The IGF-I receptor sub-membrane domain is intact in GH-secreting pituitary tumours

Clin Endocrinol (Oxf). 1995 Feb;42(2):169-72. doi: 10.1111/j.1365-2265.1995.tb01858.x.

Abstract

Background and objective: Clinical acromegaly is characterized by dysregulation of somatotroph GH secretion in the presence of high circulating serum IGF-I levels. Physiologically, IGF-I exerts a negative feedback on GH secretion at both the hypothalamic and the pituitary levels. We have previously shown that the 943 and 950 tyrosine residues in the IGF-I receptor beta-subunit are required for ligand signalling to the GH gene, as substitution of these residues abrogates IGF-I signal transduction. To determine whether a mutation within the IGF-I receptor submembrane domain may be involved in the pathogenesis of GH secreting tumours, we studied this region in these tumours.

Design: Exon 15 of the IGF-I receptor containing both the 943 and 950 tyrosines was analysed in 19 GH-secreting tumours by single-strand conformation polymorphism (SSCP) analysis of polymerase chain reaction (PCR) products. Tumour DNA and patients' lymphocyte DNA, which served as normal controls, were analysed.

Results: All samples exhibited normal migration patterns in the SSCP analysis which was further confirmed by direct DNA sequencing.

Conclusions: We conclude that mutations in the IGF-I receptor sub-membrane domain which disrupt the negative feedback loop are not involved in the pathogenesis of acromegaly.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • DNA, Neoplasm / analysis
  • Exons
  • Growth Hormone / metabolism*
  • Humans
  • Molecular Sequence Data
  • Mutation / genetics
  • Mutation / physiology
  • Pituitary Neoplasms / genetics*
  • Pituitary Neoplasms / metabolism
  • Polymerase Chain Reaction
  • Polymorphism, Single-Stranded Conformational
  • Receptor, IGF Type 1 / genetics*
  • Sequence Analysis, DNA

Substances

  • DNA, Neoplasm
  • Growth Hormone
  • Receptor, IGF Type 1