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Prognostic relevance of serum levels and cellular expression of adiponectin in B-cell chronic lymphocytic leukemia.

Authors :
Molica S
Vitelli G
Cutrona G
Todoerti K
Mirabelli R
Digiesi G
Giannarelli D
Sperduti I
Molica M
Gentile M
Morabito F
Neri A
Ferrarini M
Source :
International journal of hematology [Int J Hematol] 2008 Nov; Vol. 88 (4), pp. 374-380. Date of Electronic Publication: 2008 Sep 27.
Publication Year :
2008

Abstract

The correlation between well-established biological parameters of prognostic relevance in B-cell chronic lymphocytic leukaemia (CLL) [i.e., mutational status of the immunoglobulin heavy chain variable region (IgV(H)), ZAP-70- and CD38-expression] and adiponectin serum concentration was evaluated in a cohort of 69 previously untreated Binet stage A CLL patients. Adiponectin levels inversely correlated with absolute peripheral blood lymphocyte count (r = -0.254; P = 0.03), CD38-positive CLL cells (r = -0.294; P = 0.04) and ZAP-70 (r = -0.285; P = 0.03). The univariate Cox proportional hazard model demonstrated that, in addition with lower serum levels of adiponectin (P = 0.01), the unmutated IgV(H) condition (P = 0.002) and ZAP-70-positivity (P = 0.02) were associated with a shorter time to first treatment (TFT). However, in multivariate analysis only ZAP-70 positivity emerged as predictor of the TFT (P = 0.008). The levels of adiponectin in CLL were evaluated in 60 patients from an independent cohort investigated by gene expression profiling. Adiponectin gene expression was invariably low suggesting a limited (if any) role of leukemic cells in the production of circulating adiponectin levels. In contrast, both adiponectin receptor 1 (AdipoR1) and AdipoR2 mRNA were highly expressed by CLL cells with a degree of inter-patient variability. Our results, although preliminary, lend support to the idea that adiponectin secretion by bone marrow adipocytes might represent a possible promising drug target in the field of hematology.

Details

Language :
English
ISSN :
1865-3774
Volume :
88
Issue :
4
Database :
MEDLINE
Journal :
International journal of hematology
Publication Type :
Academic Journal
Accession number :
18818986
Full Text :
https://doi.org/10.1007/s12185-008-0165-5