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Enhanced tumor formation in mice heterozygous for Blm mutation.
Goss, Kathleen Heppner; Risinger, Mary A; Kordich, Jennifer J; Sanz, Maureen M; Straughen, Joel E; Slovek, Lisa E; Capobianco, Anthony J; German, James; Boivin, Gregory P; Groden, Joanna.
Afiliação
  • Goss KH; Department of Department of Molecular Genetics, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, OH 45267, USA.
Science ; 297(5589): 2051-3, 2002 Sep 20.
Article em En | MEDLINE | ID: mdl-12242442
ABSTRACT
Persons with the autosomal recessive disorder Bloom syndrome are predisposed to cancers of many types due to loss-of-function mutations in the BLM gene, which encodes a recQ-like helicase. Here we show that mice heterozygous for a targeted null mutation of Blm, the murine homolog of BLM, develop lymphoma earlier than wild-type littermates in response to challenge with murine leukemia virus and develop twice the number of intestinal tumors when crossed with mice carrying a mutation in the Apc tumor suppressor. These observations indicate that Blm is a modifier of tumor formation in the mouse and that Blm haploinsufficiency is associated with tumor predisposition, a finding with important implications for cancer risk in humans.
Assuntos
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Base de dados: MEDLINE Assunto principal: Síndrome de Bloom / Linfoma de Células T / Adenosina Trifosfatases / DNA Helicases / Predisposição Genética para Doença / Heterozigoto / Neoplasias Intestinais Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2002 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Síndrome de Bloom / Linfoma de Células T / Adenosina Trifosfatases / DNA Helicases / Predisposição Genética para Doença / Heterozigoto / Neoplasias Intestinais Limite: Animals / Female / Humans / Male Idioma: En Ano de publicação: 2002 Tipo de documento: Article