Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study

Background: Periprostatic adipose tissue (PPAT) has been recognized to associate with prostate cancer (PCa) aggressiveness and progression. Here, we sought to investigate whether excess adiposity modulates the methylome of PPAT in PCa patients. DNA methylation profiling was performed in PPAT from ob...

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Autores: Cheng, Y. (Yan)|||/items/17f91592-112b-4f6d-8251-fb09d1dca92e, Monteiro, C. (Cátia)|||/items/66830b3f-8ce5-4adb-b982-5528a56b6d85, Matos, A. (Andreia)|||/items/e73d2e40-d96d-4ad5-8374-cfc9f5bae71e, You, J. (Jiaying)|||/items/28d9cd0c-7420-4d18-8ac9-3e634c681bc7, Fraga, A. (Avelino)|||/items/f0c31cc8-d4b8-49ff-b4fd-c0b540c475e3, Pereira, C. (Carina)|||/items/f0b8f462-5a63-4fba-af6f-fcaa489d6d2d, Catalán-Goñi, V. (Victoria)|||/items/9a5a055c-323a-4b41-800f-65abf7f22c79, Rodriguez, A. (Amaia)|||/items/50976a5f-9842-47f1-8a9c-508e59996427, Gomez-Ambrosi, J. (Javier)|||/items/21d09997-940a-45f7-9b4b-0a9f64b2ed8e, Frühbeck, G. (Gema)|||/items/7f0b1f72-bc91-4ab0-a3fd-21e9a3fb663b, Ribeiro, R. (Ricardo)|||/items/95aafc4b-5ad7-423d-bba2-fc4cb0710829, Hu, P. (Pingzhao)|||/items/03ba1c6a-a254-4487-b59c-eb41b17b1dba
Tipo de recurso: artículo
Fecha de publicación:2018
País:España
Institución:Universidad de Navarra
Repositorio:Dadun. Depósito Académico Digital de la Universidad de Navarra
Idioma:inglés
OAI Identifier:oai:dadun.unav.edu:10171/64841
Acceso en línea:https://hdl.handle.net/10171/64841
Access Level:acceso abierto
Palabra clave:DNA methylation
Periprostatic adipose tissue
Obesity
Prostate cancer
Microenvironment
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spelling Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot studyCheng, Y. (Yan)|||/items/17f91592-112b-4f6d-8251-fb09d1dca92eMonteiro, C. (Cátia)|||/items/66830b3f-8ce5-4adb-b982-5528a56b6d85Matos, A. (Andreia)|||/items/e73d2e40-d96d-4ad5-8374-cfc9f5bae71eYou, J. (Jiaying)|||/items/28d9cd0c-7420-4d18-8ac9-3e634c681bc7Fraga, A. (Avelino)|||/items/f0c31cc8-d4b8-49ff-b4fd-c0b540c475e3Pereira, C. (Carina)|||/items/f0b8f462-5a63-4fba-af6f-fcaa489d6d2dCatalán-Goñi, V. (Victoria)|||/items/9a5a055c-323a-4b41-800f-65abf7f22c79Rodriguez, A. (Amaia)|||/items/50976a5f-9842-47f1-8a9c-508e59996427Gomez-Ambrosi, J. (Javier)|||/items/21d09997-940a-45f7-9b4b-0a9f64b2ed8eFrühbeck, G. (Gema)|||/items/7f0b1f72-bc91-4ab0-a3fd-21e9a3fb663bRibeiro, R. (Ricardo)|||/items/95aafc4b-5ad7-423d-bba2-fc4cb0710829Hu, P. (Pingzhao)|||/items/03ba1c6a-a254-4487-b59c-eb41b17b1dbaDNA methylationPeriprostatic adipose tissueObesityProstate cancerMicroenvironmentBackground: Periprostatic adipose tissue (PPAT) has been recognized to associate with prostate cancer (PCa) aggressiveness and progression. Here, we sought to investigate whether excess adiposity modulates the methylome of PPAT in PCa patients. DNA methylation profiling was performed in PPAT from obese/overweight (OB/OW, BMI > 25 kg m−2 ) and normal weight (NW, BMI < 25 kg m−2 ) PCa patients. Significant differences in methylated CpGs between OB/OW and NW groups were inferred by statistical modeling. Results: Five thousand five hundred twenty-six differentially methylated CpGs were identified between OB/OW and NW PCa patients with 90.2% hypermethylated. Four hundred eighty-three of these CpGs were found to be located at both promoters and CpG islands, whereas the representing 412 genes were found to be involved in pluripotency of stem cells, fatty acid metabolism, and many other biological processes; 14 of these genes, particularly