| Literature DB >> 26481629 |
Masanori Murakami1, Takanobu Yoshimoto2, Isao Minami1, Ryotaro Bouchi1, Kyoichiro Tsuchiya1, Koshi Hashimoto1,3, Hajime Izumiyama1,4, Yasuhisa Fujii5, Takashi Endo6, Takumi Akashi6, Koshiro Nishimoto7,8, Kuniaki Mukai8, Kazunori Kihara5, Yoshihiro Ogawa1.
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.Entities:
Keywords: ATP2B3; Aldosterone-producing adenoma; CYP11B2; Primary aldosteronism
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Year: 2015 PMID: 26481629 DOI: 10.1007/s12022-015-9400-9
Source DB: PubMed Journal: Endocr Pathol ISSN: 1046-3976 Impact factor: 3.943