Skip navigation
Please use this identifier to cite or link to this item: http://repositorio2.unb.br/jspui/handle/10482/41115
Files in This Item:
There are no files associated with this item.
Title: Melittin sensitizes skin squamous carcinoma cells to 5-fluorouracil by affecting cell proliferation and survival
Authors: Ombredane, Alicia Simalie
Andrade, Laise Rodrigues de
Bonadio, Raphael Severino
Pinheiro, Willie Oliveira
Azevedo, Ricardo Bentes de
Joanitti, Graziella Anselmo
Assunto:: 5-fluorouracil
Melitina
Pele - câncer
Carcinoma de células escamosas
Issue Date: Feb-2021
Publisher: John Wiley & Sons Ltd
Citation: OMBREDANE, Alicia S. et al. Melittin sensitizes skin squamous carcinoma cells to 5-fluorouracil by affecting cell proliferation and survival. Experimental Dermatology, v. 30, n. 5, p. 710-716, 2021. DOI: https://doi.org/10.1111/exd.14289.
Abstract: Combined 5-fluorouracil (5-FU) and melittin (MEL) is believed to enhance cytotoxic effects on skin squamous cell carcinoma (SCC). However, the rationale underlying cytotoxicity is fundamentally important for a proper design of combination chemotherapy, and to provide translational insights for future therapeutics in the dermatology field. The aim was to elucidate the effects of 5-FU/MEL combination on the viability, proliferation and key structures of human squamous cell carcinoma (A431). Morphology, plasma membrane, DNA, mitochondria, oxidative stress, cell viability, proliferation and cell death pathways were targeted for investigation by microscopy, MTT, trypan blue assay, flow cytometry and real-time cell analysis. 5-FU/MEL (0.25 µM/0.52 µM) enhanced the cytotoxic effect in A431 cells (74.46%, p < .001) after 72 h exposure, showing greater cytotoxic effect when compared to each isolated compound (45.55% 5-FU and 61.78% MEL). The results suggest that MEL induces plasma membrane alterations that culminate in a loss of integrity at subsequent times, sensitizing the cell to 5-FU action. DNA fragmentation, S and G2/M arrest, disruption of mitochondrial metabolism, and alterations in cell morphology culminated in proliferation blockage and apoptosis. 5-FU/MEL combination design optimizes the cytotoxic effects of each drug at lower concentrations, which may represent an innovative strategy for SCC therapy.
DOI: https://doi.org/10.1111/exd.14289
metadata.dc.relation.publisherversion: https://onlinelibrary.wiley.com/doi/epdf/10.1111/exd.14289
Appears in Collections:Artigos publicados em periódicos e afins

Show full item record " class="statisticsLink btn btn-primary" href="/jspui/handle/10482/41115/statistics">



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.