From Nf1 to Sdhb knockout: Successes and failures in the quest for animal models of pheochromocytoma

Mol Cell Endocrinol. 2016 Feb 5:421:40-8. doi: 10.1016/j.mce.2015.06.027. Epub 2015 Jun 27.

Abstract

Pheochromocytomas and paragangliomas (PPGL) are rare neuroendocrine tumors characterized by a high frequency of hereditary forms. Based on transcriptome classification, PPGL can be classified in two different clusters. Cluster 1 tumors are caused by mutations in SDHx, VHL and FH genes and are characterized by a pseudohypoxic signature. Cluster 2 PPGL carry mutations in RET, NF1, MAX or TMEM127 genes and display an activation of the MAPK and mTOR signaling pathways. Many genetically engineered and allografted mouse models have been generated these past 30 years to investigate the mechanisms of PPGL tumorigenesis and test new therapeutic strategies. Among them, only Cluster 2-related models have been successful while no Cluster 1-related knockout mouse was so far reported to develop a PPGL. In this review, we present an overview of existing, successful or not, PPGL models, and a description of our own experience on the quest of Sdhb knockout mouse models of PPGL.

Keywords: Chromaffin cells; Genetically engineered mouse; Knockout; Pheochromocytoma; Xenograft.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adrenal Gland Neoplasms / genetics*
  • Adrenal Gland Neoplasms / pathology
  • Animals
  • Humans
  • MAP Kinase Signaling System
  • Mice
  • Mice, Knockout
  • Mutation
  • Neurofibromin 1 / genetics*
  • Pheochromocytoma / genetics*
  • Pheochromocytoma / pathology
  • Succinate Dehydrogenase / genetics*

Substances

  • Neurofibromin 1
  • SDHB protein, human
  • Succinate Dehydrogenase