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A Novel Somatic Deletion Mutation of ATP2B3 in Aldosterone-Producing Adenoma.

Authors :
Murakami, Masanori
Yoshimoto, Takanobu
Minami, Isao
Bouchi, Ryotaro
Tsuchiya, Kyoichiro
Hashimoto, Koshi
Izumiyama, Hajime
Fujii, Yasuhisa
Endo, Takashi
Akashi, Takumi
Nishimoto, Koshiro
Mukai, Kuniaki
Kihara, Kazunori
Ogawa, Yoshihiro
Source :
Endocrine Pathology; Dec2015, Vol. 26 Issue 4, p328-333, 6p
Publication Year :
2015

Abstract

Aldosterone-producing adenoma (APA) is a form of primary aldosteronism (PA). Recent studies suggested that somatic mutations in the KCNJ5, ATP1A1, ATP2B3, and CACNA1D genes are involved in the pathogenesis of APA. We report a case of a 62-year-old man diagnosed as PA with left adrenal mass. He underwent adrenalectomy for treatment. We identified a novel somatic deletion mutation in ATP2B3 in the adrenal tumor: c.1269_1274delTGTGCT which spans three codons (423-425) resulting in p.Val424_Leu425del. Immunohistochemical analysis revealed strong expression of aldosterone synthase (CYP11B2) in the tumor tissue, which is consistent with APA. Here, we identified a novel somatic deletion mutation in ATP2B3, which results in the amino acid sequences increasing intracellular calcium concentrations as reported previously, leading to increased aldosterone synthase (CYP11B2) expression and following excess aldosterone production in the APA cells. The novel ATP2B3 mutation detected in our case supports the pathogenic significance of the locus spanning the codon 424-426 of ATP2B3. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10463976
Volume :
26
Issue :
4
Database :
Complementary Index
Journal :
Endocrine Pathology
Publication Type :
Academic Journal
Accession number :
111115698
Full Text :
https://doi.org/10.1007/s12022-015-9400-9