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Nutrient transporters are a vast and diverse class of membrane-bound proteins, primarily comprising the Solute Carrier (SLC) and ATP-binding cassette (ABC) superfamilies, that facilitate the movement of essential molecules such as glucose, amino acids, ions, and vitamins across biological membranes [1][2]. These proteins are fundamental to maintaining cellular homeostasis, providing the necessary substrates for energy production, biosynthesis, and signaling [3]. In various pathological states, particularly cancer, nutrient transporters are often dysregulated or overexpressed to support the high metabolic demands of rapid cell proliferation, a phenomenon known as metabolic reprogramming [4]. Therapeutic strategies involve the use of small molecule inhibitors to starve diseased cells of essential nutrients or to modulate systemic levels of metabolites, as seen with SGLT2 inhibitors in the treatment of type 2 diabetes [5]. Despite their therapeutic potential, the broad expression patterns of many nutrient transporters across different tissues present significant challenges regarding selectivity and the risk of systemic side effects [6].
Nutrient transporters are targeted through various mechanisms, most commonly via competitive inhibition where a drug mimics the natural substrate to block the transport pore, or non-competitive inhibition where the drug binds to an allosteric site to prevent conformational changes necessary for translocation [3][5].
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