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Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers

Esophageal, gastric, liver, and colorectal cancers represent four prevalent gastrointestinal cancers that pose substantial threats to global health due to their high morbidity and mortality rates. Peroxiredoxin 1 (PRDX1), a significant component of the PRDXs family, primarily functions to counteract...

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Autores principales: Zhang, Zhou, Zhou, Pengli, Liu, Mingyue, Pei, Bing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539570/
https://www.ncbi.nlm.nih.gov/pubmed/37781072
http://dx.doi.org/10.7150/jca.86568
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author Zhang, Zhou
Zhou, Pengli
Liu, Mingyue
Pei, Bing
author_facet Zhang, Zhou
Zhou, Pengli
Liu, Mingyue
Pei, Bing
author_sort Zhang, Zhou
collection PubMed
description Esophageal, gastric, liver, and colorectal cancers represent four prevalent gastrointestinal cancers that pose substantial threats to global health due to their high morbidity and mortality rates. Peroxiredoxin 1 (PRDX1), a significant component of the PRDXs family, primarily functions to counteract the peroxides produced by metabolic activities in the body, thereby maintaining the dynamic equilibrium of peroxides in vivo. Intriguingly, PRDX1 expression correlates strongly with cancer's onset, progression, and prognosis. This study mainly applied bioinformatics methods to analyze PRDX1's expression, diagnosis, and prognosis in gastrointestinal cancers and to summarize current research advancements. Evidence from the bioinformatics database suggested that the high expression of PRDX1 was a prominent characteristic of these four gastrointestinal cancers, with this observation reaching statistical significance. The high expression of PRDX1 in gastrointestinal cancer cells also confirms this result. Notably, the primary alteration in PRDX1 within these cancers is the presence of genetic mutations. PRDX1 demonstrated the highest diagnostic efficacy for colorectal cancer. Nevertheless, elevated PRDX1 levels only significantly diminished the survival time of liver cancer patients, exerting no statistically significant impact on the survival duration of patients afflicted by the other three types of gastrointestinal cancers. Recent research has indicated variability in PRDX1 expression across different cancer types, with high expression being predominantly observed in these four gastrointestinal cancers and, in most instances, unfavorable prognosis. These findings broadly align with the results derived from bioinformatics. This research underscores the high expression of PRDX1 in gastrointestinal cancers, its relevance to the diagnosis and prognosis monitoring of these cancers, and its potential to guide clinical treatment for these cancers.
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spelling pubmed-105395702023-09-30 Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers Zhang, Zhou Zhou, Pengli Liu, Mingyue Pei, Bing J Cancer Research Paper Esophageal, gastric, liver, and colorectal cancers represent four prevalent gastrointestinal cancers that pose substantial threats to global health due to their high morbidity and mortality rates. Peroxiredoxin 1 (PRDX1), a significant component of the PRDXs family, primarily functions to counteract the peroxides produced by metabolic activities in the body, thereby maintaining the dynamic equilibrium of peroxides in vivo. Intriguingly, PRDX1 expression correlates strongly with cancer's onset, progression, and prognosis. This study mainly applied bioinformatics methods to analyze PRDX1's expression, diagnosis, and prognosis in gastrointestinal cancers and to summarize current research advancements. Evidence from the bioinformatics database suggested that the high expression of PRDX1 was a prominent characteristic of these four gastrointestinal cancers, with this observation reaching statistical significance. The high expression of PRDX1 in gastrointestinal cancer cells also confirms this result. Notably, the primary alteration in PRDX1 within these cancers is the presence of genetic mutations. PRDX1 demonstrated the highest diagnostic efficacy for colorectal cancer. Nevertheless, elevated PRDX1 levels only significantly diminished the survival time of liver cancer patients, exerting no statistically significant impact on the survival duration of patients afflicted by the other three types of gastrointestinal cancers. Recent research has indicated variability in PRDX1 expression across different cancer types, with high expression being predominantly observed in these four gastrointestinal cancers and, in most instances, unfavorable prognosis. These findings broadly align with the results derived from bioinformatics. This research underscores the high expression of PRDX1 in gastrointestinal cancers, its relevance to the diagnosis and prognosis monitoring of these cancers, and its potential to guide clinical treatment for these cancers. Ivyspring International Publisher 2023-09-11 /pmc/articles/PMC10539570/ /pubmed/37781072 http://dx.doi.org/10.7150/jca.86568 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Zhang, Zhou
Zhou, Pengli
Liu, Mingyue
Pei, Bing
Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers
title Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers
title_full Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers
title_fullStr Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers
title_full_unstemmed Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers
title_short Expression And Prognostic Role of PRDX1 In Gastrointestinal Cancers
title_sort expression and prognostic role of prdx1 in gastrointestinal cancers
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10539570/
https://www.ncbi.nlm.nih.gov/pubmed/37781072
http://dx.doi.org/10.7150/jca.86568
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