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Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer
INTRODUCTION: Recently, growing evidence indicates that immunoglobulins (Igs) are not only produced by mature B lymphocytes or plasma cells, but also by various normal cells types at immune privileged sites and neoplasm, including breast cancer. However, the association of breast cancer derived IgG...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595271/ https://www.ncbi.nlm.nih.gov/pubmed/23554916 http://dx.doi.org/10.1371/journal.pone.0058706 |
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author | Yang, Baokai Ma, Changchun Chen, Zhengshan Yi, Weining McNutt, Michael A. Wang, Yun Korteweg, Christine Gu, Jiang |
author_facet | Yang, Baokai Ma, Changchun Chen, Zhengshan Yi, Weining McNutt, Michael A. Wang, Yun Korteweg, Christine Gu, Jiang |
author_sort | Yang, Baokai |
collection | PubMed |
description | INTRODUCTION: Recently, growing evidence indicates that immunoglobulins (Igs) are not only produced by mature B lymphocytes or plasma cells, but also by various normal cells types at immune privileged sites and neoplasm, including breast cancer. However, the association of breast cancer derived IgG with genesis and development of the disease has not yet been established. METHODS: In this study we examined the expression of IgG in 186 breast cancers, 20 benign breast lesions and 30 normal breast tissues. Both immunohistochemistry with antibodies to Igκ (immunoglobulin G κ light chain) and Igγ (immunoglobulin G heavy chain) and in situ hybridization with an antisense probe to IgG1 heavy chain constant region gene were performed. Various clinicopathological features were also analyzed. RESULTS: We found that IgG is specifically expressed in human breast cancer cells. Both infiltrating ductal carcinoma and infiltrating lobular carcinoma had significantly greater numbers of Igκ and Igγ positive cancer cells as compared with medullary carcinoma, carcinoma in situ, and benign lesions (all p<0.05). In addition, IgG expression was correlated with breast cancer histological subtypes (p<0.01) and AJCC stages (p<0.05), with more abundance of IgG expression in more malignant histological subtypes or in more advanced stage of the disease. CONCLUSIONS: IgG expression in breast cancer cells is correlated with malignancy and AJCC stages of the cancers. This suggests that breast cancer derived IgG may be associated with genesis, development and prognosis of the cancer. |
format | Online Article Text |
id | pubmed-3595271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35952712013-04-02 Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer Yang, Baokai Ma, Changchun Chen, Zhengshan Yi, Weining McNutt, Michael A. Wang, Yun Korteweg, Christine Gu, Jiang PLoS One Research Article INTRODUCTION: Recently, growing evidence indicates that immunoglobulins (Igs) are not only produced by mature B lymphocytes or plasma cells, but also by various normal cells types at immune privileged sites and neoplasm, including breast cancer. However, the association of breast cancer derived IgG with genesis and development of the disease has not yet been established. METHODS: In this study we examined the expression of IgG in 186 breast cancers, 20 benign breast lesions and 30 normal breast tissues. Both immunohistochemistry with antibodies to Igκ (immunoglobulin G κ light chain) and Igγ (immunoglobulin G heavy chain) and in situ hybridization with an antisense probe to IgG1 heavy chain constant region gene were performed. Various clinicopathological features were also analyzed. RESULTS: We found that IgG is specifically expressed in human breast cancer cells. Both infiltrating ductal carcinoma and infiltrating lobular carcinoma had significantly greater numbers of Igκ and Igγ positive cancer cells as compared with medullary carcinoma, carcinoma in situ, and benign lesions (all p<0.05). In addition, IgG expression was correlated with breast cancer histological subtypes (p<0.01) and AJCC stages (p<0.05), with more abundance of IgG expression in more malignant histological subtypes or in more advanced stage of the disease. CONCLUSIONS: IgG expression in breast cancer cells is correlated with malignancy and AJCC stages of the cancers. This suggests that breast cancer derived IgG may be associated with genesis, development and prognosis of the cancer. Public Library of Science 2013-03-12 /pmc/articles/PMC3595271/ /pubmed/23554916 http://dx.doi.org/10.1371/journal.pone.0058706 Text en © 2013 Yang 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 Yang, Baokai Ma, Changchun Chen, Zhengshan Yi, Weining McNutt, Michael A. Wang, Yun Korteweg, Christine Gu, Jiang Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer |
title | Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer |
title_full | Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer |
title_fullStr | Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer |
title_full_unstemmed | Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer |
title_short | Correlation of Immunoglobulin G Expression and Histological Subtype and Stage in Breast Cancer |
title_sort | correlation of immunoglobulin g expression and histological subtype and stage in breast cancer |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3595271/ https://www.ncbi.nlm.nih.gov/pubmed/23554916 http://dx.doi.org/10.1371/journal.pone.0058706 |
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