FADS1, MOGAT1, and PCYT2, with promoter hypermethylation presented with significantly decreased gene expression in matched samples. Additionally, 38 genes were correlated with antigen processing and presentation of endogenous antigen via MHC class I, which might result in fatty acid accumulation in PPAT and tumor immune evasion. Conclusions: Results showed that the whole epigenome methylation profiles of PPAT were significantly different in OB/OW compared to normal weight PCa patients. The epigenetic variation associated with excess adiposity likely resulted in altered lipid metabolism and immune dysregulation, contributing towards unfavorable PCa microenvironment, thus warranting further validation studies in larger samples.BioMed CentralDadun. Depósito Académico Digital Universidad de Navarra20222022-12-1420182018-01-0120182018-01-01journal articlehttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10171/64841reponame:Dadun. Depósito Académico Digital de la Universidad de Navarrainstname:Universidad de NavarraInglésengopen accesshttp://purl.org/coar/access_right/c_abf2info:eu-repo/semantics/openAccessoai:dadun.unav.edu:10171/648412026-06-21T12:47:57Z
dc.title.none.fl_str_mv Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
title Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
spellingShingle Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
Cheng, Y. (Yan)|||/items/17f91592-112b-4f6d-8251-fb09d1dca92e
DNA methylation
Periprostatic adipose tissue
Obesity
Prostate cancer
Microenvironment
title_short Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
title_full Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
title_fullStr Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
title_full_unstemmed Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
title_sort Epigenome-wide DNA methylation profiling of periprostatic adipose tissue in prostate cancer patients with excess adiposity-a pilot study
dc.creator.none.fl_str_mv Cheng, Y. (Yan)|||/items/17f91592-112b-4f6d-8251-fb09d1dca92e
Monteiro, C. (Cátia)|||/items/66830b3f-8ce5-4adb-b982-5528a56b6d85
Matos, A. (Andreia)|||/items/e73d2e40-d96d-4ad5-8374-cfc9f5bae71e
You, J. (Jiaying)|||/items/28d9cd0c-7420-4d18-8ac9-3e634c681bc7
Fraga, A. (Avelino)|||/items/f0c31cc8-d4b8-49ff-b4fd-c0b540c475e3
Pereira, C. (Carina)|||/items/f0b8f462-5a63-4fba-af6f-fcaa489d6d2d
Catalán-Goñi, V. (Victoria)|||/items/9a5a055c-323a-4b41-800f-65abf7f22c79
Rodriguez, A. (Amaia)|||/items/50976a5f-9842-47f1-8a9c-508e59996427
Gomez-Ambrosi, J. (Javier)|||/items/21d09997-940a-45f7-9b4b-0a9f64b2ed8e
Frühbeck, G. (Gema)|||/items/7f0b1f72-bc91-4ab0-a3fd-21e9a3fb663b
Ribeiro, R. (Ricardo)|||/items/95aafc4b-5ad7-423d-bba2-fc4cb0710829
Hu, P. (Pingzhao)|||/items/03ba1c6a-a254-4487-b59c-eb41b17b1dba
author Cheng, Y. (Yan)|||/items/17f91592-112b-4f6d-8251-fb09d1dca92e
author_facet Cheng, Y. (Yan)|||/items/17f91592-112b-4f6d-8251-fb09d1dca92e
Monteiro, C. (Cátia)|||/items/66830b3f-8ce5-4adb-b982-5528a56b6d85
Matos, A. (Andreia)|||/items/e73d2e40-d96d-4ad5-8374-cfc9f5bae71e
You, J. (Jiaying)|||/items/28d9cd0c-7420-4d18-8ac9-3e634c681bc7
Fraga, A. (Avelino)|||/items/f0c31cc8-d4b8-49ff-b4fd-c0b540c475e3
Pereira, C. (Carina)|||/items/f0b8f462-5a63-4fba-af6f-fcaa489d6d2d
Catalán-Goñi, V. (Victoria)|||/items/9a5a055c-323a-4b41-800f-65abf7f22c79
Rodriguez, A. (Amaia)|||/items/50976a5f-9842-47f1-8a9c-508e59996427
Gomez-Ambrosi, J. (Javier)|||/items/21d09997-940a-45f7-9b4b-0a9f64b2ed8e
Frühbeck, G. (Gema)|||/items/7f0b1f72-bc91-4ab0-a3fd-21e9a3fb663b
Ribeiro, R. (Ricardo)|||/items/95aafc4b-5ad7-423d-bba2-fc4cb0710829
