Pluripotent tumor cells in benign pituitary adenomas associated with multiple endocrine neoplasia type 1

Cancer Res. 1998 Oct 15;58(20):4715-20.

Abstract

Analysis of human tumor cells in vitro enhances the study of numerous neoplastic conditions. However, it has been difficult to establish long-term cultures of adenoma cells, especially those of neuroendocrine origin, because the endocrine cells survive only briefly in culture, and fibroblasts overgrow the culture dish in 1 or 2 weeks. We describe cells isolated from pituitary adenomas in two patients with multiple endocrine neoplasia type 1 in which cells with a mesenchymal phenotype evolved from pituitary tumor cells. It appears that these poorly differentiated cells arose from multipotent adenoma cells. This represents a path of cell differentiation not observed previously in humans and may help explain the diverse nature of the benign tumors in multiple endocrine neoplasia type 1.

MeSH terms

  • Adenoma / genetics
  • Adenoma / pathology*
  • Cell Differentiation
  • Human Growth Hormone / metabolism
  • Humans
  • In Situ Hybridization, Fluorescence
  • Multiple Endocrine Neoplasia Type 1 / genetics
  • Multiple Endocrine Neoplasia Type 1 / pathology*
  • Neoplasm Proteins / genetics
  • Pituitary Neoplasms / genetics
  • Pituitary Neoplasms / pathology*
  • Proto-Oncogene Proteins*
  • Tumor Cells, Cultured

Substances

  • MEN1 protein, human
  • Neoplasm Proteins
  • Proto-Oncogene Proteins
  • Human Growth Hormone