Deletions of CDKN2C in multiple myeloma: biological and clinical implications

Leone, P.E. et al. (2008) Deletions of CDKN2C in multiple myeloma: biological and clinical implications. Clinical Cancer Research, 14, pp. 6033-6041. (doi: 10.1158/1078-0432.CCR-08-0347)

Full text not currently available from Enlighten.

Abstract

<p>Purpose: Deletions of chromosome 1 have been described in 7% to 40% of cases of myeloma with inconsistent clinical consequences. CDKN2C at 1p32.3 has been identified in myeloma cell lines as the potential target of the deletion. We tested the clinical impact of 1p deletion and used high-resolution techniques to define the role of CDKN2C in primary patient material.</p> <p>Experimental Design: We analyzed 515 cases of monoclonal gammopathy of undetermined significance (MGUS), smoldering multiple myeloma (SMM), and newly diagnosed multiple myeloma using fluorescence in situ hybridization (FISH) for deletions of CDKN2C. In 78 myeloma cases, we carried out Affymetrix single nucleotide polymorphism mapping and U133 Plus 2.0 expression arrays. In addition, we did mutation, methylation, and Western blotting analysis.</p> <p>Results: By FISH we identified deletion of 1p32.3 (CDKN2C) in 3 of 66 MGUS (4.5%), 4 of 39 SMM (10.3%), and 55 of 369 multiple myeloma cases (15%). We examined the impact of copy number change at CDKN2C on overall survival (OS), and found that the cases with either hemizygous or homozygous deletion of CDKN2C had a worse OS compared with cases that were intact at this region (22 months versus 38 months; P = 0.003). Using gene mapping we identified three homozygous deletions at 1p32.3, containing CDKN2C, all of which lacked expression of CDKN2C. Cases with homozygous deletions of CDKN2C were the most proliferative myelomas, defined by an expression-based proliferation index, consistent with its biological function as a cyclin-dependent kinase inhibitor.</p> <p>Conclusions: Our results suggest that deletions of CDKN2C are important in the progression and clinical outcome of myeloma.</p>

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Dickens, Dr Nicholas
Authors: Leone, P.E., Walker, B.A., Jenner, M.W., Chiecchio, L., Dagrada, G., Protheroe, R.K.M., Johnson, D.C., Dickens, N.J., Brito, J.L., Else, M., Gonzalez, D., Ross, F.M., Chen-Kiang, S., Davies, F.E., and Morgan, G.J.
College/School:College of Medical Veterinary and Life Sciences > School of Infection & Immunity
Journal Name:Clinical Cancer Research
Publisher:American Association for Cancer Research
ISSN:1078-0432
ISSN (Online):1557-3265

University Staff: Request a correction | Enlighten Editors: Update this record