AAGAB Mutations in 18 Canadian Families With Punctate Palmoplantar Keratoderma and a Possible Link to Cancer

J Cutan Med Surg. 2020 Jan/Feb;24(1):28-32. doi: 10.1177/1203475419878161. Epub 2019 Sep 16.

Abstract

Background: Punctate palmoplantar keratoderma type 1 (PPPK1) presents in late childhood to adulthood with multiple small discrete hyperkeratotic papules on palms and soles. PPPK1 is an autosomal dominant skin disease caused by AAGAB mutations. It has been suggested that PPPK1 may be associated with an increased predisposition to systemic malignancies.

Objectives: To evaluate the presence of AAGAB mutations in Canadian families with PPPK1 and the possible increased predisposition to systemic malignancies.

Methods: Eighteen unrelated Canadian families with PPPK1 were recruited for this study. Genomic DNA was extracted from saliva and PCR amplification was performed for all AAGAB exons and exon/intron junctions. PCR products were sequenced and analyzed for mutations. A family history of malignancy was obtained from the index case and, when possible, from other family members.

Results: We have identified 5 heterozygous AAGAB loss of function mutations in 11 families. The mutation c.370 C>T, p.Arg124* was the most prevalent and was identified in 6 families. A splice site mutation, c.451+3delAAGT, was identified in 2 families. The other mutations c.473delG, p.Gly158Glufs*0; c.550-551insAAT, p.Gly183*; and c.505-506 dupAA, p.Asn169Lysfs*6 were each identified in 1 family. Different cancers were reported in 11 families (Table 1 and Supplemental Figure S1).

Conclusions: AAGAB mutations were found in 11 of 18 families with PPPK1. In some families there appears to be an association with cancer.

Keywords: AAGAB mutations; cancer; dermatology; genetics; genotyping; mutation; punctate palmoplantar keratoderma; rare disease.

Publication types

  • Multicenter Study

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics*
  • Adaptor Proteins, Vesicular Transport / metabolism
  • Adult
  • Canada / epidemiology
  • DNA / genetics*
  • DNA Mutational Analysis
  • Female
  • Humans
  • Incidence
  • Keratoderma, Palmoplantar / complications
  • Keratoderma, Palmoplantar / genetics*
  • Keratoderma, Palmoplantar / metabolism
  • Male
  • Middle Aged
  • Mutation*
  • Neoplasms / etiology*
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Pedigree
  • Young Adult

Substances

  • AAGAB protein, human
  • Adaptor Proteins, Vesicular Transport
  • DNA

Supplementary concepts

  • Keratosis palmoplantaris papulosa