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AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer

Breast cancer is still one of the leading causes of mortality in the female population. Despite the campaigns for early detection, the improvement in procedures and treatment, drastic improvement in survival rate is omitted. Discovery of aquaporins, at first described as cellular plumbing system, op...

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Detalles Bibliográficos
Autores principales: Milković, Lidija, Čipak Gašparović, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124745/
https://www.ncbi.nlm.nih.gov/pubmed/33947079
http://dx.doi.org/10.3390/molecules26092613
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author Milković, Lidija
Čipak Gašparović, Ana
author_facet Milković, Lidija
Čipak Gašparović, Ana
author_sort Milković, Lidija
collection PubMed
description Breast cancer is still one of the leading causes of mortality in the female population. Despite the campaigns for early detection, the improvement in procedures and treatment, drastic improvement in survival rate is omitted. Discovery of aquaporins, at first described as cellular plumbing system, opened new insights in processes which contribute to cancer cell motility and proliferation. As we discover new pathways activated by aquaporins, the more we realize the complexity of biological processes and the necessity to fully understand the pathways affected by specific aquaporin in order to gain the desired outcome–remission of the disease. Among the 13 human aquaporins, AQP3 and AQP5 were shown to be significantly upregulated in breast cancer indicating their role in the development of this malignancy. Therefore, these two aquaporins will be discussed for their involvement in breast cancer development, regulation of oxidative stress and redox signalling pathways leading to possibly targeting them for new therapies.
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spelling pubmed-81247452021-05-17 AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer Milković, Lidija Čipak Gašparović, Ana Molecules Review Breast cancer is still one of the leading causes of mortality in the female population. Despite the campaigns for early detection, the improvement in procedures and treatment, drastic improvement in survival rate is omitted. Discovery of aquaporins, at first described as cellular plumbing system, opened new insights in processes which contribute to cancer cell motility and proliferation. As we discover new pathways activated by aquaporins, the more we realize the complexity of biological processes and the necessity to fully understand the pathways affected by specific aquaporin in order to gain the desired outcome–remission of the disease. Among the 13 human aquaporins, AQP3 and AQP5 were shown to be significantly upregulated in breast cancer indicating their role in the development of this malignancy. Therefore, these two aquaporins will be discussed for their involvement in breast cancer development, regulation of oxidative stress and redox signalling pathways leading to possibly targeting them for new therapies. MDPI 2021-04-29 /pmc/articles/PMC8124745/ /pubmed/33947079 http://dx.doi.org/10.3390/molecules26092613 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Milković, Lidija
Čipak Gašparović, Ana
AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer
title AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer
title_full AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer
title_fullStr AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer
title_full_unstemmed AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer
title_short AQP3 and AQP5—Potential Regulators of Redox Status in Breast Cancer
title_sort aqp3 and aqp5—potential regulators of redox status in breast cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8124745/
https://www.ncbi.nlm.nih.gov/pubmed/33947079
http://dx.doi.org/10.3390/molecules26092613
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