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Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125

The ovarian cancer biomarker CA125 has been extensively investigated over the last 30 years. The knowledge about the exact molecular nature of this protein, however, remains fragmented. This review provides an overview of the structural research regarding CA125, and presents an orthogonal verificati...

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Autores principales: Weiland, Florian, Martin, Karina, Oehler, Martin K., Hoffmann, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431878/
https://www.ncbi.nlm.nih.gov/pubmed/22949880
http://dx.doi.org/10.3390/ijms130810568
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author Weiland, Florian
Martin, Karina
Oehler, Martin K.
Hoffmann, Peter
author_facet Weiland, Florian
Martin, Karina
Oehler, Martin K.
Hoffmann, Peter
author_sort Weiland, Florian
collection PubMed
description The ovarian cancer biomarker CA125 has been extensively investigated over the last 30 years. The knowledge about the exact molecular nature of this protein, however, remains fragmented. This review provides an overview of the structural research regarding CA125, and presents an orthogonal verification method to confirm the identity of this molecule. The need for independent identification of CA125 is exemplified by several reports where mutually exclusive data concerning the existence of isoforms and the glycan moieties is presented. Mass spectrometry can overcome the pitfalls of a single detection/identification method such as antibody probing. Independent verification of CA125 identity in characterization studies will help establish a refined model of its molecular structure that will promote the development of new approaches for diagnosis, prognosis and therapy of ovarian cancer.
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spelling pubmed-34318782012-09-04 Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125 Weiland, Florian Martin, Karina Oehler, Martin K. Hoffmann, Peter Int J Mol Sci Review The ovarian cancer biomarker CA125 has been extensively investigated over the last 30 years. The knowledge about the exact molecular nature of this protein, however, remains fragmented. This review provides an overview of the structural research regarding CA125, and presents an orthogonal verification method to confirm the identity of this molecule. The need for independent identification of CA125 is exemplified by several reports where mutually exclusive data concerning the existence of isoforms and the glycan moieties is presented. Mass spectrometry can overcome the pitfalls of a single detection/identification method such as antibody probing. Independent verification of CA125 identity in characterization studies will help establish a refined model of its molecular structure that will promote the development of new approaches for diagnosis, prognosis and therapy of ovarian cancer. Molecular Diversity Preservation International (MDPI) 2012-08-22 /pmc/articles/PMC3431878/ /pubmed/22949880 http://dx.doi.org/10.3390/ijms130810568 Text en © 2012 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Weiland, Florian
Martin, Karina
Oehler, Martin K.
Hoffmann, Peter
Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125
title Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125
title_full Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125
title_fullStr Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125
title_full_unstemmed Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125
title_short Deciphering the Molecular Nature of Ovarian Cancer Biomarker CA125
title_sort deciphering the molecular nature of ovarian cancer biomarker ca125
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3431878/
https://www.ncbi.nlm.nih.gov/pubmed/22949880
http://dx.doi.org/10.3390/ijms130810568
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