RARE-22. GERMLINE PATHOGENIC VARIANT c.1552G>A;p.E518K IN DGCR8 CONFERS SUSCEPTIBILITY FOR SCHWANNOMATOSIS AND THYROID TUMORS. (4th December 2020)

• Record Type: Journal Article
• Authors: Chong, Anne-Sophie; Nadaf, Javad; Grau, Elia; Apellaniz-Ruiz, Maria; Fahiminiya, Somayyeh; Saskin, Avi; Han, HyeRim; Turcotte, Robert; Muchantef, Karl; Thomas, Christian; Wagener, Rabea; Bassenden, Angelia; Mete, Ozgur; Pusztaszeri, Marc; Paulus, Werner; Berghuis, Albert; Siebert, Reiner; Albrecht, Steffen; Hasselblatt, Martin; Lazaro, Conxi; Teule, Alexander; Fabian, Marc; Brunet, Joan; Foulkes, William; Rivera, Barbara
• Is Part Of: Neuro-oncology. Volume 22(2020)Supplement 3
• Page Start: iii447
• Page End: iii447
• Publication Date: 2020-12-04
• Subjects: Brain Neoplasms -- Periodicals; Brain -- Tumors -- Periodicals; Brain -- Cancer -- Periodicals; Nervous system -- Cancer -- Periodicals; 616.99481
• DOI: 10.1093/neuonc/noaa222.733
• Languages: English
• ISSNs: 1522-8517

Abstract

Abstract: Germline mutations in DICER1 cause a pleiotropic susceptibility syndrome characterized by the development of pediatric or early-onset tumors including pleuropulmonary blastoma, Wilms tumors, pineoblastomas, multinodular goiter (MNG) and thyroid cancers. Somatic mutations in the other two microprocessors DROSHA and DGCR8 have been found in Wilms Tumors and pineoblastomas. We present here two families with peripheral schwannomatosis and thyroid tumors carrying a germline variant c.1552G>A;p.E518K in DGCR8 . Family one had six affected members with early-onset MNG and five of them developed schwannomatosis. All five members were heterozygous for the variant. One of the carriers had also been diagnosed with a choroid plexus papilloma at 7 years old. The common second event in all tumors tested was the loss of chromosome 22 at the somatic level. In family two, a 35-year-old male was diagnosed with a peripheral schwannoma at the age of 12. Since then, he has developed seven extra peripheral schwannomas (one of which was an ancient schwannoma) and papillary thyroid cancer. DGCR8 lies on chromosome 22q, adjacent to the three schwannoma genes: LZTR1, SMARCB1 and NF2. The variant, c.1552G>A;p.E518K localizes to the first RNA-binding domain of DGCR8 and structural modelling predicts that it abolishes proper binding of RNA. It is also a hotspot somatic mutation in Wilms tumors. Using miRNA profiling, we show that this variant disrupts global microRNA production and DGCR8 mutated tumors show a specific miRNA profile different from DGCR8 wild type tumors. These findings reinforce DGCR8 as a novel susceptibility gene for schwannomatosis and thyroid tumors.