Germline POLE mutation in a child with hypermutated medulloblastoma and features of constitutional mismatch repair deficiency

Cold Spring Harb Mol Case Stud. 2019 Oct 23;5(5):a004499. doi: 10.1101/mcs.a004499. Print 2019 Oct.

Abstract

Ultra-hypermutation (>100 mutations/Mb) is rare in childhood cancer genomes and has been primarily reported in patients with constitutional mismatch repair deficiency (CMMRD) caused by biallelic germline mismatch repair (MMR) gene mutations. We report a 5-yr-old child with classic clinical features of CMMRD and an ultra-hypermutated medulloblastoma with retained MMR protein expression and absence of germline MMR mutations. Mutational signature analysis of tumor panel sequencing data revealed a canonical DNA polymerase-deficiency-associated signature, prompting further genetic testing that uncovered a germline POLE p.A456P missense variant, which has previously been reported as a recurrent somatic driver mutation in cancers. This represents the earliest known onset of malignancy in a patient with a germline mutation in the POLE proofreading polymerase. The clinical features in this child, virtually indistinguishable from those of CMMRD, suggest that polymerase-proofreading deficiency should be considered in the differential diagnosis of CMMRD patients with retained MMR function.

Keywords: cerebellar medulloblastoma.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Brain Neoplasms / genetics*
  • Brain Neoplasms / metabolism
  • Cerebellar Neoplasms
  • Child, Preschool
  • Colorectal Neoplasms / genetics*
  • Colorectal Neoplasms / metabolism
  • DNA Mismatch Repair / genetics
  • DNA Mutational Analysis
  • DNA Polymerase II / genetics*
  • DNA Polymerase II / metabolism
  • DNA-Binding Proteins / genetics
  • Female
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Germ Cells / metabolism
  • Germ-Line Mutation / genetics
  • Humans
  • Medulloblastoma / genetics*
  • Medulloblastoma / metabolism
  • Mutation
  • Neoplastic Syndromes, Hereditary / genetics*
  • Neoplastic Syndromes, Hereditary / metabolism
  • Phenotype
  • Poly-ADP-Ribose Binding Proteins / genetics*
  • Poly-ADP-Ribose Binding Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • Poly-ADP-Ribose Binding Proteins
  • DNA Polymerase II
  • POLE protein, human

Supplementary concepts

  • Turcot syndrome