Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells

ABSTRACT: Melanoma is the most dangerous and lethal form of skin cancer, due to its ability to spread to different organs if it is not treated at an early stage. Conventional chemotherapeutics are failing as a result of drug resistance and weak tumor selectivity. Therefore, efforts to evaluate novel...

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Autores:
Patiño González, Edwin Bairon
Santa González, Gloria Angélica
Manrique Moreno, Marcela María
Tipo de recurso:
Article of investigation
Fecha de publicación:
2020
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/35178
Acceso en línea:
https://hdl.handle.net/10495/35178
Palabra clave:
Melanoma
Puntos de control del ciclo celular
Cell Cycle Checkpoints
Péptidos Antimicrobianos
Antimicrobial Peptides
Neoplasias Cutáneas
Skin Neoplasms
Muerte Celular
Cell Death
Membrana Celular
Cell Membrane
Rights
openAccess
License
http://creativecommons.org/licenses/by/2.5/co/
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dc.title.spa.fl_str_mv Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
title Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
spellingShingle Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
Melanoma
Puntos de control del ciclo celular
Cell Cycle Checkpoints
Péptidos Antimicrobianos
Antimicrobial Peptides
Neoplasias Cutáneas
Skin Neoplasms
Muerte Celular
Cell Death
Membrana Celular
Cell Membrane
title_short Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
title_full Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
title_fullStr Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
title_full_unstemmed Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
title_sort Synthetic Peptide ∆M4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells
dc.creator.fl_str_mv Patiño González, Edwin Bairon
Santa González, Gloria Angélica
Manrique Moreno, Marcela María
dc.contributor.author.none.fl_str_mv Patiño González, Edwin Bairon
Santa González, Gloria Angélica
Manrique Moreno, Marcela María
dc.contributor.researchgroup.spa.fl_str_mv Grupo de Bioquímica Estructural de Macromoléculas
dc.subject.decs.none.fl_str_mv Melanoma
Puntos de control del ciclo celular
Cell Cycle Checkpoints
Péptidos Antimicrobianos
Antimicrobial Peptides
Neoplasias Cutáneas
Skin Neoplasms
Muerte Celular
Cell Death
Membrana Celular
Cell Membrane
topic Melanoma
Puntos de control del ciclo celular
Cell Cycle Checkpoints
Péptidos Antimicrobianos
Antimicrobial Peptides
Neoplasias Cutáneas
Skin Neoplasms
Muerte Celular
Cell Death
Membrana Celular
Cell Membrane
description ABSTRACT: Melanoma is the most dangerous and lethal form of skin cancer, due to its ability to spread to different organs if it is not treated at an early stage. Conventional chemotherapeutics are failing as a result of drug resistance and weak tumor selectivity. Therefore, efforts to evaluate novel molecules for the treatment of skin cancer are necessary. Antimicrobial peptides have become attractive anticancer agents because they execute their biological activity with features such as a high potency of action, a wide range of targets, and high target specificity and selectivity. In the present study, the antiproliferative activity of the synthetic peptide ∆M4 on A375 human melanoma cells and spontaneously immortalized HaCaT human keratinocytes was investigated. The cytotoxic effect of ∆M4 treatment was evaluated through propidium iodide uptake by flow cytometry. The results indicated selective toxicity in A375 cells and, in order to further investigate the mode of action, assays were carried out to evaluate morphological changes, mitochondrial function, and cell cycle progression. The findings indicated that ∆M4 exerts its antitumoral effects by multitarget action, causing cell membrane disruption, a change in the mitochondrial transmembrane potential, an increase of reactive oxygen species, and cell cycle accumulation in S-phase. Further exploration of the peptide may be helpful in the design of novel anticancer peptides.
publishDate 2020
dc.date.issued.none.fl_str_mv 2020
dc.date.accessioned.none.fl_str_mv 2023-05-31T15:43:33Z
dc.date.available.none.fl_str_mv 2023-05-31T15:43:33Z
dc.type.spa.fl_str_mv Artículo de investigación
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dc.identifier.citation.spa.fl_str_mv Santa-González GA, Patiño-González E, Manrique-Moreno M. Synthetic Peptide ΔM4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells. Molecules. 2020 Dec 2;25(23):5684. doi: 10.3390/molecules25235684.
dc.identifier.issn.none.fl_str_mv 1420-3049
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/35178
dc.identifier.doi.none.fl_str_mv 10.3390/molecules25235684
identifier_str_mv Santa-González GA, Patiño-González E, Manrique-Moreno M. Synthetic Peptide ΔM4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells. Molecules. 2020 Dec 2;25(23):5684. doi: 10.3390/molecules25235684.
1420-3049
10.3390/molecules25235684
url https://hdl.handle.net/10495/35178
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Molecules
dc.relation.citationendpage.spa.fl_str_mv 15
dc.relation.citationissue.spa.fl_str_mv 5684
dc.relation.citationstartpage.spa.fl_str_mv 1
dc.relation.citationvolume.spa.fl_str_mv 25
dc.relation.ispartofjournal.spa.fl_str_mv Molecules
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institution Universidad de Antioquia
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spelling Patiño González, Edwin BaironSanta González, Gloria AngélicaManrique Moreno, Marcela MaríaGrupo de Bioquímica Estructural de Macromoléculas2023-05-31T15:43:33Z2023-05-31T15:43:33Z2020Santa-González GA, Patiño-González E, Manrique-Moreno M. Synthetic Peptide ΔM4-Induced Cell Death Associated with Cytoplasmic Membrane Disruption, Mitochondrial Dysfunction and Cell Cycle Arrest in Human Melanoma Cells. Molecules. 2020 Dec 2;25(23):5684. doi: 10.3390/molecules25235684.1420-3049https://hdl.handle.net/10495/3517810.3390/molecules25235684ABSTRACT: Melanoma is the most dangerous and lethal form of skin cancer, due to its ability to spread to different organs if it is not treated at an early stage. Conventional chemotherapeutics are failing as a result of drug resistance and weak tumor selectivity. Therefore, efforts to evaluate novel molecules for the treatment of skin cancer are necessary. Antimicrobial peptides have become attractive anticancer agents because they execute their biological activity with features such as a high potency of action, a wide range of targets, and high target specificity and selectivity. In the present study, the antiproliferative activity of the synthetic peptide ∆M4 on A375 human melanoma cells and spontaneously immortalized HaCaT human keratinocytes was investigated. The cytotoxic effect of ∆M4 treatment was evaluated through propidium iodide uptake by flow cytometry. The results indicated selective toxicity in A375 cells and, in order to further investigate the mode of action, assays were carried out to evaluate morphological changes, mitochondrial function, and cell cycle progression. The findings indicated that ∆M4 exerts its antitumoral effects by multitarget action, causing cell membrane disruption, a change in the mitochondrial transmembrane potential, an increase of reactive oxygen species, and cell cycle accumulation in S-phase. 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