PHF6 mutations in T-cell acute lymphoblastic leukemia

Nat Genet. 2010 Apr;42(4):338-42. doi: 10.1038/ng.542. Epub 2010 Mar 14.

Abstract

Tumor suppressor genes on the X chromosome may skew the gender distribution of specific types of cancer. T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy with an increased incidence in males. In this study, we report the identification of inactivating mutations and deletions in the X-linked plant homeodomain finger 6 (PHF6) gene in 16% of pediatric and 38% of adult primary T-ALL samples. Notably, PHF6 mutations are almost exclusively found in T-ALL samples from male subjects. Mutational loss of PHF6 is importantly associated with leukemias driven by aberrant expression of the homeobox transcription factor oncogenes TLX1 and TLX3. Overall, these results identify PHF6 as a new X-linked tumor suppressor in T-ALL and point to a strong genetic interaction between PHF6 loss and aberrant expression of TLX transcription factors in the pathogenesis of this disease.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Carrier Proteins / genetics*
  • Child
  • Chromosomes, Human, X*
  • Comparative Genomic Hybridization
  • DNA Copy Number Variations
  • Female
  • Genes, Tumor Suppressor*
  • Genetic Linkage
  • Homeodomain Proteins / genetics*
  • Humans
  • Male
  • Mutation
  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma
  • Proto-Oncogene Proteins / genetics*
  • Repressor Proteins

Substances

  • Carrier Proteins
  • Homeodomain Proteins
  • PHF6 protein, human
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • TLX3 protein, human
  • TLX1 protein, human