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Serum YB-1 (Y-box binding protein 1) as a biomarker of bone disease progression in patients with breast cancer and bone metastases

Authors :
A.R. Ferreira
M. Bettencourt
I. Alho
A.L. Costa
A.R. Sousa
A. Mansinho
C. Abreu
C. Pulido
D. Macedo
I. Vendrell
T.R. Pacheco
L. Costa
S. Casimiro
Source :
Journal of Bone Oncology, Vol 6, Iss C, Pp 16-21 (2017)
Publication Year :
2017
Publisher :
Elsevier, 2017.

Abstract

YB-1 (Y-box binding protein 1) is a multifunctional cold-shock protein that has been implicated in all hallmarks of cancer. Elevated YB-1 protein level was associated with poor prognosis in several types of cancers, including breast cancer (BC), where it is a marker of decreased overall survival (OS) and distant metastasis-free survival across all subtypes. YB-1 is also secreted by different cell types and may act as an extracellular mitogen; however the pathological implications of the secreted form of YB-1 (sYB-1) are unknown. Our purpose was to retrospectively evaluate the association between YB-1 measured by ELISA in serum and disease characteristics and outcomes in patients with BC and bone metastases (BM). In our cohort, sYB-1 was detected in the serum of 22 (50%) patients, and was associated with the presence of extra-bone metastases (p=0.044). Positive sYB-1 was also associated with faster bone disease progression (HR 3.1, 95% CI 1.09–8.95, P=0.033), but no significant differences were observed concerning OS, and time to development of skeletal-related events. Moreover, patients with positive sYB-1 also had higher levels of IL-6, a known osteoclastogenic inducer. Therefore, detection of sYB-1 in patients with BC and BM may indicate a higher tumor burden, in bone and extra-bone locations, and is a biomarker of faster bone disease progression.

Details

Language :
English
ISSN :
22121374
Volume :
6
Issue :
C
Database :
Directory of Open Access Journals
Journal :
Journal of Bone Oncology
Publication Type :
Academic Journal
Accession number :
edsdoj.fadbc56e8dfd4726be2f116d72d9a3d2
Document Type :
article
Full Text :
https://doi.org/10.1016/j.jbo.2017.01.002