Molecular Analysis of 11q13 Breakpoints in Multiple Myeloma

Author:

Ronchetti Domenica1,Finelli Palma1,Richelda Raffaella1,Baldini Luca1,Rocchi Mariano1,Viggiano Luigi1,Cuneo Antonio1,Bogni Silvia1,Fabris Sonia1,Lombardi Luigia1,Maiolo Anna Teresa1,Neri Antonino1

Affiliation:

1. From the Laboratorio di Ematologia Sperimentale e Genetica Molecolare, Servizio di Ematologia, Università degli Studi di Milano, Ospedale Maggiore IRCCS, Milano; Istituto di Genetica, Università di Bari, Bari; and Dipartimento di Scienze Biomediche e Terapie Avanzate, Università di Ferrara, Ferrara, Italy.

Abstract

Abstract The t(11;14)(q13;q32) chromosomal translocation, which is the hallmark of mantle cell lymphoma (MCL), is found in approximately 30% of multiple myeloma (MM) tumors with a 14q32 translocation. Although the overexpression of cyclin D1 has been found to be correlated with MM cell lines carrying the t(11;14), rearrangements of theBCL-1/cyclin D1 regions frequently involved in MCL rarely occur in MM cell lines or primary tumors. To test whether specific 11q13 breakpoint clusters may occur in MM, we investigated a representative panel of primary tumors by means of Southern blot analysis using probes derived from MM-associated 11q13 breakpoints. To this end, we first cloned the breakpoints and respective germ-line regions from a primary tumor and the U266 cell line, as well as the germ-line region from the KMS-12 cell line. DNA from 50 primary tumors was tested using a large panel of probes, but a rearrangement was detected in only one case using the KMS-12 breakpoint probe. Our results confirm previous findings that the 11q13 breakpoints in MM are scattered throughout the 11q13 region encompassing the cyclinD1 gene, thus suggesting the absence of 11q13 breakpoint clusters in MM.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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