Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

Cancer Res. 1999 Jan 15;59(2):290-3.

Abstract

Heterozygous germ-line mutations in the DNA mismatch repair genes lead to hereditary nonpolyposis colorectal cancer. The disease susceptibility of individuals who constitutionally lack both wild-type alleles is unknown. We have identified three offspring in a hereditary nonpolyposis colorectal cancer family who developed hematological malignancy at a very early age, and at least two of them displayed signs of neurofibromatosis type 1 (NF1). DNA sequence analysis and allele-specific amplification in two siblings revealed a homozygous MLH1 mutation (C676T-->Arg226Stop). Thus, a homozygous germ-line MLH1 mutation and consequent mismatch repair deficiency results in a mutator phenotype characterized by leukemia and/or lymphoma associated with neurofibromatosis type 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • DNA / chemistry
  • DNA Repair*
  • Female
  • Genetic Predisposition to Disease*
  • Germ-Line Mutation*
  • Hematologic Neoplasms / genetics*
  • Humans
  • Male
  • MutL Protein Homolog 1
  • Neoplasm Proteins / deficiency
  • Neoplasm Proteins / genetics*
  • Neurofibromatosis 1 / genetics*
  • Nuclear Proteins

Substances

  • Adaptor Proteins, Signal Transducing
  • Carrier Proteins
  • MLH1 protein, human
  • Neoplasm Proteins
  • Nuclear Proteins
  • DNA
  • MutL Protein Homolog 1