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TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis

Recent studies have showed that the transforming acidic coiled coil 3 (TACC3), was aberrantly up-regulated in various solid tumors and was reported to be correlated with unfavorable prognosis in cancer patients. This study aimed to examine the relationship between TACC3 and relevant clinical outcome...

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Autores principales: Wang, June, Du, Shenlin, Fan, Wei, Wang, Ping, Yang, Weiqing, Yu, Mingxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650442/
https://www.ncbi.nlm.nih.gov/pubmed/29088887
http://dx.doi.org/10.18632/oncotarget.20466
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author Wang, June
Du, Shenlin
Fan, Wei
Wang, Ping
Yang, Weiqing
Yu, Mingxia
author_facet Wang, June
Du, Shenlin
Fan, Wei
Wang, Ping
Yang, Weiqing
Yu, Mingxia
author_sort Wang, June
collection PubMed
description Recent studies have showed that the transforming acidic coiled coil 3 (TACC3), was aberrantly up-regulated in various solid tumors and was reported to be correlated with unfavorable prognosis in cancer patients. This study aimed to examine the relationship between TACC3 and relevant clinical outcomes. Pubmed, Web of Science, Embase and Cochrane Library were systematically searched to obtain all eligible articles. Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to evaluate the influence of TACC3 expression on overall survival (OS) and disease-free survival (DFS) in solid tumors patients. A total of 1943 patients from 11 articles were included. The result indicated that a significantly shorter OS was observed in patients with high expression level of TACC3 (HR=1.90, 95% CI=1.63–2.23). In the subgroup analysis, the association was also observed in patients with cancers of digestive system (HR=1.85, 95% CI=1.53–2.24). Statistical significance was also observed in subgroup meta-analysis stratified by the cancer type, analysis type and sample size. Furthermore, poorer DFS was observed in patients with high expression level of TACC3 (HR=2.67, 95% CI=2.10–3.40). Additionally, the pooled odds ratios (ORs) showed that increased TACC3 expression was also related to positive lymph node metastasis (OR=1.68, 95% CI=1.26–2.25), tumor differentiation (OR=1.90, 95% CI=1.25–2.88) and TNM stage (OR=1.66, 95% CI=1.25-2.20). In conclusion, the increased expression level of TACC3 was associated with unfavorable prognosis, suggesting that it was a valuable prognosis biomarker or a promising therapeutic target of solid tumors. Further studies should be conducted to confirm the clinical utility of TACC3 in human solid tumors.
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spelling pubmed-56504422017-10-30 TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis Wang, June Du, Shenlin Fan, Wei Wang, Ping Yang, Weiqing Yu, Mingxia Oncotarget Meta-Analysis Recent studies have showed that the transforming acidic coiled coil 3 (TACC3), was aberrantly up-regulated in various solid tumors and was reported to be correlated with unfavorable prognosis in cancer patients. This study aimed to examine the relationship between TACC3 and relevant clinical outcomes. Pubmed, Web of Science, Embase and Cochrane Library were systematically searched to obtain all eligible articles. Pooled hazard ratios (HRs) and 95% confidence intervals (CIs) were calculated to evaluate the influence of TACC3 expression on overall survival (OS) and disease-free survival (DFS) in solid tumors patients. A total of 1943 patients from 11 articles were included. The result indicated that a significantly shorter OS was observed in patients with high expression level of TACC3 (HR=1.90, 95% CI=1.63–2.23). In the subgroup analysis, the association was also observed in patients with cancers of digestive system (HR=1.85, 95% CI=1.53–2.24). Statistical significance was also observed in subgroup meta-analysis stratified by the cancer type, analysis type and sample size. Furthermore, poorer DFS was observed in patients with high expression level of TACC3 (HR=2.67, 95% CI=2.10–3.40). Additionally, the pooled odds ratios (ORs) showed that increased TACC3 expression was also related to positive lymph node metastasis (OR=1.68, 95% CI=1.26–2.25), tumor differentiation (OR=1.90, 95% CI=1.25–2.88) and TNM stage (OR=1.66, 95% CI=1.25-2.20). In conclusion, the increased expression level of TACC3 was associated with unfavorable prognosis, suggesting that it was a valuable prognosis biomarker or a promising therapeutic target of solid tumors. Further studies should be conducted to confirm the clinical utility of TACC3 in human solid tumors. Impact Journals LLC 2017-08-24 /pmc/articles/PMC5650442/ /pubmed/29088887 http://dx.doi.org/10.18632/oncotarget.20466 Text en Copyright: © 2017 Wang 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 (http://creativecommons.org/licenses/by/3.0/) 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 Meta-Analysis
Wang, June
Du, Shenlin
Fan, Wei
Wang, Ping
Yang, Weiqing
Yu, Mingxia
TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
title TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
title_full TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
title_fullStr TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
title_full_unstemmed TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
title_short TACC3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
title_sort tacc3 as an independent prognostic marker for solid tumors: a systematic review and meta-analysis
topic Meta-Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5650442/
https://www.ncbi.nlm.nih.gov/pubmed/29088887
http://dx.doi.org/10.18632/oncotarget.20466
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