TERT promoter mutations in periocular carcinomas: implications of ultraviolet light in pathogenesis

Br J Ophthalmol. 2016 Feb;100(2):274-7. doi: 10.1136/bjophthalmol-2015-307503. Epub 2015 Oct 15.

Abstract

Background/aims: Ultraviolet light-signature mutations in the telomerase reverse transcriptase (TERT) gene promoter have been identified in cutaneous melanomas, basal cell carcinomas (BCCs), and squamous cell carcinomas (SCCs). Whether these mutations also occur in periocular tumours, including periocular sebaceous carcinomas (PSCs) and in situ tumours, has not been studied.

Methods: DNA extraction, PCR and Sanger sequencing were used to determine the frequency of TERT promoter mutations in periocular tumours. The presence of mutations was correlated with histological evidence of solar elastosis.

Results: Sixty-three tumours were analysed. TERT promoter mutations were identified in 18 of 22 BCCs (82%), 6 of 10 SCCs (60%), 1 of 2 in situ SCCs (50%), 4 of 9 grade III conjunctival intraepithelial neoplasia (CIN III) (44%) and 0 of 20 PSCs (0%). For BCCs, TERT promoter mutations were not associated with the histological risk categories of the tumours. For CIN III cases, all of the three lesions with solar elastosis had TERT promoter mutations, whereas the mutation was found in only one of the six CIN III cases without solar elastosis.

Conclusions: We demonstrate that ultraviolet light-signature TERT promoter mutations are very common in periocular BCCs, SCCs and CIN III lesions, indicating important roles of ultraviolet light in the pathogenesis of these tumours. In addition, the mutations are present in in situ stage. By contrast, no TERT promoter mutation is found in PSCs.

Keywords: Conjunctiva; Eye Lids; Neoplasia; Pathology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma in Situ / genetics
  • Carcinoma in Situ / pathology
  • Carcinoma, Basal Cell / genetics
  • Carcinoma, Basal Cell / pathology
  • Carcinoma, Squamous Cell / genetics
  • Carcinoma, Squamous Cell / pathology
  • Conjunctival Neoplasms / genetics
  • Conjunctival Neoplasms / pathology
  • DNA Mutational Analysis
  • DNA, Neoplasm / genetics
  • Eyelid Neoplasms / genetics*
  • Eyelid Neoplasms / pathology
  • Humans
  • Mutation*
  • Polymerase Chain Reaction
  • Promoter Regions, Genetic / genetics*
  • Sebaceous Gland Neoplasms / genetics
  • Sebaceous Gland Neoplasms / pathology
  • Sequence Analysis, DNA
  • Skin Aging / genetics
  • Skin Aging / radiation effects*
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology
  • Telomerase / genetics*
  • Ultraviolet Rays / adverse effects*

Substances

  • DNA, Neoplasm
  • TERT protein, human
  • Telomerase