2016
DOI: 10.1161/circulationaha.116.022593
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Can We Make High-Density Lipoproteins Great Again?

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Cited by 1 publication
(4 citation statements)
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“…[1][2][3][6][7][8] The treatment of atherosclerotic diseases targeting HDL and its relevant receptor has received widespread attention. [1][2][3][6][7][8][9][10] Human scavenger receptor class B, member 1 (SR-BI or SCARB1), also known as CD36 and lysosomal integral membrane protein II analogous 1 (CLA-1) in humans, is an important integral membrane glycoprotein of the scavenger receptor family. [1][2][3]11 SR-BI is mainly expressed in the liver, gastrointestinal tract, and steroidogenic organs or is detected in macrophages and endothelial cells.…”
Section: Introductionmentioning
confidence: 99%
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“…[1][2][3][6][7][8] The treatment of atherosclerotic diseases targeting HDL and its relevant receptor has received widespread attention. [1][2][3][6][7][8][9][10] Human scavenger receptor class B, member 1 (SR-BI or SCARB1), also known as CD36 and lysosomal integral membrane protein II analogous 1 (CLA-1) in humans, is an important integral membrane glycoprotein of the scavenger receptor family. [1][2][3]11 SR-BI is mainly expressed in the liver, gastrointestinal tract, and steroidogenic organs or is detected in macrophages and endothelial cells.…”
Section: Introductionmentioning
confidence: 99%
“…13,14 The key mechanism of HDL-C transport is the selective uptake of the cholesterol esters. [1][2][3][6][7][8][9][10] As a functional HDL receptor with high expression level in the liver, SR-BI binds with HDL to mediate the selective uptake of HDL-C with high affinity and high saturation, and this process is the final rate-limiting step of RCT. [1][2][3][4]6 The overexpression of hepatocyte SR-BI can indeed promote the reverse transport of HDL-C, enhance the HDL clearance rate in plasma, and reduce the morbidity and mortality of atherosclerosis and associated cardiovascular risk events.…”
Section: Introductionmentioning
confidence: 99%
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