The progression of metastatic melanoma augments a pro-oxidative milieu locally but not systemically.


Journal

Pathology, research and practice
ISSN: 1618-0631
Titre abrégé: Pathol Res Pract
Pays: Germany
ID NLM: 7806109

Informations de publication

Date de publication:
Nov 2020
Historique:
received: 25 06 2020
revised: 14 09 2020
accepted: 15 09 2020
pubmed: 2 10 2020
medline: 9 9 2021
entrez: 1 10 2020
Statut: ppublish

Résumé

Malignant melanoma is the most dangerous form of skin cancer. Despite new therapies for melanoma treatment, effective therapy is mainly limited by excessive metastasis. Currently, the factors determining metastasis development are not elucidated, but oxidative stress was suggested to be involved. To this end, we analyzed oxidative stress parameters during the metastatic development using the syngeneic B16F10 melanoma model. An increase in blood plasma lipid peroxidation occurred at the earliest stage of the disease, with a progressive decrease in oxidative damage and an increase in antioxidant defense. Vice versa, increased lipid peroxidation and 3-nitrotyrosine, and decreased antioxidant parameters were observed in the metastatic nodules throughout the disease. This was concomitant with a progressive increase in vascular endothelial growth factor and proliferating cell nuclear antigen. We conclude that the oxidative stress in the bloodstream decreases during the metastatic process and that nitrosative stress increases during the proliferation and growth of metastatic nodules in the tumor microenvironment. These results will help to better understand the role of oxidative stress during melanoma metastasis.

Identifiants

pubmed: 33002848
pii: S0344-0338(20)32073-2
doi: 10.1016/j.prp.2020.153218
pii:
doi:

Substances chimiques

Reactive Nitrogen Species 0
Reactive Oxygen Species 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

153218

Informations de copyright

Copyright © 2020 Elsevier GmbH. All rights reserved.

Auteurs

Gabriella Pasqual-Melo (G)

Laboratory of Molecular Pathology, State University of Londrina, Brazil; Laboratory of Pathophysiology and Free Radicals, State University of Londrina, Brazil; ZIK Plasmatis, Leibniz Institute for Plasma Science and Technology (INP), Greifswald, Germany.

Sara S Bernardes (SS)

Laboratory of Molecular Pathology, State University of Londrina, Brazil; Laboratory of Tissue Microenvironment, Federal University of Minas Gerais, Brazil.

Fernando P Souza-Neto (FP)

Laboratory of Molecular Pathology, State University of Londrina, Brazil; Laboratory of Pathophysiology and Free Radicals, State University of Londrina, Brazil.

Iriana M Carrara (IM)

Laboratory of Molecular Pathology, State University of Londrina, Brazil; Laboratory of Pathophysiology and Free Radicals, State University of Londrina, Brazil.

Leandra N Z Ramalho (LNZ)

Department of Pathology and Legal Medicine, University of São Paulo, Brazil.

Poliana C Marinello (PC)

Laboratory of Molecular Pathology, State University of Londrina, Brazil.

Rodrigo C Luiz (RC)

Laboratory of Molecular Pathology, State University of Londrina, Brazil.

Rubens Cecchini (R)

Laboratory of Pathophysiology and Free Radicals, State University of Londrina, Brazil.

Sander Bekeschus (S)

ZIK Plasmatis, Leibniz Institute for Plasma Science and Technology (INP), Greifswald, Germany.

Alessandra L Cecchini (AL)

Laboratory of Molecular Pathology, State University of Londrina, Brazil; Laboratory of Pathophysiology and Free Radicals, State University of Londrina, Brazil. Electronic address: alcecchini@uel.br.

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Classifications MeSH