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Cholesin is a hormone produced by the intestine in response to dietary cholesterol absorption. Its main function is to inhibit cholesterol synthesis in the liver, helping maintain cholesterol homeostasis[3][4][5]. Cholesin exerts its effect by binding to the GPR146 receptor, serving as a key regulator of plasma cholesterol in mammals. The hormone is a product of the *CHLSN* gene (also known as C7orf50). Cholesin’s activity includes suppressing VLDL secretion from hepatocytes, and its expression is upregulated during high-cholesterol diets. As a newly described molecule, it is considered a promising therapeutic target for atherosclerosis and hypercholesterolemia, and it may serve as a biomarker for cholesterol absorption and homeostasis[3][4][5]. If more granular molecular descriptors (sequence, structure, motifs) are needed, C7orf50 encodes a small (22 kDa), basic (pI 9.7) peptide with conserved but largely uncharacterized functional domains, mainly localized to the nucleus and extracellular space[1][4]. There is no evidence of misspelling or incorrect identity; the nomenclature matches the latest literature and databases. Its main role is as a hormone, not a traditional receptor or enzyme; it acts upon a target receptor (GPR146). Current knowledge is limited, but valid and scientifically grounded.
Cholesin binds to GPR146 on hepatic cells, leading to inhibition of cholesterol synthesis and decreased VLDL (very low-density lipoprotein) secretion, reducing circulating cholesterol levels[3][4].
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