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Brain Pathol. 2013 Mar;23(2):200-5. doi: 10.1111/bpa.12021.

Rhabdoid tumors: an initial clue to the role of chromatin remodeling in cancer.

Author information

1
Department of Pediatric Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA.

Abstract

The discovery of biallelic, inactivating SMARCB1 mutations in rhabdoid tumors (RTs) over a decade ago represented the first recognized link between chromatin remodeling and tumor suppression. SMARCB1 is a core subunit of the SWI/SNF chromatin remodeling complex, and the recent emergence of frequent mutations in genes that encode subunits of this complex across a wide variety of cancers suggests that perturbation of this chromatin remodeling complex constitutes a key driver of cancer formation. Despite the highly aggressive nature of RTs, they are genetically simple cancers that appear to lack chromosomal instability and contain very few mutations. Indeed, the mutation rate in RTs is among the lowest of all cancers sequenced, with loss of SMARCB1 as essentially the sole recurrent event. Given the genetic simplicity of this disease, understanding the chromatin dysregulation caused by SMARCB1 loss may provide more general insight into how epigenetic alterations can contribute to oncogenic transformation and may reveal opportunities for targeted therapy not only of RT but also the variety of other SWI/SNF mutant cancers.

PMID:
23432645
DOI:
10.1111/bpa.12021
[Indexed for MEDLINE]

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