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Human Resistin and the RELM of Inflammation in Diabesity

Overview
Publisher Biomed Central
Specialty Endocrinology
Date 2015 Jun 23
PMID 26097512
Citations 16
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Abstract

The initial discovery of resistin and resistin-like molecules (RELMs) in rodents suggested a role for these adipocytokines in molecular linkage of obesity, Type 2 Diabetes mellitus and metabolic syndrome. Since then, it became apparent that the story of resistin and RELMs was very much of mice and men. The putative role of this adipokine family evolved from that of a conveyor of insulin resistance in rodents to instigator of inflammatory processes in humans. Structural dissimilarity, variance in distribution profiles and a lack of corroborating evidence for functional similarities separate the biological functions of resistin in humans from that of rodents. Although present in gross visceral fat deposits in humans, resistin is a component of inflammation, being released from infiltrating white blood cells of the sub-clinical chronic low grade inflammatory response accompanying obesity, rather than from the adipocyte itself. This led researchers to further explore the functions of the resistin family of proteins in inflammatory-related conditions such as atherosclerosis, as well as in cancers such as endometrial and gastric cancers. Although elevated levels of resistin have been found in these conditions, whether it is causative or as a result of these conditions still remains to be determined.

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References
1.
Yang R, Huang Q, Xu A, McLenithan J, Eisen J, Shuldiner A . Comparative studies of resistin expression and phylogenomics in human and mouse. Biochem Biophys Res Commun. 2003; 310(3):927-35. DOI: 10.1016/j.bbrc.2003.09.093. View

2.
Osawa H, Tabara Y, Kawamoto R, Ohashi J, Ochi M, Onuma H . PPARgamma Pro12Ala Pro/Pro and resistin SNP-420 G/G genotypes are synergistically associated with plasma resistin in the Japanese general population. Clin Endocrinol (Oxf). 2009; 71(3):341-5. DOI: 10.1111/j.1365-2265.2008.03465.x. View

3.
Delhanty P, Mesotten D, McDougall F, Baxter R . Growth hormone rapidly induces resistin gene expression in white adipose tissue of spontaneous dwarf (SDR) rats. Endocrinology. 2002; 143(6):2445-8. DOI: 10.1210/endo.143.6.8947. View

4.
Ouchi N, Parker J, Lugus J, Walsh K . Adipokines in inflammation and metabolic disease. Nat Rev Immunol. 2011; 11(2):85-97. PMC: 3518031. DOI: 10.1038/nri2921. View

5.
Feve B, Bastard J . The role of interleukins in insulin resistance and type 2 diabetes mellitus. Nat Rev Endocrinol. 2009; 5(6):305-11. DOI: 10.1038/nrendo.2009.62. View