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LRG1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

LRG1
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Leucine-rich alpha-2-glycoprotein 1 is a protein which in humans is encoded by the gene LRG1.[5]

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Function

The leucine-rich repeat (LRR) family of proteins, including LRG1, have been shown to be involved in protein-protein interaction, signal transduction, and cell adhesion and development. LRG1 is expressed during granulocyte differentiation.[5][6]

LRG1 has been shown to be involved in promoting neovascularization (new blood vessel growth) through causing a switch in transforming growth factor beta (TGFbeta) signaling in endothelial cells. LRG1 binds to the accessory receptor endoglin and promotes signaling via the ALK1-Smad1/5/8 pathway.[7]

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Application

Levels of the LRG protein are markedly elevated in acute appendicitis and therefore could be used as a diagnostic aid.[8]

LRG1 may be a potential therapeutic target for the treatment of diseases where there is aberrant neovascularization.[7]

Circulating LRG1 levels are increased in many cancer patients and may be a useful biomarker. Inhibition of LRG1 normalises the tumor vasculature, improves the efficacy of cytotoxic and immune therapies,[9] and restricts metastatic spread. [10]

LRG1 has been implicated in the pathogenesis of numerous diseases including cancer, eye disease, neurodegenerative disease, diabetes, lung and kidney disease[11]

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References

Further reading

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