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<title>Small molecule anion carriers facilitate lactate transport in model liposomes and cells</title>
<creator>Alonso Carrillo, Daniel</creator>
<creator>Arias Betancur, Alain</creator>
<creator>Carreira Barral, Israel</creator>
<creator>Fontova Pale, Pere</creator>
<creator>Soto Cerrato, Vanessa</creator>
<creator>García Valverde, María</creator>
<creator>Pérez Tomás, Ricardo</creator>
<creator>Quesada Pato, Roberto</creator>
<description>An excessive production of lactate by cancer cells fosters tumor growth and metastasis. Therefore, targeting lactate metabolism and transport offers a new therapeutic strategy against cancer, based on dependency of some cancer cells for lactate as energy fuel or as oncogenic signal. Herein we present a family of&#xd;
anionophores based on the structure of click-tambjamines that have proved to be extremely active lactate&#xd;
carriers across phospholipid membranes. Compound 1, the most potent lactate transmembrane carrier,&#xd;
was studied in HeLa cells. The use of a monocarboxylate transporters (MCTs) inhibitor proved that 1 is&#xd;
an active lactate transporter in living cells, confirming the results obtained in phospholipid vesicles. Moreover, an additive effect of compound 1 with cisplatin was observed in HeLa cells. Identification of active&#xd;
lactate anionophores working in living cells opens up ways to exploit this class of compounds as molecular&#xd;
tools and drugs addressing dysregulated lactate metabolism.</description>
<date>2024-02-07</date>
<date>2024-02-07</date>
<date>2023-09</date>
<type>info:eu-repo/semantics/article</type>
<identifier>2589-0042</identifier>
<identifier>http://hdl.handle.net/10259/8608</identifier>
<identifier>10.1016/j.isci.2023.107898</identifier>
<language>eng</language>
<relation>iScience. 2023, V. 26, n. 10, 107898</relation>
<relation>https://doi.org/10.1016/j.isci.2023.107898</relation>
<rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</rights>
<rights>info:eu-repo/semantics/openAccess</rights>
<rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</rights>
<publisher>Elsevier</publisher>
</thesis></metadata></record></GetRecord></OAI-PMH>