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Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors

BACKGROUND: The cell cycle is promoted by activation of cyclin dependent kinases (Cdks), which are regulated positively by cyclins and negatively by Cdk inhibitors. Proliferation of carcinoma is associated with altered regulation of the cell cycle. Little is known on the combined alterations of cycl...

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Autores principales: Boström, Pia, Söderström, Mirva, Palokangas, Tuire, Vahlberg, Tero, Collan, Yrjö, Carpen, Olli, Hirsimäki, Pirkko
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716358/
https://www.ncbi.nlm.nih.gov/pubmed/19615042
http://dx.doi.org/10.1186/1756-0500-2-140
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author Boström, Pia
Söderström, Mirva
Palokangas, Tuire
Vahlberg, Tero
Collan, Yrjö
Carpen, Olli
Hirsimäki, Pirkko
author_facet Boström, Pia
Söderström, Mirva
Palokangas, Tuire
Vahlberg, Tero
Collan, Yrjö
Carpen, Olli
Hirsimäki, Pirkko
author_sort Boström, Pia
collection PubMed
description BACKGROUND: The cell cycle is promoted by activation of cyclin dependent kinases (Cdks), which are regulated positively by cyclins and negatively by Cdk inhibitors. Proliferation of carcinoma is associated with altered regulation of the cell cycle. Little is known on the combined alterations of cyclins A, B1, D1 and E in breast cancer in relation to the tumour grade and other prognostic factors. FINDINGS: Immunohistochemical analysis of cyclins A, B1, D1 and E, estrogen receptor, progesterone receptor, Ki-67, Her-2/neu and CK5/6 was performed on 53 breast carcinomas. mRNA levels of the cyclins were analysed of 12 samples by RT-PCR. The expression of cyclins A, B1 and E correlated with each other, while cyclin D1 correlated with none of these cyclins. Cyclins A, B1 and E showed association with tumour grade, Her-2/neu and Ki-67. Cyclin E had a negative correlation with hormone receptors and a positive correlation with triple negative carcinomas. Cyclin D1 had a positive correlation with ER, PR and non-basal breast carcinomas. CONCLUSION: Cyclin A, B1 and E overexpression correlates to grade, Ki-67 and Her2/neu expression. Overexpression of cyclin D1 has a positive correlation with receptor status and non-basal carcinomas suggesting that cyclin D1 expression might be a marker of good prognosis. Combined analysis of cyclins indicates that cyclin A, B and E expression is similarly regulated, while other factors regulate cyclin D1 expression. The results suggest that the combined immunoreactivity of cyclins A, B1, D and E might be a useful prognostic factor in breast cancer.
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spelling pubmed-27163582009-07-28 Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors Boström, Pia Söderström, Mirva Palokangas, Tuire Vahlberg, Tero Collan, Yrjö Carpen, Olli Hirsimäki, Pirkko BMC Res Notes Short Report BACKGROUND: The cell cycle is promoted by activation of cyclin dependent kinases (Cdks), which are regulated positively by cyclins and negatively by Cdk inhibitors. Proliferation of carcinoma is associated with altered regulation of the cell cycle. Little is known on the combined alterations of cyclins A, B1, D1 and E in breast cancer in relation to the tumour grade and other prognostic factors. FINDINGS: Immunohistochemical analysis of cyclins A, B1, D1 and E, estrogen receptor, progesterone receptor, Ki-67, Her-2/neu and CK5/6 was performed on 53 breast carcinomas. mRNA levels of the cyclins were analysed of 12 samples by RT-PCR. The expression of cyclins A, B1 and E correlated with each other, while cyclin D1 correlated with none of these cyclins. Cyclins A, B1 and E showed association with tumour grade, Her-2/neu and Ki-67. Cyclin E had a negative correlation with hormone receptors and a positive correlation with triple negative carcinomas. Cyclin D1 had a positive correlation with ER, PR and non-basal breast carcinomas. CONCLUSION: Cyclin A, B1 and E overexpression correlates to grade, Ki-67 and Her2/neu expression. Overexpression of cyclin D1 has a positive correlation with receptor status and non-basal carcinomas suggesting that cyclin D1 expression might be a marker of good prognosis. Combined analysis of cyclins indicates that cyclin A, B and E expression is similarly regulated, while other factors regulate cyclin D1 expression. The results suggest that the combined immunoreactivity of cyclins A, B1, D and E might be a useful prognostic factor in breast cancer. BioMed Central 2009-07-17 /pmc/articles/PMC2716358/ /pubmed/19615042 http://dx.doi.org/10.1186/1756-0500-2-140 Text en Copyright © 2009 Hirsimäki 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 Short Report
Boström, Pia
Söderström, Mirva
Palokangas, Tuire
Vahlberg, Tero
Collan, Yrjö
Carpen, Olli
Hirsimäki, Pirkko
Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors
title Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors
title_full Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors
title_fullStr Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors
title_full_unstemmed Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors
title_short Analysis of cyclins A, B1, D1 and E in breast cancer in relation to tumour grade and other prognostic factors
title_sort analysis of cyclins a, b1, d1 and e in breast cancer in relation to tumour grade and other prognostic factors
topic Short Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2716358/
https://www.ncbi.nlm.nih.gov/pubmed/19615042
http://dx.doi.org/10.1186/1756-0500-2-140
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