Crotalicidin and NA-CATH-ATRA-1-ATRA-1 peptide-induced membrane disruption in human breast cancer cells

Cationic peptides offer a promising alternative for cancer treatment due to their ability to target cancer cells via standard membrane features, thereby overcoming intratumoral heterogeneity. This study investigates the cytotoxic activity and the membrane-disruptive effects of two snake venom-derive...

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Autores:
Gallego Londoño, Vanessa
Santa González, Gloria Angélica
Giraldo Lorza, Juan Manuel
Rojas López, Mauricio
Manrique Moreno, Marcela María
Wisman, G. Bea A.
Jong, Steven de
Tipo de recurso:
Article of investigation
Fecha de publicación:
2025
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/46545
Acceso en línea:
https://hdl.handle.net/10495/46545
Palabra clave:
Peptidos
Peptides
Neoplasias de mama
Breast Neoplasms
Citotoxinas
Cytotoxins
Permeabilidad de la Membrana Celular
Cell Membrane Permeability
Snake Venoms - pharmacology
Venenos de serpiente - farmacología
http://id.nlm.nih.gov/mesh/D010455
http://id.nlm.nih.gov/mesh/D001943
http://id.nlm.nih.gov/mesh/D003603
http://id.nlm.nih.gov/mesh/D002463
http://id.nlm.nih.gov/mesh/D012910
ODS 3: Salud y bienestar. Garantizar una vida sana y promover el bienestar de todos a todas las edades
Rights
openAccess
License
http://creativecommons.org/licenses/by/4.0/
Description
Summary:Cationic peptides offer a promising alternative for cancer treatment due to their ability to target cancer cells via standard membrane features, thereby overcoming intratumoral heterogeneity. This study investigates the cytotoxic activity and the membrane-disruptive effects of two snake venom-derived peptides, Crotalicidin (Ctn) and NA-CATH-ATRA-1-ATRA-1 (NA) in human breast cancer cells. Cell viability assays showed that both Ctn and NA significantly diminished the viability of MCF-7 and MDA-MB-231 cells, with NA showing greater potency, as indicated by lower IC50 values of 13.4 μM for MCF-7 and 6.4 μM for MDA-MB-231. Microscopy and flow cytometry revealed size reduction and increased granularity in treated cells. Further analyses indicated that the peptides induced membrane permeabilization, as evidenced by significant propidium iodide uptake, without significantly altering mitochondrial membrane potential. Apoptosis markers such as cleaved caspase-9 and PARP, were not detected by western blot. Additionally, LDH release and confocal microscopic analysis supported the findings of membrane disruption. Finally, infrared spectroscopy (FT-IR) on lipid extracts revealed peptide-membrane interactions, resulting in phase transitions consistent with membrane disruption. These findings highlight the potent cytotoxic effects of Ctn and NA on breast cancer cells and their potential as novel therapeutic agents.