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Targeting solute carriers to modulate receptor–ligand interactions

Trends in Pharmacological Sciences, vol. 43, pp. 358–361

Abstract

Solute carrier transporters (SLCs) limit receptor activation via uptake of extracellular ligands. Novel concepts are emerging that describe the modulation of intracellular and plasma membrane receptors by ligand influx and efflux via SLCs, respectively. Here, we evaluate recent insights and provide an outlook for developing potential therapeutic strategies.

Authors 4

  1. Leiden University

    Affiliation as printed

    Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands

  2. Austrian Academy of Sciences · Medical University of Vienna · CeMM Research Center for Molecular Medicine

    Affiliation as printed

    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Medical University of Vienna, 1090 Vienna, Austria; Center for Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria

    CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Medical University of Vienna, 1090 Vienna, Austria

    Center for Physiology and Pharmacology, Medical University of Vienna, 1090 Vienna, Austria

  3. Leiden University

    Affiliation as printed

    Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands

  4. Leiden University · Oncode Institute

    Affiliation as printed

    Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands; Oncode Institute, Leiden, The Netherlands. Electronic address: l.h.heitman@lacdr.leidenuniv.nl

    Division of Drug Discovery and Safety, Leiden Academic Centre for Drug Research (LACDR), Leiden University, Leiden, The Netherlands

    Oncode Institute, Leiden, The Netherlands

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References 15

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