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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/13615


    Title: Characterization of a mutated KCNJ5 gene, G387R, in unilateral primary aldosteronism
    Authors: Chueh, JS;Peng, KY;Wu, VC;Shuo-Meng, W;Chieh-Kai, C;Chen, YM;Ke, YY;Pan, CY;Liao, HW
    Contributors: Institute of Biotechnology and Pharmaceutical Research
    Abstract: Somatic mutation in the KCNJ5 gene is a common driver of autonomous aldosterone overproduction in aldosterone-producing adenomas (APA). KCNJ5 mutations contribute to a loss of potassium selectivity and an inward Na+ current could be detected in cells transfected with mutated KCNJ5. Among 223 unilateral primary aldosteronism (uPA) individuals with a KCNJ5 mutation, we identified 6 adenomas with a KCNJ5 p.Gly387Arg (G387R) mutation, previously unreported in uPA patients. The 6 uPA patients harboring mutant KCNJ5-G387R were older, had a longer hypertensive history, and milder elevated preoperative plasma aldosterone levels than those APA patients with more frequently detected KCNJ5 mutations. CYP11B2 immunohistochemical staining was only positive in 3 adenomas, while the other 3 had co-existing multiple aldosterone-producing micronodules). The bioinformatics analysis predicted that function of the KCNJ5-G387R mutant channel could be pathological. However, the electrophysiological experiment demonstrated that transfected G387R mutant cells did not have an aberrantly stimulated ion current, with lower CYP11B2 synthesis and aldosterone production, when compared to that of the more frequently detected mutant KCNJ5-L168R transfected cells. In conclusion, mutant KCNJ5-G387R is not a functional KCNJ5 mutation in unilateral PA, and its associated only mildly elevated aldosterone expression actually dampened the clinical identification of clinical unilateral PA, in comparison to other KCNJ5 mutations. The KCNJ5-G387R mutation needs to be distinguished from functional KCNJ5 mutations during genomic analysis in APA evaluation because of its functional silence.
    Date: 2021-11
    Relation: Journal of Molecular Endocrinology. 2021 Nov;67(4):203-215.
    Link to: http://dx.doi.org/10.1530/jme-20-0282
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=0952-5041&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000704611700004
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85116764268
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