Akting and cycling: a tale of the pituitary

Horm Res. 2004:62 Suppl 3:117-23. doi: 10.1159/000080512.

Abstract

Pituitary tumours are characterized by a series of phenotypic abnormalities, but the molecular nature of the underlying defects has proved peculiarly intractable. Oncogenes and tumour suppressor genes involved in other tumours do not appear to play a major role in the pathogenesis of pituitary tumours. In addition, germline genetic disorders in which pituitary tumours are a common feature have not shed much light on the more common sporadic tumour. A number of defects in specific feedback regulation in the secretory tumours have been identified, but it is presently unclear as to what extent these are a consequence of the tumour, possibly enhancing its growth or survival, rather than the cause. However, recent studies on the cell cycle have demonstrated significant abnormalities that have been traced to a cytoplasmic kinase which appears to be abnormally expressed in the majority of pituitary adenomas, and we are beginning to see a possible unifying abnormality.

Publication types

  • Review

MeSH terms

  • Adenoma / metabolism
  • Animals
  • Cell Cycle*
  • Feedback, Physiological
  • Humans
  • Pituitary Gland / cytology*
  • Pituitary Gland / metabolism*
  • Pituitary Neoplasms / etiology*
  • Pituitary Neoplasms / metabolism
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt

Substances

  • Proto-Oncogene Proteins
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt