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Title: The Akt-like kinase of Leishmania panamensis: As a new molecular target for drug discovery
Authors: Tirado-Duarte, Didier
Marín-Villa, Marcel
Ochoa, Rodrigo
Blandón-Fuentes, Gustavo
Soares, Maurílio José
Robledo, Sara María
Varela-M, R. E.
Keywords: Akt protein;Apoptosis;Docking;Kinase inhibitors;L. panamensis;Animals;Drug Discovery;Humans;Leishmania guyanensis;Macrophages;Protein-Serine-Threonine Kinases;amphotericin B;ubmc 1;ubmc 4;unclassified drug;Enzyme;Parasites;Flagellum;IC50;Nonhuman;Chemistry
Issue Date: 1-Jan-2018
Publisher: Elsevier B.V.
Abstract: The Akt-like kinase of Leishmania spp. is a cytoplasmic orthologous protein of the serine/threonine kinase B-PKB/human-Akt group, which is involved in the cellular survival of these parasites. By the application of a computational strategy we obtained two specific inhibitors of the Akt-like protein of L. panamensis (UBMC1 and UBMC4), which are predicted to bind specifically to the pleckstrin domain (PH) of the enzyme. We show that the Akt-like of Leishmania panamensis is phospho-activated in parasites under nutritional and thermic stress, this phosphorylation is blocked by the UBMC1 and UMBC2 and such inhibition leads to cell death. Amongst the effects caused by the inhibitors on the parasites we found high percentage of hypodiploidy and loss of mitochondrial membrane potential. Ultrastructural studies showed highly vacuolated cytoplasm, as well as shortening of the flagellum, loss of nuclear membrane integrity and DNA fragmentation. Altogether the presented results suggest that the cell death caused by UMBC1 and UMBC4 may be associated to an apoptosis-like process. The compounds present an inhibitory concentration (IC50) over intracellular amastigotes of L. panamensis of 9.2 ± 0.8 μM for UBMC1 and 4.6 ± 1.9 μM for UBMC4. The cytotoxic activity for UBMC1 and UBMC4 in human macrophages derived from monocytes (huMDM) was 29 ± 1.2 μM and >40 μM respectively. Our findings strongly support that the presented compounds can be plausible candidates as a new therapeutic alternative for the inhibition of specific kinases of the parasite. © 2017 The Authors
ISSN: 0001706X
Appears in Collections:Artículos Científicos

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