Hu, P. (Pingzhao)|||/items/03ba1c6a-a254-4487-b59c-eb41b17b1dba
author_role author
author2 Monteiro, C. (Cátia)|||/items/66830b3f-8ce5-4adb-b982-5528a56b6d85
Matos, A. (Andreia)|||/items/e73d2e40-d96d-4ad5-8374-cfc9f5bae71e
You, J. (Jiaying)|||/items/28d9cd0c-7420-4d18-8ac9-3e634c681bc7
Fraga, A. (Avelino)|||/items/f0c31cc8-d4b8-49ff-b4fd-c0b540c475e3
Pereira, C. (Carina)|||/items/f0b8f462-5a63-4fba-af6f-fcaa489d6d2d
Catalán-Goñi, V. (Victoria)|||/items/9a5a055c-323a-4b41-800f-65abf7f22c79
Rodriguez, A. (Amaia)|||/items/50976a5f-9842-47f1-8a9c-508e59996427
Gomez-Ambrosi, J. (Javier)|||/items/21d09997-940a-45f7-9b4b-0a9f64b2ed8e
Frühbeck, G. (Gema)|||/items/7f0b1f72-bc91-4ab0-a3fd-21e9a3fb663b
Ribeiro, R. (Ricardo)|||/items/95aafc4b-5ad7-423d-bba2-fc4cb0710829
Hu, P. (Pingzhao)|||/items/03ba1c6a-a254-4487-b59c-eb41b17b1dba
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Dadun. Depósito Académico Digital Universidad de Navarra
dc.subject.none.fl_str_mv DNA methylation
Periprostatic adipose tissue
Obesity
Prostate cancer
Microenvironment
topic DNA methylation
Periprostatic adipose tissue
Obesity
Prostate cancer
Microenvironment
description Background: Periprostatic adipose tissue (PPAT) has been recognized to associate with prostate cancer (PCa) aggressiveness and progression. Here, we sought to investigate whether excess adiposity modulates the methylome of PPAT in PCa patients. DNA methylation profiling was performed in PPAT from obese/overweight (OB/OW, BMI > 25 kg m−2 ) and normal weight (NW, BMI < 25 kg m−2 ) PCa patients. Significant differences in methylated CpGs between OB/OW and NW groups were inferred by statistical modeling. Results: Five thousand five hundred twenty-six differentially methylated CpGs were identified between OB/OW and NW PCa patients with 90.2% hypermethylated. Four hundred eighty-three of these CpGs were found to be located at both promoters and CpG islands, whereas the representing 412 genes were found to be involved in pluripotency of stem cells, fatty acid metabolism, and many other biological processes; 14 of these genes, particularly FADS1, MOGAT1, and PCYT2, with promoter hypermethylation presented with significantly decreased gene expression in matched samples. Additionally, 38 genes were correlated with antigen processing and presentation of endogenous antigen via MHC class I, which might result in fatty acid accumulation in PPAT and tumor immune evasion. Conclusions: Results showed that the whole epigenome methylation profiles of PPAT were significantly different in OB/OW compared to normal weight PCa patients. The epigenetic variation associated with excess adiposity likely resulted in altered lipid metabolism and immune dysregulation, contributing towards unfavorable PCa microenvironment, thus warranting further validation studies in larger samples.
publishDate 2018
dc.date.none.fl_str_mv 2018
2018-01-01
2018
2018-01-01
2022
2022-12-14
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/10171/64841
url https://hdl.handle.net/10171/64841
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv BioMed Central
publisher.none.fl_str_mv BioMed Central
dc.source.none.fl_str_mv reponame:Dadun. Depósito Académico Digital de la Universidad de Navarra
instname:Universidad de Navarra
instname_str Universidad de Navarra
reponame_str Dadun. Depósito Académico Digital de la Universidad de Navarra
collection Dadun. Depósito Académico Digital de la Universidad de Navarra
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repository.mail.fl_str_mv
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