High-resolution genomic screening in mantle cell lymphoma-specific changes correlate with genomic complexity, the proliferation signature and survival

• Published in: Genes chromosomes & cancer 2011-02, Vol.50 (2), p.113-121
• Main Authors: Halldórsdóttir, Anna M., Sander, Birgitta, Göransson, Hanna, Isaksson, Anders, Kimby, Eva, Mansouri, Mahmoud, Rosenquist, Richard, Ehrencrona, Hans
• Format: Article
• Language: English
• Subjects: Adult; Aged; Aged, 80 and over; Biomarkers, Tumor - genetics; Cell survival; Chromosome Deletion; Cluster Analysis; copy number; DNA Copy Number Variations - genetics; Female; Gene Expression Profiling; Gene Expression Regulation, Neoplastic; Genetic Testing; Genomic analysis; Humans; Kaplan-Meier Estimate; Loss of Heterozygosity; Lymphoma, Mantle-Cell - genetics; Male; mantle cell lymphoma; MEDICIN; Medicin och hälsovetenskap; MEDICINE; Middle Aged; Prognosis; Sequence Deletion; Single-nucleotide polymorphism; Survival; Tumor suppressor genes
• ISSN: 1045-2257; 1098-2264; 1098-2264
• DOI: 10.1002/gcc.20836

Mantle cell lymphoma (MCL) is characterized by the t(11;14)(q13;q32) and numerous copy number aberrations (CNAs). Recently, gene expression profiling defined a proliferation gene expression signature in MCL where high scores predict shorter survival. We investigated 31 MCL cases using high‐density single nucleotide polymorphism arrays and correlated CNA patterns with the proliferation signature and with clinical data. Many recurrent CNAs typical of MCL were detected, including losses at 1p (55%), 8p (29%), 9q (29%), 11q (55%), 13q (42%) and 17p (32%), and gains at 3q (39%), 8q (26%), 15q (23%) and 18q (23%). A novel deleted region at 20q (16%) contained only one candidate gene, ZFP64, a putative tumor suppressor. Unsupervised clustering identified subgroups with different patterns of CNAs, including a subset (19%) characterized by the presence of 11q loss in all cases and by the absence of 13q loss, and 3q and 7p gains. Losses at 1p, 8p, 13q and 17p were associated with increased genomic complexity. High proliferation signature scores correlated with increased number of large (>15 Mbp) CNAs (P = 0.03) as well as copy number gains at 7p (P = 0.02) and losses at 9q (P = 0.04). Furthermore, large/complex 13q losses were associated with improved survival (P < 0.05) as were losses/copy number neutral LOH at 19p13 (P = 0.01). In summary, this high‐resolution genomic analysis identified novel aberrations and revealed that several CNAs correlated with genomic complexity, the proliferation status and survival. © 2010 Wiley‐Liss,Inc.