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The V369M Gcgr Knock-in Mice Are a Precision Medicine Model of Mild Mahvash Disease

Overview
Journal Biochem J
Specialty Biochemistry
Date 2020 Aug 14
PMID 32785645
Citations 2
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Abstract

The detailed metabolic characterization of the glucagon receptor (Gcgr)V369M+/+ mutant mice described in Lin et al. in the Biochemical Journal is of interest and resulting in the expected metabolic profile. We would like to point out that these mice might also be extremely useful as a precision medicine model of mild Mahvash disease, a rare hereditary pancreatic neuroendocrine tumor syndrome characterized by inactivating mutations in the glucagon receptor. Further characterization of pancreas morphology and histology in the GcgrV369M+/+ mice at more advanced ages will be critically important to understand mild Mahvash disease in humans.

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PMID: 35784565 PMC: 9243425. DOI: 10.3389/fendo.2022.928016.


Deleterious mutation V369M in the mouse GCGR gene causes abnormal plasma amino acid levels indicative of a possible liver-α-cell axis.

Liu Q, Lin G, Chen Y, Feng W, Xu Y, Lyu J Biosci Rep. 2021; 41(6).

PMID: 34002801 PMC: 8173527. DOI: 10.1042/BSR20210758.