Germline and somatic DICER1 mutations in a pituitary blastoma causing infantile-onset Cushing's disease

J Clin Endocrinol Metab. 2014 Aug;99(8):E1487-92. doi: 10.1210/jc.2014-1016. Epub 2014 May 13.

Abstract

Context: Pituitary blastoma causing Cushing's syndrome in infancy is very rare, and its molecular pathomechanism is not well understood.

Objective: Our objective was to identify genetic changes of a pituitary blastoma causing infantile-onset Cushing's syndrome in a Thai girl without a family history of cancers.

Methods: Genomic DNA from both leukocytes and tumor tissues was used for whole-exome sequencing (WES) and Sanger sequencing of DICER1. The cDNA reverse-transcribed from RNA extracted from both leukocytes and tumor tissues was used for Sanger sequencing, quantitative real-time PCR (qRT-PCR), and pyrosequencing of DICER1.

Results: WES of leukocytes identified a novel heterozygous c.3046delA (p.S1016VfsX1065) mutation in the DICER1 gene. WES of the tumor tissues detected the same frameshift germline mutation and another novel somatic missense c.5438A→T (p.E1813V) mutation. Both mutations were validated by Sanger sequencing. Quantitative real-time PCR revealed that the DICER1 mRNA levels of the tumor tissues were 54% compared with those of her leukocytes. Pyrosequencing showed that the deletion allele constituted 12% and 0% of the DICER1 cDNA of the proband's leukocytes and tumor tissues, respectively.

Conclusion: Our study extends the phenotypic and mutational spectrum of DICER1 mutations to include infantile-onset Cushing's disease and 2 novel mutations. Loss of function of both DICER1 alleles appears to be crucial to initiate tumor development.

Publication types

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

MeSH terms

  • Age Factors
  • DEAD-box RNA Helicases / genetics*
  • Female
  • Germ-Line Mutation*
  • Humans
  • Infant
  • Mutation, Missense*
  • Neoplasms, Germ Cell and Embryonal / complications
  • Neoplasms, Germ Cell and Embryonal / genetics*
  • Pituitary ACTH Hypersecretion / genetics*
  • Pituitary Neoplasms / complications
  • Pituitary Neoplasms / genetics*
  • Ribonuclease III / genetics*
  • Thailand

Substances

  • DICER1 protein, human
  • Ribonuclease III
  • DEAD-box RNA Helicases