Literature DB >> 21785431

Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma.

Timothy Best1, Dalin Li, Andrew D Skol, Tomas Kirchhoff, Sarah A Jackson, Yutaka Yasui, Smita Bhatia, Louise C Strong, Susan M Domchek, Katherine L Nathanson, Olufunmilayo I Olopade, R Stephanie Huang, Thomas M Mack, David V Conti, Kenneth Offit, Wendy Cozen, Leslie L Robison, Kenan Onel.   

Abstract

Survivors of pediatric Hodgkin's lymphoma are at risk for radiation therapy-induced second malignant neoplasms (SMNs). We identified two variants at chromosome 6q21 associated with SMNs in survivors of Hodgkin's lymphoma treated with radiation therapy as children but not as adults. The variants comprise a risk locus associated with decreased basal expression of PRDM1 (encoding PR domain containing 1, with ZNF domain) and impaired induction of the PRDM1 protein after radiation exposure. These data suggest a new gene-exposure interaction that may implicate PRDM1 in the etiology of radiation therapy-induced SMNs.

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Year:  2011        PMID: 21785431      PMCID: PMC3229923          DOI: 10.1038/nm.2407

Source DB:  PubMed          Journal:  Nat Med        ISSN: 1078-8956            Impact factor:   53.440


  20 in total

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  66 in total

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9.  Genetically mediated Nf1 loss in mice promotes diverse radiation-induced tumors modeling second malignant neoplasms.

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