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Plasma biomarker proteins for detection of human growth hormone administration in athletes
Human growth hormone (GH) is a naturally occurring hormone secreted by the pituitary gland with anabolic and growth-promoting activities. Since an increased availability of recombinant GH (rGH) for the treatment of GH-deficient patients, GH has been abused in sports and it is prohibited. “GH-isoform...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577294/ https://www.ncbi.nlm.nih.gov/pubmed/28855568 http://dx.doi.org/10.1038/s41598-017-09968-7 |
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author | Tan, Sock-Hwee Lee, Albert Pascovici, Dana Care, Natasha Birzniece, Vita Ho, Ken Molloy, Mark P. Khan, Alamgir |
author_facet | Tan, Sock-Hwee Lee, Albert Pascovici, Dana Care, Natasha Birzniece, Vita Ho, Ken Molloy, Mark P. Khan, Alamgir |
author_sort | Tan, Sock-Hwee |
collection | PubMed |
description | Human growth hormone (GH) is a naturally occurring hormone secreted by the pituitary gland with anabolic and growth-promoting activities. Since an increased availability of recombinant GH (rGH) for the treatment of GH-deficient patients, GH has been abused in sports and it is prohibited. “GH-isoform” and “biomarkers” tests are currently available for detection of GH abuse in sports, however both methods suffer from shortcomings. Here, we report on a proteomic approach to search for novel protein biomarkers associated with rGH administration in non-elite athletes. In this study, participants received either placebo or rGH for 8 weeks, and were followed over a 6-week washout period. We used 2-D DIGE and iTRAQ LC-MS/MS analyses to expose rGH-dependent marker proteins. Eight rGH-dependent plasma proteins namely apolipoproptein-L1, alpha-HS-glycoprotein, vitamin D-binding protein, afamin, insulin-like growth factor-binding protein-3, insulin-like growth factor-binding protein-ALS, lumican and extracellular matrix proteins 1 were identified. Apolipoprotein L1 and alpha-HS-glycoprotein were validated by Western blots to confirm their identities and expression patterns in rGH- and placebo-treated subject cohorts. Independent confirmation of these putative GH-responsive biomarkers would be of value for clinical practices and may have sports anti-doping utility. |
format | Online Article Text |
id | pubmed-5577294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55772942017-09-06 Plasma biomarker proteins for detection of human growth hormone administration in athletes Tan, Sock-Hwee Lee, Albert Pascovici, Dana Care, Natasha Birzniece, Vita Ho, Ken Molloy, Mark P. Khan, Alamgir Sci Rep Article Human growth hormone (GH) is a naturally occurring hormone secreted by the pituitary gland with anabolic and growth-promoting activities. Since an increased availability of recombinant GH (rGH) for the treatment of GH-deficient patients, GH has been abused in sports and it is prohibited. “GH-isoform” and “biomarkers” tests are currently available for detection of GH abuse in sports, however both methods suffer from shortcomings. Here, we report on a proteomic approach to search for novel protein biomarkers associated with rGH administration in non-elite athletes. In this study, participants received either placebo or rGH for 8 weeks, and were followed over a 6-week washout period. We used 2-D DIGE and iTRAQ LC-MS/MS analyses to expose rGH-dependent marker proteins. Eight rGH-dependent plasma proteins namely apolipoproptein-L1, alpha-HS-glycoprotein, vitamin D-binding protein, afamin, insulin-like growth factor-binding protein-3, insulin-like growth factor-binding protein-ALS, lumican and extracellular matrix proteins 1 were identified. Apolipoprotein L1 and alpha-HS-glycoprotein were validated by Western blots to confirm their identities and expression patterns in rGH- and placebo-treated subject cohorts. Independent confirmation of these putative GH-responsive biomarkers would be of value for clinical practices and may have sports anti-doping utility. Nature Publishing Group UK 2017-08-30 /pmc/articles/PMC5577294/ /pubmed/28855568 http://dx.doi.org/10.1038/s41598-017-09968-7 Text en © The Author(s) 2017 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Tan, Sock-Hwee Lee, Albert Pascovici, Dana Care, Natasha Birzniece, Vita Ho, Ken Molloy, Mark P. Khan, Alamgir Plasma biomarker proteins for detection of human growth hormone administration in athletes |
title | Plasma biomarker proteins for detection of human growth hormone administration in athletes |
title_full | Plasma biomarker proteins for detection of human growth hormone administration in athletes |
title_fullStr | Plasma biomarker proteins for detection of human growth hormone administration in athletes |
title_full_unstemmed | Plasma biomarker proteins for detection of human growth hormone administration in athletes |
title_short | Plasma biomarker proteins for detection of human growth hormone administration in athletes |
title_sort | plasma biomarker proteins for detection of human growth hormone administration in athletes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577294/ https://www.ncbi.nlm.nih.gov/pubmed/28855568 http://dx.doi.org/10.1038/s41598-017-09968-7 |
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