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Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis
The Six Transmembrane Epithelial Antigen of the Prostate (STEAP1) is an oncogene overexpressed in several human tumors, particularly in prostate cancer (PCa). However, the mechanisms involved in its overexpression remain unknown. It is well known that epigenetic modifications may result in abnormal...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618799/ https://www.ncbi.nlm.nih.gov/pubmed/34833128 http://dx.doi.org/10.3390/life11111251 |
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author | Rocha, Sandra M. Sousa, Inês Gomes, Inês M. Arinto, Patrícia Costa-Pinheiro, Pedro Coutinho, Eduarda Santos, Cecília R. Jerónimo, Carmen Lemos, Manuel C. Passarinha, Luís A. Socorro, Sílvia Maia, Cláudio J. |
author_facet | Rocha, Sandra M. Sousa, Inês Gomes, Inês M. Arinto, Patrícia Costa-Pinheiro, Pedro Coutinho, Eduarda Santos, Cecília R. Jerónimo, Carmen Lemos, Manuel C. Passarinha, Luís A. Socorro, Sílvia Maia, Cláudio J. |
author_sort | Rocha, Sandra M. |
collection | PubMed |
description | The Six Transmembrane Epithelial Antigen of the Prostate (STEAP1) is an oncogene overexpressed in several human tumors, particularly in prostate cancer (PCa). However, the mechanisms involved in its overexpression remain unknown. It is well known that epigenetic modifications may result in abnormal gene expression patterns, contributing to tumor initiation and progression. Therefore, this study aimed to analyze the methylation pattern of the STEAP1 gene in PCa versus non-neoplastic cells. Bisulfite amplicon sequencing of the CpG island at the STEAP1 gene promoter showed a higher methylation level in non-neoplastic PNT1A prostate cells than in human PCa samples. Bioinformatic analysis of the GEO datasets also showed the STEAP1 gene promoter as being demethylated in human PCa, and a negative association with STEAP1 mRNA expression was observed. These results are supported by the treatment of non-neoplastic PNT1A cells with DNMT and HDAC inhibitors, which induced a significant increase in STEAP1 mRNA expression. In addition, the involvement of HDAC in the regulation of STEAP1 mRNA expression was corroborated by a negative association between STEAP1 mRNA expression and HDAC4,5,7 and 9 in human PCa. In conclusion, our work indicates that STEAP1 overexpression in PCa can be driven by the hypomethylation of STEAP1 gene promoter. |
format | Online Article Text |
id | pubmed-8618799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86187992021-11-27 Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis Rocha, Sandra M. Sousa, Inês Gomes, Inês M. Arinto, Patrícia Costa-Pinheiro, Pedro Coutinho, Eduarda Santos, Cecília R. Jerónimo, Carmen Lemos, Manuel C. Passarinha, Luís A. Socorro, Sílvia Maia, Cláudio J. Life (Basel) Article The Six Transmembrane Epithelial Antigen of the Prostate (STEAP1) is an oncogene overexpressed in several human tumors, particularly in prostate cancer (PCa). However, the mechanisms involved in its overexpression remain unknown. It is well known that epigenetic modifications may result in abnormal gene expression patterns, contributing to tumor initiation and progression. Therefore, this study aimed to analyze the methylation pattern of the STEAP1 gene in PCa versus non-neoplastic cells. Bisulfite amplicon sequencing of the CpG island at the STEAP1 gene promoter showed a higher methylation level in non-neoplastic PNT1A prostate cells than in human PCa samples. Bioinformatic analysis of the GEO datasets also showed the STEAP1 gene promoter as being demethylated in human PCa, and a negative association with STEAP1 mRNA expression was observed. These results are supported by the treatment of non-neoplastic PNT1A cells with DNMT and HDAC inhibitors, which induced a significant increase in STEAP1 mRNA expression. In addition, the involvement of HDAC in the regulation of STEAP1 mRNA expression was corroborated by a negative association between STEAP1 mRNA expression and HDAC4,5,7 and 9 in human PCa. In conclusion, our work indicates that STEAP1 overexpression in PCa can be driven by the hypomethylation of STEAP1 gene promoter. MDPI 2021-11-17 /pmc/articles/PMC8618799/ /pubmed/34833128 http://dx.doi.org/10.3390/life11111251 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 | Article Rocha, Sandra M. Sousa, Inês Gomes, Inês M. Arinto, Patrícia Costa-Pinheiro, Pedro Coutinho, Eduarda Santos, Cecília R. Jerónimo, Carmen Lemos, Manuel C. Passarinha, Luís A. Socorro, Sílvia Maia, Cláudio J. Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis |
title | Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis |
title_full | Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis |
title_fullStr | Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis |
title_full_unstemmed | Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis |
title_short | Promoter Demethylation Upregulates STEAP1 Gene Expression in Human Prostate Cancer: In Vitro and In Silico Analysis |
title_sort | promoter demethylation upregulates steap1 gene expression in human prostate cancer: in vitro and in silico analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618799/ https://www.ncbi.nlm.nih.gov/pubmed/34833128 http://dx.doi.org/10.3390/life11111251 |
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