Expression of c-ErbB2 in human neuroblastoma tissues, adrenal medulla adjacent to tumor, and developing mouse neural crest cells

Am J Pathol. 1995 Mar;146(3):660-72.

Abstract

We have examined the expression of c-ErbB2 in primary neuroblastoma tissues, mouse neural crest-derived tissues, and human adrenal gland adjacent to neuroblastoma tissue and of age-matched controls. c-ErbB2 expression was observed in approximately 60% of cases analyzed, and there were two staining patterns; one showed focal and cytoplasmic and the other showed diffuse and membrane staining patterns. The expression of c-ErbB2 in neuroblastoma tissues was confirmed by reverse transcription polymerase chain reaction and Western blot analysis. Diffuse and membrane staining of c-ErbB2 was well correlated with high urinary catecholamine secretion. In mouse tissues, cytoplasmic expression of c-ErbB2 was observed in immature peripheral neurons and adrenomedullary cells. In mature neurons, the immunoreactivity was confined to the plasma membrane. These results suggest that the expression of c-ErbB2 in neuroblastoma reflects the phenotype of developing peripheral neurons. Postnatal human and mouse adrenomedullary cells lacked c-ErbB2 immunoreactivity, although apparently normal adrenomedullary cells adjacent to neuroblastoma tissues showed strong cytoplasmic expression of c-ErbB2. It is not known whether the phenotypic conversion of adjacent adrenal medullary cells had occurred before or after tumor progression at present.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adrenal Medulla / pathology
  • Adrenal Medulla / physiopathology*
  • Animals
  • Base Sequence
  • Child
  • Child, Preschool
  • Embryo, Mammalian / cytology
  • Embryo, Mammalian / physiology
  • Embryonic and Fetal Development
  • Gene Expression*
  • Genes, erbB-2*
  • Humans
  • Immunohistochemistry
  • Infant
  • Infant, Newborn
  • Male
  • Mice
  • Molecular Probes / genetics
  • Molecular Sequence Data
  • Neural Crest / cytology
  • Neural Crest / physiology*
  • Neuroblastoma / genetics*
  • Neuroblastoma / pathology

Substances

  • Molecular Probes