Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development

Jeremie Vitte, Fuying Gao, Giovanni Coppola, Alexander R. Judkins and Marco Giovannini ()
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Jeremie Vitte: University of California Los Angeles
Fuying Gao: University of California Los Angeles
Giovanni Coppola: University of California Los Angeles
Alexander R. Judkins: University of Southern California
Marco Giovannini: University of California Los Angeles

Nature Communications, 2017, vol. 8, issue 1, 1-13

Abstract: Abstract Germline mutations of the SMARCB1 gene predispose to two distinct tumor syndromes: rhabdoid tumor predisposition syndrome, with malignant pediatric tumors mostly developing in brain and kidney, and familial schwannomatosis, with adulthood benign tumors involving cranial and peripheral nerves. The mechanisms by which SMARCB1 germline mutations predispose to rhabdoid tumors versus schwannomas are still unknown. Here, to understand the origin of these two types of SMARCB1-associated tumors, we generated different tissue- and developmental stage-specific conditional knockout mice carrying Smarcb1 and/or Nf2 deletion. Smarcb1 loss in early neural crest was necessary to initiate tumorigenesis in the cranial nerves and meninges with typical histological features and molecular profiles of human rhabdoid tumors. By inducing Smarcb1 loss at later developmental stage in the Schwann cell lineage, in addition to biallelic Nf2 gene inactivation, we generated the first mouse model developing schwannomas with the same underlying gene mutations found in schwannomatosis patients.

Date: 2017
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DOI: 10.1038/s41467-017-00346-5

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