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Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures()
BACKGROUND: Due to the low specificity of the prostate-specific antigen (PSA) assay and a high false positive rate, a large number of prostate cancer (PCA) biopsies are performed unnecessarily. Consequently, there is a need for new biomarkers that can identify PCA at any stage of progression while l...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415116/ https://www.ncbi.nlm.nih.gov/pubmed/25926076 http://dx.doi.org/10.1016/j.tranon.2015.02.003 |
_version_ | 1782369023455920128 |
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author | Schipper, Matthew Wang, George Giles, Nick Ohrnberger, Jeanne |
author_facet | Schipper, Matthew Wang, George Giles, Nick Ohrnberger, Jeanne |
author_sort | Schipper, Matthew |
collection | PubMed |
description | BACKGROUND: Due to the low specificity of the prostate-specific antigen (PSA) assay and a high false positive rate, a large number of prostate cancer (PCA) biopsies are performed unnecessarily. Consequently, there is a need for new biomarkers that can identify PCA at any stage of progression while limiting the number of false positives. The use of autoantibody signature–developed biomarkers has proven to be an effective method to solve this problem. RESULTS: Using T7 phage–peptide detection, we identified a panel of eight biomarkers for PCA on a training set. The estimated receiver-operating characteristic (ROC) curve had an area under the ROC curve of 0.69 when applied to the validation set. Spearman correlations were high, within 0.7 to 0.9, indicating that the biomarkers have a degree of inter-relatedness. The identified biomarkers play a role in processes such as androgen response regulation and cellular structural integrity and are proteins that are thought to play a role in prostate tumorigenesis. CONCLUSIONS: Autoantibodies against PCA can be developed as biomarkers for detecting PCA. The scores from the algorithm developed here can be used to indicate a relative high or low risk of PCA, particularly for patients with intermediate (4.0 to 10 ng/ml) PSA levels. Since most commercially available assays test for PSA or have a PSA component, this novel approach has the potential to improve diagnosis of PCA using a biologic measure independent of PSA. |
format | Online Article Text |
id | pubmed-4415116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-44151162015-05-04 Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() Schipper, Matthew Wang, George Giles, Nick Ohrnberger, Jeanne Transl Oncol Article BACKGROUND: Due to the low specificity of the prostate-specific antigen (PSA) assay and a high false positive rate, a large number of prostate cancer (PCA) biopsies are performed unnecessarily. Consequently, there is a need for new biomarkers that can identify PCA at any stage of progression while limiting the number of false positives. The use of autoantibody signature–developed biomarkers has proven to be an effective method to solve this problem. RESULTS: Using T7 phage–peptide detection, we identified a panel of eight biomarkers for PCA on a training set. The estimated receiver-operating characteristic (ROC) curve had an area under the ROC curve of 0.69 when applied to the validation set. Spearman correlations were high, within 0.7 to 0.9, indicating that the biomarkers have a degree of inter-relatedness. The identified biomarkers play a role in processes such as androgen response regulation and cellular structural integrity and are proteins that are thought to play a role in prostate tumorigenesis. CONCLUSIONS: Autoantibodies against PCA can be developed as biomarkers for detecting PCA. The scores from the algorithm developed here can be used to indicate a relative high or low risk of PCA, particularly for patients with intermediate (4.0 to 10 ng/ml) PSA levels. Since most commercially available assays test for PSA or have a PSA component, this novel approach has the potential to improve diagnosis of PCA using a biologic measure independent of PSA. Neoplasia Press 2015-04-26 /pmc/articles/PMC4415116/ /pubmed/25926076 http://dx.doi.org/10.1016/j.tranon.2015.02.003 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Schipper, Matthew Wang, George Giles, Nick Ohrnberger, Jeanne Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() |
title | Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() |
title_full | Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() |
title_fullStr | Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() |
title_full_unstemmed | Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() |
title_short | Novel Prostate Cancer Biomarkers Derived from Autoantibody Signatures() |
title_sort | novel prostate cancer biomarkers derived from autoantibody signatures() |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4415116/ https://www.ncbi.nlm.nih.gov/pubmed/25926076 http://dx.doi.org/10.1016/j.tranon.2015.02.003 |
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