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A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma
Cytoglobin (CYGB) is a ubiquitously expressed protein with a protective role against oxidative stress, fibrosis and tumor growth, shown to be transcriptionally regulated under hypoxic conditions. Hypoxia-inducible CYGB expression is observed in several cancer cell lines and particularly in various m...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149659/ https://www.ncbi.nlm.nih.gov/pubmed/34035373 http://dx.doi.org/10.1038/s41598-021-90284-6 |
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author | De Backer, Joey Maric, Darko Bosman, Matthias Dewilde, Sylvia Hoogewijs, David |
author_facet | De Backer, Joey Maric, Darko Bosman, Matthias Dewilde, Sylvia Hoogewijs, David |
author_sort | De Backer, Joey |
collection | PubMed |
description | Cytoglobin (CYGB) is a ubiquitously expressed protein with a protective role against oxidative stress, fibrosis and tumor growth, shown to be transcriptionally regulated under hypoxic conditions. Hypoxia-inducible CYGB expression is observed in several cancer cell lines and particularly in various melanoma-derived cell lines. However, reliable detection of hypoxia-inducible mRNA levels by qPCR depends on the critical choice of suitable reference genes for accurate normalization. Limited evidence exists to support selection of the commonly used reference genes in hypoxic models of melanoma. This study aimed to select the optimal reference genes to study CYGB expression levels in melanoma cell lines exposed to hypoxic conditions (0.2% O(2)) and to the HIF prolyl hydroxylase inhibitor roxadustat (FG-4592). The expression levels of candidate genes were assessed by qPCR and the stability of genes was evaluated using the geNorm and NormFinder algorithms. Our results display that B2M and YWHAZ represent the most optimal reference genes to reliably quantify hypoxia-inducible CYGB expression in melanoma cell lines. We further validate hypoxia-inducible CYGB expression on protein level and by using CYGB promoter-driven luciferase reporter assays in melanoma cell lines. |
format | Online Article Text |
id | pubmed-8149659 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-81496592021-05-26 A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma De Backer, Joey Maric, Darko Bosman, Matthias Dewilde, Sylvia Hoogewijs, David Sci Rep Article Cytoglobin (CYGB) is a ubiquitously expressed protein with a protective role against oxidative stress, fibrosis and tumor growth, shown to be transcriptionally regulated under hypoxic conditions. Hypoxia-inducible CYGB expression is observed in several cancer cell lines and particularly in various melanoma-derived cell lines. However, reliable detection of hypoxia-inducible mRNA levels by qPCR depends on the critical choice of suitable reference genes for accurate normalization. Limited evidence exists to support selection of the commonly used reference genes in hypoxic models of melanoma. This study aimed to select the optimal reference genes to study CYGB expression levels in melanoma cell lines exposed to hypoxic conditions (0.2% O(2)) and to the HIF prolyl hydroxylase inhibitor roxadustat (FG-4592). The expression levels of candidate genes were assessed by qPCR and the stability of genes was evaluated using the geNorm and NormFinder algorithms. Our results display that B2M and YWHAZ represent the most optimal reference genes to reliably quantify hypoxia-inducible CYGB expression in melanoma cell lines. We further validate hypoxia-inducible CYGB expression on protein level and by using CYGB promoter-driven luciferase reporter assays in melanoma cell lines. Nature Publishing Group UK 2021-05-25 /pmc/articles/PMC8149659/ /pubmed/34035373 http://dx.doi.org/10.1038/s41598-021-90284-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article De Backer, Joey Maric, Darko Bosman, Matthias Dewilde, Sylvia Hoogewijs, David A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
title | A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
title_full | A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
title_fullStr | A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
title_full_unstemmed | A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
title_short | A reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
title_sort | reliable set of reference genes to normalize oxygen-dependent cytoglobin gene expression levels in melanoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8149659/ https://www.ncbi.nlm.nih.gov/pubmed/34035373 http://dx.doi.org/10.1038/s41598-021-90284-6 |
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