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Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization
Prostate cancer is the most frequently diagnosed male visceral cancer and the second leading cause of cancer death in the United States. Standard tests such as prostate-specific antigen (PSA) measurement have poor specificity (33%) resulting in a high number of false positive reports. Consequently t...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910593/ https://www.ncbi.nlm.nih.gov/pubmed/27313791 http://dx.doi.org/10.7150/jca.14645 |
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author | Truong, Quach Justiniano, Irene O. Nocon, Aline L. Soon, Julie T. Wissmueller, Sandra Campbell, Douglas H. Walsh, Bradley J. |
author_facet | Truong, Quach Justiniano, Irene O. Nocon, Aline L. Soon, Julie T. Wissmueller, Sandra Campbell, Douglas H. Walsh, Bradley J. |
author_sort | Truong, Quach |
collection | PubMed |
description | Prostate cancer is the most frequently diagnosed male visceral cancer and the second leading cause of cancer death in the United States. Standard tests such as prostate-specific antigen (PSA) measurement have poor specificity (33%) resulting in a high number of false positive reports. Consequently there is a need for new biomarkers to address this problem. The MIL-38 antibody was first described nearly thirty years ago, however, until now, the identification of the target antigen remained elusive. By a series of molecular techniques and mass spectrometry, the MIL-38 antigen was identified to be the highly glycosylated proteoglycan Glypican-1 (GPC-1). This protein is present in two forms; a membrane bound core protein of 55-60 kDa and secreted soluble forms of 40 kDa and 52 kDa. GPC-1 identification was confirmed by immuno-precipitation, western blots and ELISA. An ELISA platform is currently being developed to assess the levels of GPC-1 in normal, benign prostatic hyperplasia (BPH) and prostate cancer patients to determine whether secreted GPC-1 may represent a clinically relevant biomarker for prostate cancer diagnosis. |
format | Online Article Text |
id | pubmed-4910593 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-49105932016-06-16 Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization Truong, Quach Justiniano, Irene O. Nocon, Aline L. Soon, Julie T. Wissmueller, Sandra Campbell, Douglas H. Walsh, Bradley J. J Cancer Research Paper Prostate cancer is the most frequently diagnosed male visceral cancer and the second leading cause of cancer death in the United States. Standard tests such as prostate-specific antigen (PSA) measurement have poor specificity (33%) resulting in a high number of false positive reports. Consequently there is a need for new biomarkers to address this problem. The MIL-38 antibody was first described nearly thirty years ago, however, until now, the identification of the target antigen remained elusive. By a series of molecular techniques and mass spectrometry, the MIL-38 antigen was identified to be the highly glycosylated proteoglycan Glypican-1 (GPC-1). This protein is present in two forms; a membrane bound core protein of 55-60 kDa and secreted soluble forms of 40 kDa and 52 kDa. GPC-1 identification was confirmed by immuno-precipitation, western blots and ELISA. An ELISA platform is currently being developed to assess the levels of GPC-1 in normal, benign prostatic hyperplasia (BPH) and prostate cancer patients to determine whether secreted GPC-1 may represent a clinically relevant biomarker for prostate cancer diagnosis. Ivyspring International Publisher 2016-05-21 /pmc/articles/PMC4910593/ /pubmed/27313791 http://dx.doi.org/10.7150/jca.14645 Text en © Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions. |
spellingShingle | Research Paper Truong, Quach Justiniano, Irene O. Nocon, Aline L. Soon, Julie T. Wissmueller, Sandra Campbell, Douglas H. Walsh, Bradley J. Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization |
title | Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization |
title_full | Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization |
title_fullStr | Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization |
title_full_unstemmed | Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization |
title_short | Glypican-1 as a Biomarker for Prostate Cancer: Isolation and Characterization |
title_sort | glypican-1 as a biomarker for prostate cancer: isolation and characterization |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4910593/ https://www.ncbi.nlm.nih.gov/pubmed/27313791 http://dx.doi.org/10.7150/jca.14645 |
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