Coexpression of cyclin D1 and alpha-internexin in oligodendroglial tumors

Brain Tumor Pathol. 2015 Oct;32(4):261-7. doi: 10.1007/s10014-015-0228-2. Epub 2015 Aug 2.

Abstract

Oligodendroglial tumors with neuronal differentiation cases have been reported in recent studies. Oligodendrocyte precursor cells (OPCs) give rise to both oligodendrocytes and neurons; however, little is known about the association between OPCs and oligodendroglial tumors with neuronal differentiation. Previously, we observed the coexpression of cyclin D1, one of the OPC markers, and alpha-internexin (INA) in oligodendroglial tumor cells. INA is a neuronal marker, and has been indicated as an immunohistochemical surrogate of chromosome 1p/19q co-deletion in oligodendroglial tumors. In this study, we investigated the expression status in 83 gliomas immunohistochemically, and found that cyclin D1-positive cells were commonly detected in gliomas. There was no correlation between the cyclin D1 and Ki-67 labeling indices, suggesting an unrecognized role of cyclin D1 other than a cell cycle regulator in gliomas. Cyclin D1/INA double-positive cells were consistently observed in oligodendroglial tumors regardless of histological grade. In 2 cases of oligodendroglioma with neuronal differentiation, the tumor cells of neuronal morphology showed higher expression of INA, suggesting INA expression may be associated with a bona fide neuronal phenotype. The prevalence of cyclin D1/INA double-positive cells is a distinct feature of oligodendroglial tumors. This new characteristic finding may have practical utility in glioma classification.

Keywords: Alpha-internexin; Cyclin D1; Immunohistochemistry; Oligodendrocyte precursor cells; Oligodendroglioma.

MeSH terms

  • Brain Neoplasms / classification
  • Brain Neoplasms / genetics*
  • Brain Neoplasms / pathology
  • Cyclin D1 / genetics*
  • Cyclin D1 / metabolism
  • Cyclin D1 / physiology
  • Gene Expression / genetics*
  • Gene Expression Regulation, Neoplastic / genetics*
  • Humans
  • Immunohistochemistry
  • Intermediate Filament Proteins / genetics*
  • Intermediate Filament Proteins / metabolism
  • Intermediate Filament Proteins / physiology
  • Oligodendroglioma / classification
  • Oligodendroglioma / genetics*
  • Oligodendroglioma / pathology

Substances

  • CCND1 protein, human
  • Intermediate Filament Proteins
  • alpha-internexin
  • Cyclin D1