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Relationship between circulating syndecan-1 levels (CD138s) and serum free light chains in monoclonal gammopathies.

Authors :
Cigliana, Giovanni
Torti, Eleonora
Gulli, Francesca
De Santis, Elena
Dell'Abate, Maria Teresa
Colacicco, Luigi
Pisani, Francesco
Conti, Laura
Basile, Umberto
Source :
Journal of Experimental & Clinical Cancer Research (17569966); Jul2015, Vol. 34 Issue 1, p1-10, 10p
Publication Year :
2015

Abstract

Background: Monoclonal gammopathies encompass a wide range of diseases characterized by the monoclonal expansion of a B-cell clone. Despite emerging therapeutic strategies, chances of survival of patients who are affected are still scarce, which implies that new tools are necessary not only for the diagnosis but also for the follow-up of patients affected by such diseases. In this context, the use of free light chains (FLCs) has been incorporated into many guidelines. Likewise, tumor microenvironment is consistently gaining importance as role player in tumor pathogenesis. Specifically, Syndecan-1 (CD138), a heparan-sulfate proteoglycan is attracting interests as it is highly expressed and shed by myeloma plasma-cells. The aim of our study was to analyze CD138 levels in the serum of patients affected by multiple myeloma or light chain only disease, and to compare the values obtained with free light chain (FLC) kappa, lambda and FLC ratio in both groups of patients. Methods: 84 patients affected by Multiple Myeloma and Light Chain Myeloma were recruited for this study. Serum CD138 was assessed by ELISA (Diaclone Research, France) and FLC values were quantified by nephelometry (Freelite TM Human Kappa and Lambda Free Kits, The Binding Site, UK). Data was analyzed by GraphPad Prism software and Statgraph. Results: We observed higher CD138 mean values in myeloma patients compared to the light chain only myeloma group. A positive linear regression of CD138 and FLC was observed in the light chain only cohort as opposed to myeloma patients which show an inverse trend. Conclusions: The study highlighted an existing relationship between FLCs and CD138 and wishes to seek also a correlation in order to rapidly and efficiently perform diagnosis and different diagnostic schemes. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
17569966
Volume :
34
Issue :
1
Database :
Complementary Index
Journal :
Journal of Experimental & Clinical Cancer Research (17569966)
Publication Type :
Academic Journal
Accession number :
108692244
Full Text :
https://doi.org/10.1186/s13046-015-0155-4