Cargando…

Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity

Immunohistochemistry is one of the most suitable methods for the detection of intratumoral aromatase in order to identify patients who may respond to aromatase inhibitor therapy in hormone-dependent breast cancer. Previous studies showed statistically significant correlation between results of immnu...

Descripción completa

Detalles Bibliográficos
Autores principales: Hong, Yanyan, Li, Hongzhi, Ye, Jingjing, Miki, Yasuhiro, Yuan, Yate-Ching, Sasano, Hironobu, Evans, Dean B., Chen, Shiuan
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778552/
https://www.ncbi.nlm.nih.gov/pubmed/19956630
http://dx.doi.org/10.1371/journal.pone.0008050
_version_ 1782174265695535104
author Hong, Yanyan
Li, Hongzhi
Ye, Jingjing
Miki, Yasuhiro
Yuan, Yate-Ching
Sasano, Hironobu
Evans, Dean B.
Chen, Shiuan
author_facet Hong, Yanyan
Li, Hongzhi
Ye, Jingjing
Miki, Yasuhiro
Yuan, Yate-Ching
Sasano, Hironobu
Evans, Dean B.
Chen, Shiuan
author_sort Hong, Yanyan
collection PubMed
description Immunohistochemistry is one of the most suitable methods for the detection of intratumoral aromatase in order to identify patients who may respond to aromatase inhibitor therapy in hormone-dependent breast cancer. Previous studies showed statistically significant correlation between results of immnuohistochemistry and biochemical analysis in carcinoma components stained by aromatase monoclonal antibody 677. In this study, determination of the antigenic peptides recognized by aromatase antibodies through epitope mapping, combined with the new knowledge on aromatase-reductase interaction, provide insights for understanding various immunostaining patterns using different aromatase antibodies. Our studies on aromatase-reductase interaction also provided critical information on how aromatase and reductase interact with each other on the endoplasmic reticulum membrane, and identified key residues, including K108 of aromatase, that are involved in the interaction with reductase. Through epitope mapping and taking into consideration the interference with aromatase immunohistochemical staining by NADPH-cytochrome P450 reductase, we demonstrated that monoclonal antibody 677 is a suitable antibody for an assessment of intratumoral aromatase activity in breast cancer patients for making clinical management decisions. These results also provide valuable information to identify new aromatase antibodies for immunohistochemical diagnosis of hormone-dependent breast cancer in future.
format Text
id pubmed-2778552
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-27785522009-12-03 Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity Hong, Yanyan Li, Hongzhi Ye, Jingjing Miki, Yasuhiro Yuan, Yate-Ching Sasano, Hironobu Evans, Dean B. Chen, Shiuan PLoS One Research Article Immunohistochemistry is one of the most suitable methods for the detection of intratumoral aromatase in order to identify patients who may respond to aromatase inhibitor therapy in hormone-dependent breast cancer. Previous studies showed statistically significant correlation between results of immnuohistochemistry and biochemical analysis in carcinoma components stained by aromatase monoclonal antibody 677. In this study, determination of the antigenic peptides recognized by aromatase antibodies through epitope mapping, combined with the new knowledge on aromatase-reductase interaction, provide insights for understanding various immunostaining patterns using different aromatase antibodies. Our studies on aromatase-reductase interaction also provided critical information on how aromatase and reductase interact with each other on the endoplasmic reticulum membrane, and identified key residues, including K108 of aromatase, that are involved in the interaction with reductase. Through epitope mapping and taking into consideration the interference with aromatase immunohistochemical staining by NADPH-cytochrome P450 reductase, we demonstrated that monoclonal antibody 677 is a suitable antibody for an assessment of intratumoral aromatase activity in breast cancer patients for making clinical management decisions. These results also provide valuable information to identify new aromatase antibodies for immunohistochemical diagnosis of hormone-dependent breast cancer in future. Public Library of Science 2009-11-30 /pmc/articles/PMC2778552/ /pubmed/19956630 http://dx.doi.org/10.1371/journal.pone.0008050 Text en Hong et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hong, Yanyan
Li, Hongzhi
Ye, Jingjing
Miki, Yasuhiro
Yuan, Yate-Ching
Sasano, Hironobu
Evans, Dean B.
Chen, Shiuan
Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity
title Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity
title_full Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity
title_fullStr Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity
title_full_unstemmed Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity
title_short Epitope Characterization of an Aromatase Monoclonal Antibody Suitable for the Assessment of Intratumoral Aromatase Activity
title_sort epitope characterization of an aromatase monoclonal antibody suitable for the assessment of intratumoral aromatase activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778552/
https://www.ncbi.nlm.nih.gov/pubmed/19956630
http://dx.doi.org/10.1371/journal.pone.0008050
work_keys_str_mv AT hongyanyan epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT lihongzhi epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT yejingjing epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT mikiyasuhiro epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT yuanyateching epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT sasanohironobu epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT evansdeanb epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity
AT chenshiuan epitopecharacterizationofanaromatasemonoclonalantibodysuitablefortheassessmentofintratumoralaromataseactivity