Germline HABP2 Mutation Causing Familial Nonmedullary Thyroid Cancer

N Engl J Med. 2015 Jul 30;373(5):448-55. doi: 10.1056/NEJMoa1502449.

Abstract

Familial nonmedullary thyroid cancer accounts for 3 to 9% of all cases of thyroid cancer, but the susceptibility genes are not known. Here, we report a germline variant of HABP2 in seven affected members of a kindred with familial nonmedullary thyroid cancer and in 4.7% of 423 patients with thyroid cancer. This variant was associated with increased HABP2 protein expression in tumor samples from affected family members, as compared with normal adjacent thyroid tissue and samples from sporadic cancers. Functional studies showed that HABP2 has a tumor-suppressive effect, whereas the G534E variant results in loss of function.

Publication types

  • Case Reports
  • Research Support, N.I.H., Intramural

MeSH terms

  • Adenoma / genetics*
  • Adenoma / metabolism
  • Adenoma / pathology
  • Adolescent
  • Child
  • Female
  • Genetic Predisposition to Disease
  • Germ-Line Mutation*
  • Humans
  • Male
  • Neoplastic Syndromes, Hereditary / genetics*
  • Pedigree
  • Sequence Analysis, DNA
  • Serine Endopeptidases / genetics*
  • Serine Endopeptidases / metabolism
  • Thyroid Neoplasms / genetics*
  • Thyroid Neoplasms / metabolism
  • Thyroid Neoplasms / pathology
  • Young Adult

Substances

  • HABP2 protein, human
  • Serine Endopeptidases