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

Masanori Murakami, Takanobu Yoshimoto, Isao Minami, Ryotaro Bouchi, Kyoichiro Tsuchiya, Koshi Hashimoto, Hajime Izumiyama, Yasuhisa Fujii, Takashi Endo, Takumi Akashi, Koshiro Nishimoto, Kuniaki Mukai, Kazunori Kihara, Yoshihiro Ogawa

研究成果: ジャーナルへの寄稿記事

6 引用 (Scopus)

抜粋

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.

元の言語英語
ページ(範囲)328-333
ページ数6
ジャーナルEndocrine Pathology
26
発行部数4
DOI
出版物ステータス出版済み - 12 1 2015
外部発表Yes

    フィンガープリント

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Endocrinology, Diabetes and Metabolism
  • Endocrinology

これを引用

Murakami, M., Yoshimoto, T., Minami, I., Bouchi, R., Tsuchiya, K., Hashimoto, K., ... Ogawa, Y. (2015). A Novel Somatic Deletion Mutation of ATP2B3 in Aldosterone-Producing Adenoma. Endocrine Pathology, 26(4), 328-333. https://doi.org/10.1007/s12022-015-9400-9