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Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?

BACKGROUND: Breast and prostate cancer patients often develop lesions of locally high bone turnover, when the primary tumor metastasizes to the bone causing an abnormal high bone resorption at this site. The objective of the present study was to determine whether local increased bone turnover in bre...

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Autores principales: Leeming, Diana J, Byrjalsen, Inger, Qvist, Per, Koizumi, Mitsuru, Lynnerup, Niels, Fregerslev, Michael, Sørensen, Mette G, Christiansen, Claus, Karsdal, Morten A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453141/
https://www.ncbi.nlm.nih.gov/pubmed/18588674
http://dx.doi.org/10.1186/1471-2407-8-180
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author Leeming, Diana J
Byrjalsen, Inger
Qvist, Per
Koizumi, Mitsuru
Lynnerup, Niels
Fregerslev, Michael
Sørensen, Mette G
Christiansen, Claus
Karsdal, Morten A
author_facet Leeming, Diana J
Byrjalsen, Inger
Qvist, Per
Koizumi, Mitsuru
Lynnerup, Niels
Fregerslev, Michael
Sørensen, Mette G
Christiansen, Claus
Karsdal, Morten A
author_sort Leeming, Diana J
collection PubMed
description BACKGROUND: Breast and prostate cancer patients often develop lesions of locally high bone turnover, when the primary tumor metastasizes to the bone causing an abnormal high bone resorption at this site. The objective of the present study was to determine whether local increased bone turnover in breast and prostate cancer patients is associated with an increase in cartilage degradation and to test in vitro whether osteoclasts or cathepsin K alone generate CTXII from human bone. METHODS: The study included 132 breast and prostate cancer patient, where presence of bone metastases was graded according to the Soloway score. Total bone resorption (CTXI(total)) and cartilage degradation (CTXII) were determined. RESULTS: Breast and prostate cancer patients with bone metastases revealed significant increased levels of CTXI(total )at Soloway scores 1 and higher compared to patients without bone metastases (p < 0.001). CTXII was statistically elevated at score 3 and 4 (p < 0.01). CTXII/CTXI(total )significantly decreased at score 3 and 4 (p < 0.001). Levels of CTXI(total), CTXII and CTXII/CTXI(total )changed +900%, +130%, and -90%, respectively at Soloway score 4 compared to score 0. The in vitro experiments revealed that osteoclasts released CTXI fragments but not CTXII from bone specimens. The same was observed for cathepsin K. CONCLUSION: Data suggest that an uncoupling between bone resorption and cartilage degradation occurs in breast and lung cancer patient.
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spelling pubmed-24531412008-07-11 Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation? Leeming, Diana J Byrjalsen, Inger Qvist, Per Koizumi, Mitsuru Lynnerup, Niels Fregerslev, Michael Sørensen, Mette G Christiansen, Claus Karsdal, Morten A BMC Cancer Research Article BACKGROUND: Breast and prostate cancer patients often develop lesions of locally high bone turnover, when the primary tumor metastasizes to the bone causing an abnormal high bone resorption at this site. The objective of the present study was to determine whether local increased bone turnover in breast and prostate cancer patients is associated with an increase in cartilage degradation and to test in vitro whether osteoclasts or cathepsin K alone generate CTXII from human bone. METHODS: The study included 132 breast and prostate cancer patient, where presence of bone metastases was graded according to the Soloway score. Total bone resorption (CTXI(total)) and cartilage degradation (CTXII) were determined. RESULTS: Breast and prostate cancer patients with bone metastases revealed significant increased levels of CTXI(total )at Soloway scores 1 and higher compared to patients without bone metastases (p < 0.001). CTXII was statistically elevated at score 3 and 4 (p < 0.01). CTXII/CTXI(total )significantly decreased at score 3 and 4 (p < 0.001). Levels of CTXI(total), CTXII and CTXII/CTXI(total )changed +900%, +130%, and -90%, respectively at Soloway score 4 compared to score 0. The in vitro experiments revealed that osteoclasts released CTXI fragments but not CTXII from bone specimens. The same was observed for cathepsin K. CONCLUSION: Data suggest that an uncoupling between bone resorption and cartilage degradation occurs in breast and lung cancer patient. BioMed Central 2008-06-27 /pmc/articles/PMC2453141/ /pubmed/18588674 http://dx.doi.org/10.1186/1471-2407-8-180 Text en Copyright © 2008 Leeming 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
Leeming, Diana J
Byrjalsen, Inger
Qvist, Per
Koizumi, Mitsuru
Lynnerup, Niels
Fregerslev, Michael
Sørensen, Mette G
Christiansen, Claus
Karsdal, Morten A
Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
title Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
title_full Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
title_fullStr Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
title_full_unstemmed Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
title_short Does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
title_sort does increased local bone resorption secondary to breast and prostate cancer result in increased cartilage degradation?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2453141/
https://www.ncbi.nlm.nih.gov/pubmed/18588674
http://dx.doi.org/10.1186/1471-2407-8-180
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