“…[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. [1][2][3][6][7][8][9][10] Given that SR-BI plays an important role in lipid metabolism and atherosclerosis pathogenesis, the development of new anti-atherosclerotic drugs for the treatment and prevention of cardiovascular disease using SR-BI as the target has aroused widespread attention. 3,7,9,11,15 The posttranscriptional level of gene regulation is one of the main features of regulation of eukaryotic gene expression.…”