Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer
Main Author: | |
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Publication Date: | 2023 |
Other Authors: | , , , , |
Format: | Article |
Language: | eng |
Source: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Download full: | http://hdl.handle.net/10400.17/4799 |
Summary: | Pancreatic cancer is anticipated to be the second leading cause of cancer-related death by 2030. Aquaporins (AQPs), a family of water channel proteins, have been linked to carcinogenesis. The aim of this study was to determine AQP gene expression in pancreatic cancer tissues and to validate aquaporins as possible diagnosis and/or prognosis genes. The relative gene expression levels of AQP1, AQP3, AQP5, and AQP9 were analyzed using real-time quantitative PCR (RT-qPCR) in 24 paired pancreatic tumors and adjacent healthy tissues according to variables such as age, gender, and tumor invasiveness and aggressiveness. AQPs transcripts were detected in both healthy and tumor tissues. While AQP1 was downregulated in the tumor samples, AQP3 was particularly overexpressed in low-grade invasive tumors. Interestingly, most of the strong positive Pearson correlation coefficients found between AQPs in healthy tissues were lost when analyzing the tumor tissues, suggesting disruption of the coordinated AQP-gene expression in pancreatic cancer. |
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Aquaporins Transcripts with Potential Prognostic Value in Pancreatic CancerAggressionAquaporins* / geneticsHumansPancreatic Neoplasms* / geneticsPrognosisHCC CHBPTPancreatic cancer is anticipated to be the second leading cause of cancer-related death by 2030. Aquaporins (AQPs), a family of water channel proteins, have been linked to carcinogenesis. The aim of this study was to determine AQP gene expression in pancreatic cancer tissues and to validate aquaporins as possible diagnosis and/or prognosis genes. The relative gene expression levels of AQP1, AQP3, AQP5, and AQP9 were analyzed using real-time quantitative PCR (RT-qPCR) in 24 paired pancreatic tumors and adjacent healthy tissues according to variables such as age, gender, and tumor invasiveness and aggressiveness. AQPs transcripts were detected in both healthy and tumor tissues. While AQP1 was downregulated in the tumor samples, AQP3 was particularly overexpressed in low-grade invasive tumors. Interestingly, most of the strong positive Pearson correlation coefficients found between AQPs in healthy tissues were lost when analyzing the tumor tissues, suggesting disruption of the coordinated AQP-gene expression in pancreatic cancer.Multidisciplinary Digital Publishing Institute (MDPI)Repositório da Unidade Local de Saúde São JoséLopes, PAFonseca, Eda Silva, IVVigia, EPaulino, JSoveral, G2024-02-09T14:48:52Z20232023-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.17/4799eng10.3390/genes14091694info:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-03-06T16:47:49Zoai:repositorio.chlc.pt:10400.17/4799Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T00:18:53.533127Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
title |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
spellingShingle |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer Lopes, PA Aggression Aquaporins* / genetics Humans Pancreatic Neoplasms* / genetics Prognosis HCC CHBPT |
title_short |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
title_full |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
title_fullStr |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
title_full_unstemmed |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
title_sort |
Aquaporins Transcripts with Potential Prognostic Value in Pancreatic Cancer |
author |
Lopes, PA |
author_facet |
Lopes, PA Fonseca, E da Silva, IV Vigia, E Paulino, J Soveral, G |
author_role |
author |
author2 |
Fonseca, E da Silva, IV Vigia, E Paulino, J Soveral, G |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Repositório da Unidade Local de Saúde São José |
dc.contributor.author.fl_str_mv |
Lopes, PA Fonseca, E da Silva, IV Vigia, E Paulino, J Soveral, G |
dc.subject.por.fl_str_mv |
Aggression Aquaporins* / genetics Humans Pancreatic Neoplasms* / genetics Prognosis HCC CHBPT |
topic |
Aggression Aquaporins* / genetics Humans Pancreatic Neoplasms* / genetics Prognosis HCC CHBPT |
description |
Pancreatic cancer is anticipated to be the second leading cause of cancer-related death by 2030. Aquaporins (AQPs), a family of water channel proteins, have been linked to carcinogenesis. The aim of this study was to determine AQP gene expression in pancreatic cancer tissues and to validate aquaporins as possible diagnosis and/or prognosis genes. The relative gene expression levels of AQP1, AQP3, AQP5, and AQP9 were analyzed using real-time quantitative PCR (RT-qPCR) in 24 paired pancreatic tumors and adjacent healthy tissues according to variables such as age, gender, and tumor invasiveness and aggressiveness. AQPs transcripts were detected in both healthy and tumor tissues. While AQP1 was downregulated in the tumor samples, AQP3 was particularly overexpressed in low-grade invasive tumors. Interestingly, most of the strong positive Pearson correlation coefficients found between AQPs in healthy tissues were lost when analyzing the tumor tissues, suggesting disruption of the coordinated AQP-gene expression in pancreatic cancer. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023 2023-01-01T00:00:00Z 2024-02-09T14:48:52Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10400.17/4799 |
url |
http://hdl.handle.net/10400.17/4799 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.3390/genes14091694 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute (MDPI) |
publisher.none.fl_str_mv |
Multidisciplinary Digital Publishing Institute (MDPI) |
dc.source.none.fl_str_mv |
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