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Pituitary adenoma predisposition caused by germline mutations in the AIP gene.

Abstract
Pituitary adenomas are common in the general population, and understanding their molecular basis is of great interest. Combining chip-based technologies with genealogy data, we identified germline mutations in the aryl hydrocarbon receptor interacting protein (AIP) gene in individuals with pituitary adenoma predisposition (PAP). AIP acts in cytoplasmic retention of the latent form of the aryl hydrocarbon receptor and also has other functions. In a population-based series from Northern Finland, two AIP mutations account for 16% of all patients diagnosed with pituitary adenomas secreting growth hormone and for 40% of the subset of patients who were diagnosed when they were younger than 35 years of age. Typically, PAP patients do not display a strong family history of pituitary adenoma; thus, AIP is an example of a low-penetrance tumor susceptibility gene.
AuthorsOuti Vierimaa, Marianthi Georgitsi, Rainer Lehtonen, Pia Vahteristo, Antti Kokko, Anniina Raitila, Karoliina Tuppurainen, Tapani M L Ebeling, Pasi I Salmela, Ralf Paschke, Sadi Gündogdu, Ernesto De Menis, Markus J Mäkinen, Virpi Launonen, Auli Karhu, Lauri A Aaltonen
JournalScience (New York, N.Y.) (Science) Vol. 312 Issue 5777 Pg. 1228-30 (May 26 2006) ISSN: 1095-9203 [Electronic] United States
PMID16728643 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Intracellular Signaling Peptides and Proteins
  • Proteins
  • aryl hydrocarbon receptor-interacting protein
Topics
  • Adenoma (genetics)
  • Age of Onset
  • Cohort Studies
  • Female
  • Finland
  • Gene Expression Profiling
  • Genetic Predisposition to Disease
  • Genetic Testing
  • Germ-Line Mutation
  • Growth Hormone-Secreting Pituitary Adenoma (genetics)
  • Haplotypes
  • Heterozygote
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Lod Score
  • Loss of Heterozygosity
  • Male
  • Oligonucleotide Array Sequence Analysis
  • Pedigree
  • Penetrance
  • Pituitary Neoplasms (genetics)
  • Polymorphism, Single Nucleotide
  • Prolactinoma (genetics)
  • Proteins (genetics, physiology)
  • Sex Distribution

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