Pituitary Adenoma Predisposition Caused by Germline Mutations in the AIP Gene

Author:

Vierimaa Outi12345,Georgitsi Marianthi12345,Lehtonen Rainer12345,Vahteristo Pia12345,Kokko Antti12345,Raitila Anniina12345,Tuppurainen Karoliina12345,Ebeling Tapani M. L.12345,Salmela Pasi I.12345,Paschke Ralf12345,Gündogdu Sadi12345,De Menis Ernesto12345,Mäkinen Markus J.12345,Launonen Virpi12345,Karhu Auli12345,Aaltonen Lauri A.12345

Affiliation:

1. Department of Clinical Genetics, Oulu University Hospital, 90029 Oulu, Finland.

2. Department of Internal Medicine, Oulu University Hospital, 90029 Oulu, Finland.

3. Department of Medical Genetics, Molecular and Cancer Biology Research Program, 00014 University of Helsinki, Helsinki, Finland.

4. Department of Pathology, University of Oulu, 90014 Oulu, Finland.

5. Medical Department III, Leipzig University, 04103 Leipzig, Germany.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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