Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas

Superoxide dismutase 3 (SOD3) is a secreted antioxidant enzyme that regulates reactive oxygen species in the microenvironment. It is also a potential tumour suppressor gene that is significantly downregulated in breast cancer. We have previously shown that its mRNA expression is inversely correlated...

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Main Authors: Brandon Griess, David Klinkebiel, Alice Kueh, Michelle Desler, Kenneth Cowan, Matthew Fitzgerald, Melissa Teoh-Fitzgerald
Format: Article
Language:English
Published: Taylor & Francis Group 2020-12-01
Series:Epigenetics
Subjects:
Online Access:http://dx.doi.org/10.1080/15592294.2020.1777666
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author Brandon Griess
David Klinkebiel
Alice Kueh
Michelle Desler
Kenneth Cowan
Matthew Fitzgerald
Melissa Teoh-Fitzgerald
author_facet Brandon Griess
David Klinkebiel
Alice Kueh
Michelle Desler
Kenneth Cowan
Matthew Fitzgerald
Melissa Teoh-Fitzgerald
author_sort Brandon Griess
collection DOAJ
description Superoxide dismutase 3 (SOD3) is a secreted antioxidant enzyme that regulates reactive oxygen species in the microenvironment. It is also a potential tumour suppressor gene that is significantly downregulated in breast cancer. We have previously shown that its mRNA expression is inversely correlated with relapse free survival in breast cancer patients. This study aimed to investigate the correlation of SOD3 promoter DNA methylation with its expression in different molecular subtypes of breast carcinoma. We found that SOD3 expression was significantly reduced in breast carcinoma samples compared to normal tissues with the lowest levels observed in Luminal B subtype. Pyrosequencing analysis showed significant increase in methylation levels in the SOD3 promoter region (−108 and −19 from the TSS) in tumours vs normal tissues (53.6% vs 25.2%). The highest degree of correlation between methylation and SOD3 expression levels was observed in Luminal B subtype (Spearman’s R = −0.540, P < 0.00093). In this subtype, the −78 CpG position is the most significantly methylated site. The Spearman’s coefficient analysis also indicated the most significant correlation of DNA methylation at this site with SOD3 gene expression levels in tumours vs. normal tissues (R = −0.5816, P < 6.9E-12). Moreover, copy number variation analysis of TCGA database revealed that the more aggressive Triple Negative and Her2+ subtypes had higher levels of SOD3 gene deletion. The predominantly down-regulated expression pattern of SOD3 and the various genetic and epigenetic deregulations of its expression suggest that loss of this antioxidant promotes an advantageous tumour-promoting microenvironment in breast cancer.
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spelling doaj.art-f33701fa8eb74dab8168f550146f57d92023-09-21T13:09:23ZengTaylor & Francis GroupEpigenetics1559-22941559-23082020-12-0115121325133510.1080/15592294.2020.17776661777666Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomasBrandon Griess0David Klinkebiel1Alice Kueh2Michelle Desler3Kenneth Cowan4Matthew Fitzgerald5Melissa Teoh-Fitzgerald6University of Nebraska Medical CenterUniversity of Nebraska Medical CenterUniversity of Nebraska Medical CenterUniversity of Nebraska Medical CenterUniversity of Nebraska Medical CenterUniversity of Nebraska Medical CenterUniversity of Nebraska Medical CenterSuperoxide dismutase 3 (SOD3) is a secreted antioxidant enzyme that regulates reactive oxygen species in the microenvironment. It is also a potential tumour suppressor gene that is significantly downregulated in breast cancer. We have previously shown that its mRNA expression is inversely correlated with relapse free survival in breast cancer patients. This study aimed to investigate the correlation of SOD3 promoter DNA methylation with its expression in different molecular subtypes of breast carcinoma. We found that SOD3 expression was significantly reduced in breast carcinoma samples compared to normal tissues with the lowest levels observed in Luminal B subtype. Pyrosequencing analysis showed significant increase in methylation levels in the SOD3 promoter region (−108 and −19 from the TSS) in tumours vs normal tissues (53.6% vs 25.2%). The highest degree of correlation between methylation and SOD3 expression levels was observed in Luminal B subtype (Spearman’s R = −0.540, P < 0.00093). In this subtype, the −78 CpG position is the most significantly methylated site. The Spearman’s coefficient analysis also indicated the most significant correlation of DNA methylation at this site with SOD3 gene expression levels in tumours vs. normal tissues (R = −0.5816, P < 6.9E-12). Moreover, copy number variation analysis of TCGA database revealed that the more aggressive Triple Negative and Her2+ subtypes had higher levels of SOD3 gene deletion. The predominantly down-regulated expression pattern of SOD3 and the various genetic and epigenetic deregulations of its expression suggest that loss of this antioxidant promotes an advantageous tumour-promoting microenvironment in breast cancer.http://dx.doi.org/10.1080/15592294.2020.1777666sod3extracellular superoxide dismutasebreast cancerdna methylationpyrosequencing
spellingShingle Brandon Griess
David Klinkebiel
Alice Kueh
Michelle Desler
Kenneth Cowan
Matthew Fitzgerald
Melissa Teoh-Fitzgerald
Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas
Epigenetics
sod3
extracellular superoxide dismutase
breast cancer
dna methylation
pyrosequencing
title Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas
title_full Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas
title_fullStr Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas
title_full_unstemmed Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas
title_short Association ofSOD3 promoter DNA methylation with its down-regulation in breast carcinomas
title_sort association ofsod3 promoter dna methylation with its down regulation in breast carcinomas
topic sod3
extracellular superoxide dismutase
breast cancer
dna methylation
pyrosequencing
url http://dx.doi.org/10.1080/15592294.2020.1777666
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