Novel Peptide–Drug Conjugates with Dual Anticancer Activity

Cationic antimicrobial peptides (AMPs), also called host defence peptides, have established antimicrobial and anticancer activities. Conjugation of an AMP to a bioactive molecule with complementary activity can address some of the clinical limitations of the peptide candidate. This approach has been particularly applied in antimicrobial applications of AMPs, but it remains relatively less explored in the generation of anticancer candidates. In this study, two usnic acid derivatives, based on hydrazinothiazole and benzylidenefuranone pharmacophore moieties, respectively, were conjugated to L-K6, a lysine/leucine-rich AMP, through a new pyrazole ligation intrinsically driven by the cargo molecule. Both components, the usnic acid derivative and the peptide, are selectively active against cancer cells, by targeting the human DNA repair enzyme tyrosyl-DNA phosphodiesterase 1 (TDP1) and through DNA damage, respectively. The two conjugates, based on a hydrazone linkage, exhibited pleiotropic effects, ranging from reduction in the activity of the parent drugs to their conservation or even enhancement. Notably, the conjugates retained some anti-TDP1 activity and displayed intermediate, or even higher, cytotoxicities against glioblastoma cells, compared to their individual components.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2024-11-19
DOI
https://doi.org/10.3390/ijms252212411
Citations
2
Primary Topic
Chemical Synthesis and Analysis
Type
article
Field-Weighted Citation Impact
0.47

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article

Novel Peptide–Drug Conjugates with Dual Anticancer Activity

Olga I. Lavrik, Jérôme Leprince, Nadezhda S. Dyrkheeva, Siobhán O’Flaherty et al.
2 citations
International Journal of Molecular Sciences
Chemical Synthesis and Analysis
0.47
article

Novel Peptide–Drug Conjugates with Dual Anticancer Activity

Olga I. Lavrik, Jérôme Leprince, Nadezhda S. Dyrkheeva, Siobhán O’Flaherty, Mihayl Varbanov, Olga A. Luzina, Константин П. Волчо, Аndrey G. Pokrovsky, Нариман Ф. Салахутдинов, Marc Devocelle, Ysaline Krier, Alexandra L. Zakharenko
article en
2 citations

Abstract

Cationic antimicrobial peptides (AMPs), also called host defence peptides, have established antimicrobial and anticancer activities. Conjugation of an AMP to a bioactive molecule with complementary activity can address some of the clinical limitations of the peptide candidate. This approach has been particularly applied in antimicrobial applications of AMPs, but it remains relatively less explored in the generation of anticancer candidates. In this study, two usnic acid derivatives, based on hydrazinothiazole and benzylidenefuranone pharmacophore moieties, respectively, were conjugated to L-K6, a lysine/leucine-rich AMP, through a new pyrazole ligation intrinsically driven by the cargo molecule. Both components, the usnic acid derivative and the peptide, are selectively active against cancer cells, by targeting the human DNA repair enzyme tyrosyl-DNA phosphodiesterase 1 (TDP1) and through DNA damage, respectively. The two conjugates, based on a hydrazone linkage, exhibited pleiotropic effects, ranging from reduction in the activity of the parent drugs to their conservation or even enhancement. Notably, the conjugates retained some anti-TDP1 activity and displayed intermediate, or even higher, cytotoxicities against glioblastoma cells, compared to their individual components.

International Journal of Molecular SciencesVol. 25(22)
Centre National de la Recherche Scientifique (FR), Inserm (FR), Novosibirsk State University (RU), Institute of Chemical Biology and Fundamental Medicine (RU), Novosibirsk Institute of Organic Chemistry (RU), Normandie Université (FR), Siberian Branch of the Russian Academy of Sciences (RU), Laboratoire Lorrain de Chimie Moléculaire (FR), Université de Rouen Normandie (FR), Université de Lorraine (FR)
Science Foundation Ireland, Ministry of Science and Higher Education of the Russian Federation
Openalex Percentile: Top 34%
Chemical Synthesis and Analysis
0.47
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