Genomic analysis reveals frequent TRAF7 mutations in intraneural perineuriomas

被引:55
作者
Klein, Christopher J. [1 ,2 ,3 ]
Wu, Yanhong [2 ]
Jentoft, Mark E. [2 ]
Mer, Georges [4 ]
Spinner, Robert J. [5 ]
Dyck, P. James B. [1 ]
Dyck, Peter J. [1 ]
Mauermann, Michelle L. [1 ]
机构
[1] Mayo Clin, Dept Neurol, 200 First St SW, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Lab Med & Pathol, Rochester, MN 55905 USA
[3] Mayo Clin, Dept Med Genet, Rochester, MN 55905 USA
[4] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
[5] Mayo Clin, Dept Neurosurg, Rochester, MN 55905 USA
关键词
SOFT-TISSUE PERINEURIOMA; HYPERTROPHIC NEUROPATHY; CHROMOSOME-22; MENINGIOMAS; KLF4;
D O I
10.1002/ana.24854
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Intraneural perineuriomas are benign peripheral nerve sheath tumors that cause progressive debilitating focal extremity weakness. The etiology of perineuriomas is largely unknown. We utilized whole exome sequencing, copy number algorithm evaluation, and high-resolution whole genome microarray to investigate for a genetic causal link to intraneural perineuriomas. Ten of 16 (60%) tumor cases had mutations in the WD40 domain of TRAF7, the same location for causal mutations of meningiomas. Two additional perineurioma cases had large chromosomal abnormalities in multiple chromosomes, including chromosome 22q. This study identifies a common cause for intraneural perineuriomas and an unexpected shared pathogenesis with intracranial meningiomas. Ann Neurol 2017;81:316-321
引用
收藏
页码:316 / 321
页数:6
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