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Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes.
Nikoloski, Gorica; Langemeijer, Saskia M C; Kuiper, Roland P; Knops, Ruth; Massop, Marion; Tönnissen, Evelyn R L T M; van der Heijden, Adrian; Scheele, Theresia N; Vandenberghe, Peter; de Witte, Theo; van der Reijden, Bert A; Jansen, Joop H.
Afiliación
  • Nikoloski G; Department of Laboratory Medicine, Radboud University, Nijmegen Medical Centre, Nijmegen, The Netherlands.
Nat Genet ; 42(8): 665-7, 2010 Aug.
Article en En | MEDLINE | ID: mdl-20601954
ABSTRACT
In myelodysplastic syndromes (MDS), deletions of chromosome 7 or 7q are common and correlate with a poor prognosis. The relevant genes on chromosome 7 are unknown. We report here that EZH2, located at 7q36.1, is frequently targeted in MDS. Analysis of EZH2 deletions, missense and frameshift mutations strongly suggests that EZH2 is a tumor suppressor. As EZH2 functions as a histone methyltransferase, abnormal histone modification may contribute to epigenetic deregulation in MDS.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2010 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Mutación Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Nat Genet Asunto de la revista: GENETICA MEDICA Año: 2010 Tipo del documento: Article País de afiliación: Países Bajos