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Characterization and clinical validation of MCM2 and TOP2A monoclonal antibodies in the BD ProEx™ C assay: An immunoassay which detects aberrant S-phase induction in cervical tissue.
- Source :
-
Journal of immunological methods [J Immunol Methods] 2017 Mar; Vol. 442, pp. 35-41. Date of Electronic Publication: 2017 Jan 16. - Publication Year :
- 2017
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Abstract
- Background: The Papanicolaou (Pap) screen has been successful in reducing cervical cancer; but exhibits low sensitivity when detecting cervical dysplasia. Use of molecular biomarkers in Pap tests may improve diagnostic accuracy.<br />Design: Monoclonal antibodies to Minichromosome Maintenance Protein 2 (MCM2) and DNA Topoisomerase II α (TOP2A) were selected for use in IHC based on their ability to differentiate normal from diseased cervical tissues in tissue microarrays. Enhanced Green Fluorescent Protein Western blot analysis was used to help identify binding epitopes specific to MCM2 and TOP2A antibody clones. Antibody affinity was determined by solution phase affinity measurement and immunohistochemistry was performed using high affinity MCM2 or TOP2A antibodies on serial histological sections.<br />Results: Antibody clones to MCM2 and TOP2A clones were selected based on their ability to detect over expression in abnormal cervical epithelia. In IHC, MCM2-27C5.6 and MCM2-26H6.19 demonstrated superior staining in abnormal cervical tissue over the MCM2-CRCT2.1 antibody. A combination of MCM2 and TOP2A antibodies showed greater staining when compared to staining with any of the antibodies alone on serial histological sections. Distinct linear epitopes were elucidated for each of the MCM2 and TOP2A clones. Affinity values (Kd) for MCM2 or TOP2A antibodies had a similar range. In a research study, the MCM2 and TOP2A (BD ProEx™ C) antibody cocktail showed increased epithelia staining with increasing dysplasia. The use of BD ProEx™ C in combination with H&E staining enhanced immunohistochemical discrimination of dysplastic and non-dysplastic FFPE cervical tissue specimens.<br />Conclusions: BD ProEx™ C containing MCM2 and TOP2A antibodies showed strong specific nuclear staining that correlated with increased dysplasia and lesion severity. Enhanced performance of the antibodies was linked to their unique topography recognition. BD ProEx™ C incorporates antibodies that enhance detection of CIN2+ cervical disease.<br /> (Copyright © 2017 Elsevier B.V. All rights reserved.)
- Subjects :
- Biopsy
Blotting, Western
Cell Nucleus enzymology
Cell Nucleus immunology
Cell Nucleus pathology
Cervix Uteri enzymology
Cervix Uteri pathology
Epitope Mapping methods
Epitopes
Female
Humans
Poly-ADP-Ribose Binding Proteins
Predictive Value of Tests
Severity of Illness Index
Uterine Cervical Dysplasia enzymology
Uterine Cervical Dysplasia immunology
Uterine Cervical Dysplasia pathology
Uterine Cervical Neoplasms enzymology
Uterine Cervical Neoplasms immunology
Uterine Cervical Neoplasms pathology
Antibodies, Monoclonal immunology
Antigens, Neoplasm immunology
Cervix Uteri immunology
DNA Topoisomerases, Type II immunology
DNA-Binding Proteins immunology
Immunohistochemistry
Minichromosome Maintenance Complex Component 2 immunology
S Phase
Tissue Array Analysis methods
Uterine Cervical Dysplasia diagnosis
Uterine Cervical Neoplasms diagnosis
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7905
- Volume :
- 442
- Database :
- MEDLINE
- Journal :
- Journal of immunological methods
- Publication Type :
- Academic Journal
- Accession number :
- 28093271
- Full Text :
- https://doi.org/10.1016/j.jim.2017.01.002