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A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases

BACKGROUND: The lack of sufficient specificity and sensitivity among conventional cancer biomarkers, such as prostate specific antigen (PSA) for prostate cancer has been widely recognized after several decades of clinical implications. Autoantibodies (autoAb) among others are being extensively inves...

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Autores principales: Xie, Chong, Kim, Hyun J, Haw, Jonathan G, Kalbasi, Anusha, Gardner, Brian K, Li, Gang, Rao, Jianyu, Chia, David, Liong, Monty, Punzalan, Rubio R, Marks, Leonard S, Pantuck, Allan J, de la Taille, Alexandre, Wang, Guomin, Mukouyama, Hideki, Zeng, Gang
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102624/
https://www.ncbi.nlm.nih.gov/pubmed/21504557
http://dx.doi.org/10.1186/1479-5876-9-43
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author Xie, Chong
Kim, Hyun J
Haw, Jonathan G
Kalbasi, Anusha
Gardner, Brian K
Li, Gang
Rao, Jianyu
Chia, David
Liong, Monty
Punzalan, Rubio R
Marks, Leonard S
Pantuck, Allan J
de la Taille, Alexandre
Wang, Guomin
Mukouyama, Hideki
Zeng, Gang
author_facet Xie, Chong
Kim, Hyun J
Haw, Jonathan G
Kalbasi, Anusha
Gardner, Brian K
Li, Gang
Rao, Jianyu
Chia, David
Liong, Monty
Punzalan, Rubio R
Marks, Leonard S
Pantuck, Allan J
de la Taille, Alexandre
Wang, Guomin
Mukouyama, Hideki
Zeng, Gang
author_sort Xie, Chong
collection PubMed
description BACKGROUND: The lack of sufficient specificity and sensitivity among conventional cancer biomarkers, such as prostate specific antigen (PSA) for prostate cancer has been widely recognized after several decades of clinical implications. Autoantibodies (autoAb) among others are being extensively investigated as potential substitute markers, but remain elusive. One major obstacle is the lack of a sensitive and multiplex approach for quantifying autoAb against a large panel of clinically relevant tumor-associated antigens (TAA). METHODS: To circumvent preparation of phage lysates and purification of recombinant proteins, we identified B cell epitopes from a number of previously defined prostate cancer-associated antigens (PCAA). Peptide epitopes from cancer/testis antigen NY-ESO-1, XAGE-1b, SSX-2,4, as well as prostate cancer overexpressed antigen AMACR, p90 autoantigen, and LEDGF were then conjugated with seroMAP microspheres to allow multiplex measurement of autoAb present in serum samples. Moreover, simultaneous quantification of autoAb plus total PSA was achieved in one reaction, and termed the "A+PSA" assay. RESULTS: Peptide epitopes from the above 6 PCAA were identified and confirmed that autoAb against these peptide epitopes reacted specifically with the full-length protein. A pilot study was conducted with the A+PSA assay using pre-surgery sera from 131 biopsy-confirmed prostate cancer patients and 121 benign prostatic hyperplasia and/or prostatitis patients. A logistic regression-based A+PSA index was found to enhance sensitivities and specificities over PSA alone in distinguishing prostate cancer from nonmalignant cases. The A+PSA index also reduced false positive rate and improved the area under a receiver operating characteristic curve. CONCLUSIONS: The A+PSA assay represents a novel platform that integrates autoAb signatures with a conventional cancer biomarker, which may aid in the diagnosis and prognosis of prostate cancer and others.
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spelling pubmed-31026242011-05-27 A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases Xie, Chong Kim, Hyun J Haw, Jonathan G Kalbasi, Anusha Gardner, Brian K Li, Gang Rao, Jianyu Chia, David Liong, Monty Punzalan, Rubio R Marks, Leonard S Pantuck, Allan J de la Taille, Alexandre Wang, Guomin Mukouyama, Hideki Zeng, Gang J Transl Med Research BACKGROUND: The lack of sufficient specificity and sensitivity among conventional cancer biomarkers, such as prostate specific antigen (PSA) for prostate cancer has been widely recognized after several decades of clinical implications. Autoantibodies (autoAb) among others are being extensively investigated as potential substitute markers, but remain elusive. One major obstacle is the lack of a sensitive and multiplex approach for quantifying autoAb against a large panel of clinically relevant tumor-associated antigens (TAA). METHODS: To circumvent preparation of phage lysates and purification of recombinant proteins, we identified B cell epitopes from a number of previously defined prostate cancer-associated antigens (PCAA). Peptide epitopes from cancer/testis antigen NY-ESO-1, XAGE-1b, SSX-2,4, as well as prostate cancer overexpressed antigen AMACR, p90 autoantigen, and LEDGF were then conjugated with seroMAP microspheres to allow multiplex measurement of autoAb present in serum samples. Moreover, simultaneous quantification of autoAb plus total PSA was achieved in one reaction, and termed the "A+PSA" assay. RESULTS: Peptide epitopes from the above 6 PCAA were identified and confirmed that autoAb against these peptide epitopes reacted specifically with the full-length protein. A pilot study was conducted with the A+PSA assay using pre-surgery sera from 131 biopsy-confirmed prostate cancer patients and 121 benign prostatic hyperplasia and/or prostatitis patients. A logistic regression-based A+PSA index was found to enhance sensitivities and specificities over PSA alone in distinguishing prostate cancer from nonmalignant cases. The A+PSA index also reduced false positive rate and improved the area under a receiver operating characteristic curve. CONCLUSIONS: The A+PSA assay represents a novel platform that integrates autoAb signatures with a conventional cancer biomarker, which may aid in the diagnosis and prognosis of prostate cancer and others. BioMed Central 2011-04-19 /pmc/articles/PMC3102624/ /pubmed/21504557 http://dx.doi.org/10.1186/1479-5876-9-43 Text en Copyright ©2011 Xie et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Xie, Chong
Kim, Hyun J
Haw, Jonathan G
Kalbasi, Anusha
Gardner, Brian K
Li, Gang
Rao, Jianyu
Chia, David
Liong, Monty
Punzalan, Rubio R
Marks, Leonard S
Pantuck, Allan J
de la Taille, Alexandre
Wang, Guomin
Mukouyama, Hideki
Zeng, Gang
A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases
title A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases
title_full A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases
title_fullStr A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases
title_full_unstemmed A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases
title_short A novel multiplex assay combining autoantibodies plus PSA has potential implications for classification of prostate cancer from non-malignant cases
title_sort novel multiplex assay combining autoantibodies plus psa has potential implications for classification of prostate cancer from non-malignant cases
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3102624/
https://www.ncbi.nlm.nih.gov/pubmed/21504557
http://dx.doi.org/10.1186/1479-5876-9-43
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