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BLT-1 (Block Lipid Transport 1) is a potent, small-molecule inhibitor of Scavenger Receptor Class B Type 1 (SR-B1). SR-B1 is a multi-functional membrane receptor that facilitates the selective uptake of cholesteryl esters from high-density lipoprotein (HDL) into cells. In the context of oncology, BLT-1 is being investigated for its ability to disrupt lipid metabolism in cancer cells, particularly triple-negative breast cancer (TNBC), where SR-B1 is often overexpressed to meet high metabolic demands. Preclinical studies have shown that the efficacy of BLT-1 is influenced by extracellular glucose levels and specific genetic polymorphisms in the SR-B1 gene (such as rs2293440), highlighting its potential role in personalized metabolic-targeted cancer therapy.
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