Gene Expression and Prognostic Value of NADPH Oxidase Enzymes in Breast Cancer
NADPH oxidase enzymes (NOX) are involved in all stages of carcinogenesis, but their expression levels and prognostic value in breast cancer (BC) remain unclear. Thus, we aimed to assess the expression and prognostic value of NOX enzymes in BC samples using online databases. For this, mRNA expression...
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description | NADPH oxidase enzymes (NOX) are involved in all stages of carcinogenesis, but their expression levels and prognostic value in breast cancer (BC) remain unclear. Thus, we aimed to assess the expression and prognostic value of NOX enzymes in BC samples using online databases. For this, mRNA expression from 290 normal breast tissue samples and 1904 BC samples obtained from studies on cBioPortal, Kaplan-Meier Plotter, and The Human Protein Atlas were analyzed. We found higher levels of NOX2, NOX4, and Dual oxidase 1 (DUOX1) in normal breast tissue. NOX1, NOX2, and NOX4 exhibited higher expression in BC, except for the basal subtype, where NOX4 expression was lower. DUOX1 mRNA levels were lower in all BC subtypes. NOX2, NOX4, and NOX5 mRNA levels increased with tumor progression stages, while NOX1 and DUOX1 expression decreased in more advanced stages. Moreover, patients with low expression of NOX1, NOX4, and DUOX1 had lower survival rates than those with high expression of these enzymes. In conclusion, our data suggest an overexpression of NOX enzymes in breast cancer, with certain isoforms showing a positive correlation with tumor progression. |
doi_str_mv | 10.3390/ijms25063464 |
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Thus, we aimed to assess the expression and prognostic value of NOX enzymes in BC samples using online databases. For this, mRNA expression from 290 normal breast tissue samples and 1904 BC samples obtained from studies on cBioPortal, Kaplan-Meier Plotter, and The Human Protein Atlas were analyzed. We found higher levels of NOX2, NOX4, and Dual oxidase 1 (DUOX1) in normal breast tissue. NOX1, NOX2, and NOX4 exhibited higher expression in BC, except for the basal subtype, where NOX4 expression was lower. DUOX1 mRNA levels were lower in all BC subtypes. NOX2, NOX4, and NOX5 mRNA levels increased with tumor progression stages, while NOX1 and DUOX1 expression decreased in more advanced stages. Moreover, patients with low expression of NOX1, NOX4, and DUOX1 had lower survival rates than those with high expression of these enzymes. In conclusion, our data suggest an overexpression of NOX enzymes in breast cancer, with certain isoforms showing a positive correlation with tumor progression.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms25063464</identifier><identifier>PMID: 38542437</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Binding sites ; Breast cancer ; Breast Neoplasms - genetics ; Cancer ; Communication ; Development and progression ; Dual Oxidases - genetics ; Enzymes ; Estrogens ; Female ; Gene Expression ; Genetic aspects ; Humans ; Medical prognosis ; Metastasis ; NADPH Oxidase 1 - genetics ; NADPH Oxidase 4 - genetics ; NADPH Oxidases - genetics ; NADPH Oxidases - metabolism ; Online databases ; Oxidases ; Physiology ; Prognosis ; Reactive Oxygen Species - metabolism ; RNA ; RNA, Messenger - genetics ; Survival analysis</subject><ispartof>International journal of molecular sciences, 2024-03, Vol.25 (6), p.3464</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. 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/). 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Thus, we aimed to assess the expression and prognostic value of NOX enzymes in BC samples using online databases. For this, mRNA expression from 290 normal breast tissue samples and 1904 BC samples obtained from studies on cBioPortal, Kaplan-Meier Plotter, and The Human Protein Atlas were analyzed. We found higher levels of NOX2, NOX4, and Dual oxidase 1 (DUOX1) in normal breast tissue. NOX1, NOX2, and NOX4 exhibited higher expression in BC, except for the basal subtype, where NOX4 expression was lower. DUOX1 mRNA levels were lower in all BC subtypes. NOX2, NOX4, and NOX5 mRNA levels increased with tumor progression stages, while NOX1 and DUOX1 expression decreased in more advanced stages. Moreover, patients with low expression of NOX1, NOX4, and DUOX1 had lower survival rates than those with high expression of these enzymes. In conclusion, our data suggest an overexpression of NOX enzymes in breast cancer, with certain isoforms showing a positive correlation with tumor progression.