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The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis

BACKGROUND: Bladder cancer is one of the most common urological cancers all over the world, and NMIBC occupies almost 80% of recently diagnosed bladder cancer cases. Progress and recurrence of bladder cancer are the main problems during the disease. The level of TP53 mutation is obviously higher in...

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Autores principales: Liao, Yihao, Tang, Huiqin, Wang, Miaomiao, Wang, Keke, Wang, Youzhi, Jiang, Ning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128305/
https://www.ncbi.nlm.nih.gov/pubmed/33780049
http://dx.doi.org/10.1002/jcla.23765
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author Liao, Yihao
Tang, Huiqin
Wang, Miaomiao
Wang, Keke
Wang, Youzhi
Jiang, Ning
author_facet Liao, Yihao
Tang, Huiqin
Wang, Miaomiao
Wang, Keke
Wang, Youzhi
Jiang, Ning
author_sort Liao, Yihao
collection PubMed
description BACKGROUND: Bladder cancer is one of the most common urological cancers all over the world, and NMIBC occupies almost 80% of recently diagnosed bladder cancer cases. Progress and recurrence of bladder cancer are the main problems during the disease. The level of TP53 mutation is obviously higher in the high stage than the lower. This meta‐analysis is to evaluate the potential diagnosis feature of TP53 mutation by the expression of TP53 mutation of Ta stage vs high stage in bladder cancer. METHODS: A systematic search of databases was conducted, and some relevant articles were selected. Next, the meta‐analysis was carried out according to the standard guidelines. RESULTS: There were seven researches in which 677 participants were selected at the basis of inclusion standard. TP53 mutation was associated highly with increased diagnosis of bladder cancer. We found that the high stage of bladder cancer has obviously higher level of TP53 mutation than the lower stage, and these patients of MIBC have higher expression of TP53 mutation compared with NMIBC. No significant publication bias has been observed in this meta‐analysis. The expression of TP53 mutation might be a diagnose‐related biomarker for lots of patients with bladder cancer. CONCLUSIONS: The results of this meta‐analysis provided further evidences that the expression of TP53 mutation was associated with the diagnosis efficiency of advanced bladder cancer. Higher expression of TP53 mutation was observed in the high stage of bladder cancer or the MIBC, and lower expression of TP53 mutation in the Ta stage of bladder cancer or the NMIBC. The expression level of TP53 mutation was probably a critical diagnosed biomarker in advanced bladder cancer.
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spelling pubmed-81283052021-05-21 The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis Liao, Yihao Tang, Huiqin Wang, Miaomiao Wang, Keke Wang, Youzhi Jiang, Ning J Clin Lab Anal Research Articles BACKGROUND: Bladder cancer is one of the most common urological cancers all over the world, and NMIBC occupies almost 80% of recently diagnosed bladder cancer cases. Progress and recurrence of bladder cancer are the main problems during the disease. The level of TP53 mutation is obviously higher in the high stage than the lower. This meta‐analysis is to evaluate the potential diagnosis feature of TP53 mutation by the expression of TP53 mutation of Ta stage vs high stage in bladder cancer. METHODS: A systematic search of databases was conducted, and some relevant articles were selected. Next, the meta‐analysis was carried out according to the standard guidelines. RESULTS: There were seven researches in which 677 participants were selected at the basis of inclusion standard. TP53 mutation was associated highly with increased diagnosis of bladder cancer. We found that the high stage of bladder cancer has obviously higher level of TP53 mutation than the lower stage, and these patients of MIBC have higher expression of TP53 mutation compared with NMIBC. No significant publication bias has been observed in this meta‐analysis. The expression of TP53 mutation might be a diagnose‐related biomarker for lots of patients with bladder cancer. CONCLUSIONS: The results of this meta‐analysis provided further evidences that the expression of TP53 mutation was associated with the diagnosis efficiency of advanced bladder cancer. Higher expression of TP53 mutation was observed in the high stage of bladder cancer or the MIBC, and lower expression of TP53 mutation in the Ta stage of bladder cancer or the NMIBC. The expression level of TP53 mutation was probably a critical diagnosed biomarker in advanced bladder cancer. John Wiley and Sons Inc. 2021-03-29 /pmc/articles/PMC8128305/ /pubmed/33780049 http://dx.doi.org/10.1002/jcla.23765 Text en © 2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC 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 Research Articles
Liao, Yihao
Tang, Huiqin
Wang, Miaomiao
Wang, Keke
Wang, Youzhi
Jiang, Ning
The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis
title The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis
title_full The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis
title_fullStr The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis
title_full_unstemmed The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis
title_short The potential diagnosis role of TP53 mutation in advanced bladder cancer: A meta‐analysis
title_sort potential diagnosis role of tp53 mutation in advanced bladder cancer: a meta‐analysis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128305/
https://www.ncbi.nlm.nih.gov/pubmed/33780049
http://dx.doi.org/10.1002/jcla.23765
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