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Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer

The prostate is surrounded by periprostatic adipose tissue (PPAT), the thickness of which has been associated with more aggressive prostate cancer (PCa). There are limited data regarding the functional characteristics of PPAT, how it compares to subcutaneous adipose tissue (SAT), and whether in a se...

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Autores principales: Miladinovic, Dushan, Cusick, Thomas, Mahon, Kate L., Haynes, Anne-Maree, Cortie, Colin H., Meyer, Barbara J., Stricker, Phillip D., Wittert, Gary A., Butler, Lisa M., Horvath, Lisa G., Hoy, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352157/
https://www.ncbi.nlm.nih.gov/pubmed/32481537
http://dx.doi.org/10.3390/cancers12061385
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author Miladinovic, Dushan
Cusick, Thomas
Mahon, Kate L.
Haynes, Anne-Maree
Cortie, Colin H.
Meyer, Barbara J.
Stricker, Phillip D.
Wittert, Gary A.
Butler, Lisa M.
Horvath, Lisa G.
Hoy, Andrew J.
author_facet Miladinovic, Dushan
Cusick, Thomas
Mahon, Kate L.
Haynes, Anne-Maree
Cortie, Colin H.
Meyer, Barbara J.
Stricker, Phillip D.
Wittert, Gary A.
Butler, Lisa M.
Horvath, Lisa G.
Hoy, Andrew J.
author_sort Miladinovic, Dushan
collection PubMed
description The prostate is surrounded by periprostatic adipose tissue (PPAT), the thickness of which has been associated with more aggressive prostate cancer (PCa). There are limited data regarding the functional characteristics of PPAT, how it compares to subcutaneous adipose tissue (SAT), and whether in a setting of localized PCa, these traits are altered by obesity or disease aggressiveness. PPAT and SAT were collected from 60 men (age: 42–78 years, BMI: 21.3–35.6 kg/m(2)) undergoing total prostatectomy for PCa. Compared to SAT, adipocytes in PPAT were smaller, had the same basal rates of fatty acid release (lipolysis) yet released less polyunsaturated fatty acid species, and were more sensitive to isoproterenol-stimulated lipolysis. Basal lipolysis of PPAT was increased in men diagnosed with less aggressive PCa (Gleason score (GS) ≤ 3 + 4) compared to men with more aggressive PCa (GS ≥ 4 + 3) but no other measured adipocyte parameters related to PCa aggressiveness. Likewise, there was no difference in PPAT lipid biology between lean and obese men. In conclusion, lipid biological features of PPAT do differ from SAT; however, we did not observe any meaningful difference in ex vivo PPAT biology that is associated with PCa aggressiveness or obesity. As such, our findings do not support a relationship between altered PCa behavior in obese men and the metabolic reprogramming of PPAT.
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spelling pubmed-73521572020-07-15 Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer Miladinovic, Dushan Cusick, Thomas Mahon, Kate L. Haynes, Anne-Maree Cortie, Colin H. Meyer, Barbara J. Stricker, Phillip D. Wittert, Gary A. Butler, Lisa M. Horvath, Lisa G. Hoy, Andrew J. Cancers (Basel) Article The prostate is surrounded by periprostatic adipose tissue (PPAT), the thickness of which has been associated with more aggressive prostate cancer (PCa). There are limited data regarding the functional characteristics of PPAT, how it compares to subcutaneous adipose tissue (SAT), and whether in a setting of localized PCa, these traits are altered by obesity or disease aggressiveness. PPAT and SAT were collected from 60 men (age: 42–78 years, BMI: 21.3–35.6 kg/m(2)) undergoing total prostatectomy for PCa. Compared to SAT, adipocytes in PPAT were smaller, had the same basal rates of fatty acid release (lipolysis) yet released less polyunsaturated fatty acid species, and were more sensitive to isoproterenol-stimulated lipolysis. Basal lipolysis of PPAT was increased in men diagnosed with less aggressive PCa (Gleason score (GS) ≤ 3 + 4) compared to men with more aggressive PCa (GS ≥ 4 + 3) but no other measured adipocyte parameters related to PCa aggressiveness. Likewise, there was no difference in PPAT lipid biology between lean and obese men. In conclusion, lipid biological features of PPAT do differ from SAT; however, we did not observe any meaningful difference in ex vivo PPAT biology that is associated with PCa aggressiveness or obesity. As such, our findings do not support a relationship between altered PCa behavior in obese men and the metabolic reprogramming of PPAT. MDPI 2020-05-28 /pmc/articles/PMC7352157/ /pubmed/32481537 http://dx.doi.org/10.3390/cancers12061385 Text en © 2020 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Miladinovic, Dushan
Cusick, Thomas
Mahon, Kate L.
Haynes, Anne-Maree
Cortie, Colin H.
Meyer, Barbara J.
Stricker, Phillip D.
Wittert, Gary A.
Butler, Lisa M.
Horvath, Lisa G.
Hoy, Andrew J.
Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer
title Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer
title_full Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer
title_fullStr Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer
title_full_unstemmed Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer
title_short Assessment of Periprostatic and Subcutaneous Adipose Tissue Lipolysis and Adipocyte Size from Men with Localized Prostate Cancer
title_sort assessment of periprostatic and subcutaneous adipose tissue lipolysis and adipocyte size from men with localized prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7352157/
https://www.ncbi.nlm.nih.gov/pubmed/32481537
http://dx.doi.org/10.3390/cancers12061385
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