Hyperparathyroidism of multiple endocrine neoplasia type 1: candidate gene and parathyroid calcium sensing protein expression

Surgery. 1995 Dec;118(6):924-30; discussion 930-1. doi: 10.1016/s0039-6060(05)80095-9.

Abstract

Background: Hyperparathyroidism affects most patients with multiple endocrine neoplasia type 1 (MEN 1). This study investigates expression of the candidate MEN1 gene phospholipase C beta 3 (PLC beta 3) and expression and function of a putative calcium sensing protein (CAS) in hyperparathyroidism of MEN 1.

Methods: In 31 parathyroid glands from 17 patients with MEN 1, CAS distribution was studied immunohistochemically and parallel sections were explored for PLC beta 3 mRNA expression by in situ hybridization. Enzymatically dispersed parathyroid cells were analyzed for cytoplasmic calcium concentrations [Ca2+]i and parathyroid hormone (PTH) release.

Results: All glands exhibited a heterogeneously reduced CAS immunoreactivity, especially meager in nodularly assembled parathyroid cells. Calcium regulated [Ca2+]i and PTH release tended to be more deranged in the glands possessing the lowest immunostaining. Parathyroid PLC beta 3 invariably was homogeneously expressed, and this included even MEN 1 patients with reduced PLC beta 3 expression in endocrine pancreatic tumors.

Conclusions: The findings support variable calcium insensitivity of [Ca2+]i and PTH release in hyperparathyroidism of MEN 1, apparently coupled to heterogeneously reduced CAS expression. For clarification of the role of PLC beta 3 in MEN 1 parathyroid tumorigenesis further study of this protein is required.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Calcium / metabolism
  • Female
  • Gene Expression*
  • Humans
  • Hyperparathyroidism / complications
  • Hyperparathyroidism / genetics*
  • Immunohistochemistry
  • In Situ Hybridization
  • Male
  • Middle Aged
  • Multiple Endocrine Neoplasia Type 1 / complications
  • Multiple Endocrine Neoplasia Type 1 / genetics*
  • Parathyroid Glands / chemistry
  • Parathyroid Glands / metabolism
  • Parathyroid Hormone / metabolism
  • RNA, Messenger / analysis
  • Receptors, Calcium-Sensing
  • Receptors, Cell Surface / analysis
  • Receptors, Cell Surface / genetics*
  • Type C Phospholipases / analysis
  • Type C Phospholipases / genetics*

Substances

  • Parathyroid Hormone
  • RNA, Messenger
  • Receptors, Calcium-Sensing
  • Receptors, Cell Surface
  • Type C Phospholipases
  • Calcium