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Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.

Creatinine kinase BB (CK-BB) is elevated in many tumours including those of the breast. We have recently described a new, highly sensitive and specific method for measuring CK-BB, based on monoclonal antibodies and time-resolved fluorometry. Using this method, we quantitated CK-BB in 172 breast tumo...

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Autores principales: Zarghami, N., Giai, M., Yu, H., Roagna, R., Ponzone, R., Katsaros, D., Sismondi, P., Diamandis, E. P.
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1996
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074443/
https://www.ncbi.nlm.nih.gov/pubmed/8562347
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author Zarghami, N.
Giai, M.
Yu, H.
Roagna, R.
Ponzone, R.
Katsaros, D.
Sismondi, P.
Diamandis, E. P.
author_facet Zarghami, N.
Giai, M.
Yu, H.
Roagna, R.
Ponzone, R.
Katsaros, D.
Sismondi, P.
Diamandis, E. P.
author_sort Zarghami, N.
collection PubMed
description Creatinine kinase BB (CK-BB) is elevated in many tumours including those of the breast. We have recently described a new, highly sensitive and specific method for measuring CK-BB, based on monoclonal antibodies and time-resolved fluorometry. Using this method, we quantitated CK-BB in 172 breast tumour cytosols and examined the associations between CK-BB and other clinicopathological variables and patient survival. High CK-BB levels were seen more frequently in tumours from patients who were younger (age < 50 years), patients who qualified for chemotherapy and patients with oestrogen receptor-positive tumours. No association was seen between CK-BB and tumour stage, grade, size, histological type or the progesterone receptor. In univariate analysis, the risk of relapse or death was higher in the group with tumours containing high CK-BB levels but the difference did not reach statistical significance. In multivariate analysis, the risk of death was statistically significantly higher in the high-CK-BB group. Analysis of subsets of patients revealed that patients with oestrogen receptor-negative cancer have higher risk of death if their tumours contain high levels of CK-BB. Our data suggest that, in general, CK-BB is associated with more aggressive tumours but its value as a prognostic indicator is limited. CK-BB content of breast tumours may be more useful as an aid in selecting therapy directed at inhibiting this enzyme activity and thus depriving tumour cells of their energy source.
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spelling pubmed-20744432009-09-10 Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients. Zarghami, N. Giai, M. Yu, H. Roagna, R. Ponzone, R. Katsaros, D. Sismondi, P. Diamandis, E. P. Br J Cancer Research Article Creatinine kinase BB (CK-BB) is elevated in many tumours including those of the breast. We have recently described a new, highly sensitive and specific method for measuring CK-BB, based on monoclonal antibodies and time-resolved fluorometry. Using this method, we quantitated CK-BB in 172 breast tumour cytosols and examined the associations between CK-BB and other clinicopathological variables and patient survival. High CK-BB levels were seen more frequently in tumours from patients who were younger (age < 50 years), patients who qualified for chemotherapy and patients with oestrogen receptor-positive tumours. No association was seen between CK-BB and tumour stage, grade, size, histological type or the progesterone receptor. In univariate analysis, the risk of relapse or death was higher in the group with tumours containing high CK-BB levels but the difference did not reach statistical significance. In multivariate analysis, the risk of death was statistically significantly higher in the high-CK-BB group. Analysis of subsets of patients revealed that patients with oestrogen receptor-negative cancer have higher risk of death if their tumours contain high levels of CK-BB. Our data suggest that, in general, CK-BB is associated with more aggressive tumours but its value as a prognostic indicator is limited. CK-BB content of breast tumours may be more useful as an aid in selecting therapy directed at inhibiting this enzyme activity and thus depriving tumour cells of their energy source. Nature Publishing Group 1996-02 /pmc/articles/PMC2074443/ /pubmed/8562347 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Research Article
Zarghami, N.
Giai, M.
Yu, H.
Roagna, R.
Ponzone, R.
Katsaros, D.
Sismondi, P.
Diamandis, E. P.
Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.
title Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.
title_full Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.
title_fullStr Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.
title_full_unstemmed Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.
title_short Creatine kinase BB isoenzyme levels in tumour cytosols and survival of breast cancer patients.
title_sort creatine kinase bb isoenzyme levels in tumour cytosols and survival of breast cancer patients.
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074443/
https://www.ncbi.nlm.nih.gov/pubmed/8562347
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