</description><subject>Binding sites</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - genetics</subject><subject>Cancer</subject><subject>Communication</subject><subject>Development and progression</subject><subject>Dual Oxidases - genetics</subject><subject>Enzymes</subject><subject>Estrogens</subject><subject>Female</subject><subject>Gene Expression</subject><subject>Genetic aspects</subject><subject>Humans</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>NADPH Oxidase 1 - genetics</subject><subject>NADPH Oxidase 4 - genetics</subject><subject>NADPH Oxidases - genetics</subject><subject>NADPH Oxidases - metabolism</subject><subject>Online databases</subject><subject>Oxidases</subject><subject>Physiology</subject><subject>Prognosis</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RNA</subject><subject>RNA, Messenger - genetics</subject><subject>Survival analysis</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptks1v1DAQxSNERUvLjTOyxIVDt0zsydo5oWVbWqSq7aFwtRxnsniV2IudoJa_Hlf9YIuQD7bGv_dGz56ieFvCkRA1fHTrIfEK5gLn-KLYK5HzGcBcvtw67xavU1oDcMGr-lWxK1SFHIXcKy5OyRM7udlESskFz4xv2VUMKx_S6Cz7bvqJWOjYxeL46oxd3rjWpCzwv28HSsx59jmSSSNbGm8pHhQ7nekTvXnY94tvX06ul2ez88vTr8vF-czmruPMKCwVIKgGkSRAlQvW8tKitFihqBuLzRwkSWVMBxWprq6xQYnY5lAk9otP976bqRmoteTHaHq9iW4w8VYH4_TzG-9-6FX4pUuoJShZZocPDw4x_JwojXpwyVLfG09hSlpAiQCykjKj7_9B12GKPufLFAgQHDj8pVamJ-18F3Jje2eqF1IpjgpBZOroP1ReLQ3OBk-dy_VngsN7gY0hpUjdU8gS9N0A6O0ByPi77Yd5gh9_XPwB0SyohA</recordid><startdate>20240319</startdate><enddate>20240319</enddate><creator>de Vasconcelos E Souza, Andressa</creator><creator>de Faria, Caroline Coelho</creator><creator>Pereira, Leonardo Matta</creator><creator>Ferreira, Andrea Claudia Freitas</creator><creator>Torres, Pedro Henrique Monteiro</creator><creator>Fortunato, Rodrigo Soares</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-4194-4510</orcidid><orcidid>https://orcid.org/0000-0002-0945-1495</orcidid><orcidid>https://orcid.org/0000-0001-7300-2718</orcidid><orcidid>https://orcid.org/0000-0003-3497-8173</orcidid></search><sort><creationdate>20240319</creationdate><title>Gene Expression and Prognostic Value of NADPH Oxidase Enzymes in Breast Cancer</title><author>de Vasconcelos E Souza, Andressa ; 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Thus, we aimed to assess the expression and prognostic value of NOX enzymes in BC samples using online databases. For this, mRNA expression from 290 normal breast tissue samples and 1904 BC samples obtained from studies on cBioPortal, Kaplan-Meier Plotter, and The Human Protein Atlas were analyzed. We found higher levels of NOX2, NOX4, and Dual oxidase 1 (DUOX1) in normal breast tissue. NOX1, NOX2, and NOX4 exhibited higher expression in BC, except for the basal subtype, where NOX4 expression was lower. DUOX1 mRNA levels were lower in all BC subtypes. NOX2, NOX4, and NOX5 mRNA levels increased with tumor progression stages, while NOX1 and DUOX1 expression decreased in more advanced stages. Moreover, patients with low expression of NOX1, NOX4, and DUOX1 had lower survival rates than those with high expression of these enzymes. 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subjects | Binding sites Breast cancer Breast Neoplasms - genetics Cancer Communication Development and progression Dual Oxidases - genetics Enzymes Estrogens Female Gene Expression Genetic aspects Humans Medical prognosis Metastasis NADPH Oxidase 1 - genetics NADPH Oxidase 4 - genetics NADPH Oxidases - genetics NADPH Oxidases - metabolism Online databases Oxidases Physiology Prognosis Reactive Oxygen Species - metabolism RNA RNA, Messenger - genetics Survival analysis |
title | Gene Expression and Prognostic Value of NADPH Oxidase Enzymes in Breast Cancer |
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