculate pooled hazard ratios (HRs) in this meta‐analysis. Subgroup analyses were stratified by ethnicity, cancer type, publication year, Newcastle–Ottawa Scale score, treatments, and populations. RESULTS: Twenty‐one studies containing 5560 patients finally met inclusion criteria. IGFBP2 expression was associated with lower overall survival (HR = 1.57, 95% CI = 1.31–1.88) and progression‐free survival (HR = 1.18, 95% CI = 1.04–1.34) in cancer patients, but not with disease‐free survival (HR = 1.50, 95% CI = 0.91–2.46) or recurrence‐free survival (HR = 1.50, 95% CI = 0.93–2.40). The subgroup analyses indicated IGFBP2 overexpression was significantly correlated with overall survival in Asian patients (HR = 1.42, 95% CI = 1.18–1.72), Caucasian patients (HR = 2.20, 95% CI = 1.31–3.70), glioma (HR = 1.36, 95% CI = 1.03–1.79), and colorectal cancer (HR = 2.52, 95% CI = 1.43–4.44) and surgery subgroups (HR = 1.97, 95% CI = 1.50–2.58). CONCLUSION: The meta‐analysis showed that IGFBP2 expression was associated with worse prognosis in several tumors, and may serve as a potential prognostic biomarker in cancer patients. John Wiley and Sons Inc. 2022-05-11 /pmc/articles/PMC9385590/ /pubmed/35546443 http://dx.doi.org/10.1002/cam4.4680 Text en © 2022 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle REVIEW
Zhang, Biao
Hong, Chao‐Qun
Luo, Yu‐Hao
Wei, Lai‐Feng
Luo, Yun
Peng, Yu‐Hui
Xu, Yi‐Wei
Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis
title Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis
title_full Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis
title_fullStr Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis
title_full_unstemmed Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis
title_short Prognostic value of IGFBP2 in various cancers: a systematic review and meta‐analysis
title_sort prognostic value of igfbp2 in various cancers: a systematic review and meta‐analysis
topic REVIEW
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385590/
https://www.ncbi.nlm.nih.gov/pubmed/35546443
http://dx.doi.org/10.1002/cam4.4680
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