The History of the Insulin-Like Growth Factor System

Bradley S. Miller, Alan D. Rogol, Ron G. Rosenfeld

Research output: Contribution to journalReview articlepeer-review

33 Scopus citations

Abstract

The growth hormone (GH)-insulin-like growth factor (IGF) cascade is central to the regulation of growth and metabolism. This article focuses on the history of the components of the IGF system, with an emphasis on the peptide hormones, IGF-I and -II, their cell surface receptors, and the IGF binding proteins (IGFBPs) and IGFBP proteases that regulate the availability of the peptide hormones for interaction with their receptors in relevant target tissues. We describe landmark events in the evolution of the somatomedin hypothesis, including evidence that has become available from experiments at the molecular and cellular levels, whole animal and tissue-specific gene knockouts, studies of cancer epidemiology, identification of prismatic human cases, and short- and long-term clinical trials of IGF-I therapy in humans. In addition, this new evidence has expanded our clinical definition of GH insensitivity (GHI) beyond growth hormone receptor mutations (classic Laron syndrome) to include conditions that cause primary IGF deficiency by impacting post-receptor signal transduction, IGF production, IGF availability to interact with the IGF-I receptor (IGF-1R), and defects in the IGF-1R, itself. We also discuss the clinical aspects of IGFs, from their description as insulin-like activity, to the use of IGF-I in the diagnosis and treatment of GH deficiency, and to the use of recombinant human IGF-I for therapy of children with GHI.

Original languageEnglish (US)
Pages (from-to)619-630
Number of pages12
JournalHormone Research in Paediatrics
Volume95
Issue number6
DOIs
StatePublished - Nov 1 2022

Bibliographical note

Publisher Copyright:
© 2022 S. Karger AG, Basel. Copyright: All rights reserved.

Keywords

  • Acid labile subunit
  • Growth hormone insensitivity
  • hIGF-1 therapy
  • IGF binding protein
  • IGF deficiency
  • Insulin-like growth factor
  • Insulin-like growth factor receptor 1
  • Pregnancy associated plasma protein A/A2

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