Pituitary adenoma predisposition caused by germline mutations in the AIP gene.
Outi O Vierimaa,
Marianthi M Georgitsi,
Rainer R Lehtonen,
Pia P Vahteristo,
Antti A Kokko,
Anniina A Raitila,
Karoliina K Tuppurainen,
Tapani M L TM Ebeling,
Pasi I PI Salmela,
Ralf R Paschke,
Sadi S Gündogdu,
Ernesto E De Menis,
Markus J MJ Mäkinen,
Virpi V Launonen,
Auli A Karhu and
Lauri A LA Aaltonen
crossref 312(5777):1228-30 26 May 2006
PMID 16728643
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.
DOI: 10.1126/science.1126100
Version: za2963e q8za3 q8zbd q8zc7 q8zd9 q8ze9 q8zf5 q8zgc
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