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Risk of acute promyelocytic leukemia in multiple sclerosis: coding variants of DNA repair genes

  • S. K. Hasan
  • , F. Buttari
  • , T. Ottone
  • , Maria Teresa Voso
  • , Stefan Hohaus
  • , E. Marasco
  • , V. Mantovani
  • , P. Garagnani
  • , M. A. Sanz
  • , L. Cicconi
  • , G. Bernardi
  • , D. Centonze
  • , F. Lo-Coco
  • Clinica Neurologica
  • University of Rome Tor Vergata
  • Alma Mater Studiorum University of Bologna
  • Hospital Universitario La Fe

Risultato della ricerca: Contributo in rivistaArticolopeer review

Abstract

Single nucleotide polymorphisms (SNPs) in double-strand break repair genes may alter DNA repair capacity and, in turn, confer predisposition to leukemia. We analyzed polymorphic variants of DNA repair and detoxification genes in patients with multiple sclerosis (MS) who developed secondary acute promyelocytic leukemia (sAPL), in most cases after treatment with mitoxantrone (MTZ).
Lingua originaleInglese
pagine (da-a)1059-1065
Numero di pagine7
RivistaNeurology
Volume76
DOI
Stato di pubblicazionePubblicato - 2011

Keywords

  • Antineoplastic Agents
  • DNA Repair Enzymes
  • Genetic Predisposition to Disease
  • Humans
  • Leukemia, Promyelocytic, Acute
  • Mitoxantrone
  • Multiple Sclerosis
  • Polymorphism, Single Nucleotide
  • Risk Factors

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