Cellular Oncology (Jan 2008)

Hypermethylation of the FANCC and FANCL Promoter Regions in Sporadic Acute Leukaemia

  • C. J. Hess,
  • N. Ameziane,
  • G. J. Schuurhuis,
  • A. Errami,
  • F. Denkers,
  • G. J. L. Kaspers,
  • J. Cloos,
  • H. Joenje,
  • D. Reinhardt,
  • G. J. Ossenkoppele,
  • C. M. Zwaan,
  • Q. Waisfisz

DOI
https://doi.org/10.3233/CLO-2008-0426
Journal volume & issue
Vol. 30, no. 4
pp. 299 – 306

Abstract

Read online

Objective: Inactivation of the FA-BRCA pathway results in chromosomal instability. Fanconi anaemia (FA) patients have an inherited defect in this pathway and are strongly predisposed to the development of acute myeloid leukaemia (AML). Studies in sporadic cancers have shown promoter methylation of the FANCF gene in a significant proportion of various solid tumours. However, only a single leukaemic case with methylation of one of the FA-BRCA genes has been described to date, i.e. methylation of FANCF in cell line CHRF-288. We investigated the presence of aberrant methylation in 11 FA-BRCA genes in sporadic cases of leukaemia.