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Analysis of the cellular centrosome in fine-needle aspirations of the breast

BACKGROUND: The purpose of the present investigation is to determine whether centrosome amplifications are present in breast tumor cells, whether there are differences of centrosome amplification between benign breast lesions and breast carcinomas, and whether centrosomal analysis can be of value in...

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Autores principales: Guo, Hui-qin, Gao, Meixia, Ma, Jinfang, Xiao, Ting, Zhao, Lin-lin, Gao, Yanning, Pan, Qin-jing
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206724/
https://www.ncbi.nlm.nih.gov/pubmed/17662154
http://dx.doi.org/10.1186/bcr1752
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author Guo, Hui-qin
Gao, Meixia
Ma, Jinfang
Xiao, Ting
Zhao, Lin-lin
Gao, Yanning
Pan, Qin-jing
author_facet Guo, Hui-qin
Gao, Meixia
Ma, Jinfang
Xiao, Ting
Zhao, Lin-lin
Gao, Yanning
Pan, Qin-jing
author_sort Guo, Hui-qin
collection PubMed
description BACKGROUND: The purpose of the present investigation is to determine whether centrosome amplifications are present in breast tumor cells, whether there are differences of centrosome amplification between benign breast lesions and breast carcinomas, and whether centrosomal analysis can be of value in the diagnosis and prognosis of breast carcinoma. METHODS: Using immunofluorescence analysis with an antibody against γ-tubulin, we analyzed centrosome abnormalities in fine-needle aspirations of 100 breast lesions (25 cases with benign lesions and 75 cases with carcinomas). RESULTS: We found that centrosome amplifications, including numerical centrosome amplification and structural centrosome amplification, were present in most breast tumors. Cells with numerical centrosome amplification were found in 23 of 25 benign lesions, and in all 75 cases of breast carcinomas. Cells with structural centrosome amplification were found in three of 25 benign lesions, and in 69 of 75 breast carcinomas. The breast carcinomas showed a mean percentage of cells with numerical centrosome amplification of 4.86% and a mean percentage of cells with structural centrosome amplification of 3.98%. These percentages were significantly higher than those in benign lesions, with a numerical centrosome amplification of 2.77% and a structural centrosome amplification of 0.10%. Furthermore, the mean percentage of cells with structural centrosome amplification was significantly associated with HER2/neu overexpression (P < 0.05) and with negative estrogen receptor status (P < 0.05), and had a borderline association with negative progesterone receptor status (P = 0.056) in breast carcinomas. CONCLUSION: Structural centrosome amplification may bear a close relationship with breast carcinoma and may be a potential biomarker for diagnosis and prognosis of breast carcinoma.
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spelling pubmed-22067242008-01-19 Analysis of the cellular centrosome in fine-needle aspirations of the breast Guo, Hui-qin Gao, Meixia Ma, Jinfang Xiao, Ting Zhao, Lin-lin Gao, Yanning Pan, Qin-jing Breast Cancer Res Research Article BACKGROUND: The purpose of the present investigation is to determine whether centrosome amplifications are present in breast tumor cells, whether there are differences of centrosome amplification between benign breast lesions and breast carcinomas, and whether centrosomal analysis can be of value in the diagnosis and prognosis of breast carcinoma. METHODS: Using immunofluorescence analysis with an antibody against γ-tubulin, we analyzed centrosome abnormalities in fine-needle aspirations of 100 breast lesions (25 cases with benign lesions and 75 cases with carcinomas). RESULTS: We found that centrosome amplifications, including numerical centrosome amplification and structural centrosome amplification, were present in most breast tumors. Cells with numerical centrosome amplification were found in 23 of 25 benign lesions, and in all 75 cases of breast carcinomas. Cells with structural centrosome amplification were found in three of 25 benign lesions, and in 69 of 75 breast carcinomas. The breast carcinomas showed a mean percentage of cells with numerical centrosome amplification of 4.86% and a mean percentage of cells with structural centrosome amplification of 3.98%. These percentages were significantly higher than those in benign lesions, with a numerical centrosome amplification of 2.77% and a structural centrosome amplification of 0.10%. Furthermore, the mean percentage of cells with structural centrosome amplification was significantly associated with HER2/neu overexpression (P < 0.05) and with negative estrogen receptor status (P < 0.05), and had a borderline association with negative progesterone receptor status (P = 0.056) in breast carcinomas. CONCLUSION: Structural centrosome amplification may bear a close relationship with breast carcinoma and may be a potential biomarker for diagnosis and prognosis of breast carcinoma. BioMed Central 2007 2007-07-29 /pmc/articles/PMC2206724/ /pubmed/17662154 http://dx.doi.org/10.1186/bcr1752 Text en Copyright © 2007 Guo 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 Article
Guo, Hui-qin
Gao, Meixia
Ma, Jinfang
Xiao, Ting
Zhao, Lin-lin
Gao, Yanning
Pan, Qin-jing
Analysis of the cellular centrosome in fine-needle aspirations of the breast
title Analysis of the cellular centrosome in fine-needle aspirations of the breast
title_full Analysis of the cellular centrosome in fine-needle aspirations of the breast
title_fullStr Analysis of the cellular centrosome in fine-needle aspirations of the breast
title_full_unstemmed Analysis of the cellular centrosome in fine-needle aspirations of the breast
title_short Analysis of the cellular centrosome in fine-needle aspirations of the breast
title_sort analysis of the cellular centrosome in fine-needle aspirations of the breast
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206724/
https://www.ncbi.nlm.nih.gov/pubmed/17662154
http://dx.doi.org/10.1186/bcr1752
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