| Literature DB >> 28132860 |
Joshua R Menke1, George Vasmatzis2, Stephen Murphy2, Lin Yang2, David M Menke3, Han W Tun4, Rebecca L King5, Stephanie A Smoley5, Rhett P Ketterling5, William R Sukov6.
Abstract
Mantle cell lymphoma (MCL) is typically characterized by t(11;14), which places the IGH@ enhancer elements upstream of CCND1. This fusion results in up-regulation of CCND1 and consequently its protein product cyclin D1. Recent studies have shown that in MCL, mutations or translocations occurring within the 3' untranslated region (UTR) of the CCND1 gene can result in a truncated mRNA transcript that is more stable and associated with more aggressive disease. We identified a case of MCL showing cyclin D1 overexpression by immunohistochemistry and a t(11;12)(q13;p11.2) by conventional cytogenetic studies. Next-generation genomic sequencing indicated a chromosomal break through the CCND1 3'-UTR and fusion with a non-coding region of chromosome 12. We suggest that, in the absence of the typical CCND1/IGH@ fusion, this rearrangement promotes MCL pathogenesis by eliminating miRNA interaction elements within the 3'-UTR of the CCND1 mRNA transcript consequently resulting in CCND1 overexpression.Entities:
Keywords: 3′-UTR; CCND1; Cytogenetics; Mantle cell lymphoma; Mate-pair sequencing; Translocation; microRNA
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Year: 2017 PMID： 28132860 DOI： 10.1016/j.humpath.2017.01.001
Source DB: PubMed Journal: Hum Pathol ISSN： 0046-8177 Impact factor: 3.466