Insulin production in a neuroectodermal tumor that expresses islet factor-1, but not pancreatic-duodenal homeobox 1

J Clin Endocrinol Metab. 2001 Apr;86(4):1795-800. doi: 10.1210/jcem.86.4.7429.

Abstract

We studied a 60-yr-old female with a brain tumor who showed severe symptoms of hypoglycemia (plasma glucose, 2.2 mmol/L) and hyperinsulinemia (1.28 nmol/L) after radiotherapy. The cystic brain tumor contained proinsulin and insulin at concentrations of 13.6 and 1.22 nmol/L, respectively. Immunohistochemical studies showed the tumor cells were ectodermal in origin but not endodermal, based on three diagnostic features of neuroectodermal tumors 1) pseudorosette formation noted under light microscopy, 2) finding of a small number of dense core neurosecretory granules on electron microscopy, and 3) positive immunostaining for both neuronal specific enolase and protein gene product 9.5. These cells also expressed the transcription factor, neurogenin-3, NeuroD/beta 2, and islet factor I, which are believed to be transcription factors in neuroectoderm as well as in pancreatic islet cells, but not pancreatic-duodenal homeobox 1, Pax4, or Nkx2.2. In addition, they did not express glucagon, somatostatin, or glucagon-like peptide-1. Our results show the presence of proinsulin in an ectoderm cell brain tumor that does not express the homeobox gene, pancreatic-duodenal homeobox 1, but expresses other transcription factors, i.e. neurogenin3, NeuroD/beta 2, and islet factor-1, which are related to insulin gene expression in the brain tumor.

Publication types

  • Case Reports

MeSH terms

  • Antigens, Differentiation / metabolism
  • Basic Helix-Loop-Helix Transcription Factors
  • Brain / metabolism
  • Brain / pathology
  • Brain Neoplasms / metabolism*
  • Brain Neoplasms / pathology
  • Female
  • Homeodomain Proteins / metabolism*
  • Humans
  • Insulin / biosynthesis*
  • LIM-Homeodomain Proteins
  • Middle Aged
  • Nerve Tissue Proteins / metabolism
  • Neuroectodermal Tumors / metabolism*
  • Neuroectodermal Tumors / pathology
  • Trans-Activators / metabolism*
  • Transcription Factors
  • Ubiquitin Thiolesterase

Substances

  • Antigens, Differentiation
  • Basic Helix-Loop-Helix Transcription Factors
  • Homeodomain Proteins
  • Insulin
  • LIM-Homeodomain Proteins
  • NEUROG3 protein, human
  • Nerve Tissue Proteins
  • Trans-Activators
  • Transcription Factors
  • insulin gene enhancer binding protein Isl-1
  • pancreatic and duodenal homeobox 1 protein
  • Ubiquitin Thiolesterase