IngentaConnect Splenic marginal zone lymphomas are characterized by loss of inte...

Authors: Vega, Francisco¹; Cho-Vega, Jeong Hee²; Lennon, Patrick A.³; Luthra, Madan G.²; Bailey, Jaime¹; Breeden, Megan¹; Jones, Dan¹; Medeiros, L. Jeffrey¹; Luthra, Rajyalakshmi¹

Source: British Journal of Haematology, Volume 142, Number 2, July 2008 , pp. 216-226(11)

Publisher: Blackwell Publishing

Abstract:

Summary

To further characterize the genotypic features of splenic (S) and nodal (N) marginal zone lymphomas (MZL) we compared eight SMZL and five NMZL by array-based comparative genomic hybridization (aCGH). Arbitrarily, aberrations were divided into major imbalances, defined as gains or losses involving five or more contiguous genetic loci, and minor imbalances, defined as those involving four or fewer loci. SMZL, but not NMZL, demonstrated major imbalances. These included deletions involving various lengths of 7q (three cases), and 14q23q24 (one case) and gains of 9p13p21 (one case), 13q21q33 (one case) and 16p13.1 (one case). Common minor imbalances in SMZL were: loss of sonic hedgehog gene (SHH) at 7q36.2 (four cases), loss of protection of telomere 1 gene (POT1) at 7q31.32 (three cases), and gain of glioma associated oncogene 1 (GLI1) at 12q13.2 (three cases). Common minor alterations in NMZL were: loss of the fas-associated via death domain gene (FADD) at 11q13.2 (three cases) and gain of GLI1 (five cases). In conclusion, SMZL, but not NMZL, demonstrates large genomic imbalances and frequent loss of the 7q31.32 and 7q36.2 regions involving POT1 and SHH, respectively. In NMZL, loss of FADD and gain of GLI1 are frequent events.

Keywords: aCGH; splenic marginal zone lymphoma; nodal marginal zone lymphoma; SHH/GLI1 pathway; POT1 gene

Document Type: Research article

DOI: 10.1111/j.1365-2141.2008.07176.x

Affiliations: 1: Department of Hematopathology 2: Department of Pathology 3: School of Health Sciences, The University of Texas M.D. Anderson Cancer Center, Houston, Texas, USA

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Splenic marginal zone lymphomas are characterized by loss of interstitial regions of chromosome 7q, 7q31.32 and 7q36.2 that include the protection of telomere 1 (POT1) and sonic hedgehog (SHH) genes