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Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk

Metastatic melanoma is an aggressive cancer with increasing incidence and limited therapies in advanced stages. Systemic neutrophilia or abundant neutrophils in the tumor contribute toward its worst prognosis, and the interplay of cancer and the immune system has been shown in tumor development and...

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Autores principales: Drewes, Carine C, Alves, Aline de CS, Hebeda, Cristina B, Copetti, Isabela, Sandri, Silvana, Uchiyama, Mayara K, Araki, Koiti, Guterres, Silvia S, Pohlmann, Adriana R, Farsky, Sandra H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627757/
https://www.ncbi.nlm.nih.gov/pubmed/29026308
http://dx.doi.org/10.2147/IJN.S140557
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author Drewes, Carine C
Alves, Aline de CS
Hebeda, Cristina B
Copetti, Isabela
Sandri, Silvana
Uchiyama, Mayara K
Araki, Koiti
Guterres, Silvia S
Pohlmann, Adriana R
Farsky, Sandra H
author_facet Drewes, Carine C
Alves, Aline de CS
Hebeda, Cristina B
Copetti, Isabela
Sandri, Silvana
Uchiyama, Mayara K
Araki, Koiti
Guterres, Silvia S
Pohlmann, Adriana R
Farsky, Sandra H
author_sort Drewes, Carine C
collection PubMed
description Metastatic melanoma is an aggressive cancer with increasing incidence and limited therapies in advanced stages. Systemic neutrophilia or abundant neutrophils in the tumor contribute toward its worst prognosis, and the interplay of cancer and the immune system has been shown in tumor development and metastasis. We recently showed the in vivo efficacy of poly(ε-caprolactone) lipid-core nanocapsule (LNC) or LNC loaded with acetyleugenol (AcE-LNC) to treat B16F10-induced melanoma in mice. In this study, we investigated whether LNC or AcE-LNC toxicity could involve modifications on crosstalk of melanoma cells and neutrophils. Therefore, melanoma cells (B16F10) were pretreated with vehicle, LNC, AcE or AcE-LNC for 24 h, washed and, further, cocultured for 18 h with peritoneal neutrophils obtained from C57Bl/6 mice. Melanoma cells were able to internalize the LNC or AcE-LNC after 2 h of incubation. LNC or AcE-LNC pretreatments did not cause melanoma cells death, but led melanoma cells to be more susceptible to death in serum deprivation or hypoxia or in the presence of neutrophils. Interestingly, the production of reactive oxygen species (ROS), which causes cell death, was increased by neutrophils in the presence of LNC- and AcE-LNC-pretreated melanoma cells. LNC or AcE-LNC treatments reduced the concentration of transforming growth factor-β (TGF-β) in the supernatant of melanoma cells, a known factor secreted by cancer cells to induce pro-tumoral actions of neutrophils in the tumor microenvironment. In addition, we found reduced levels of pro-tumoral chemical mediators VEGF, arginase-1, interleukin-10 (IL-10) and matrix metalloproteinase-9 (MMP-9) in the supernatant of LNC or AcE-LNC-pretreated melanoma cells and cocultured with neutrophils. Overall, our data show that the uptake of LNC or AcE-LNC by melanoma cells affects intracellular mechanisms leading to more susceptibility to death and also signals higher neutrophil antitumoral activity.
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spelling pubmed-56277572017-10-12 Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk Drewes, Carine C Alves, Aline de CS Hebeda, Cristina B Copetti, Isabela Sandri, Silvana Uchiyama, Mayara K Araki, Koiti Guterres, Silvia S Pohlmann, Adriana R Farsky, Sandra H Int J Nanomedicine Original Research Metastatic melanoma is an aggressive cancer with increasing incidence and limited therapies in advanced stages. Systemic neutrophilia or abundant neutrophils in the tumor contribute toward its worst prognosis, and the interplay of cancer and the immune system has been shown in tumor development and metastasis. We recently showed the in vivo efficacy of poly(ε-caprolactone) lipid-core nanocapsule (LNC) or LNC loaded with acetyleugenol (AcE-LNC) to treat B16F10-induced melanoma in mice. In this study, we investigated whether LNC or AcE-LNC toxicity could involve modifications on crosstalk of melanoma cells and neutrophils. Therefore, melanoma cells (B16F10) were pretreated with vehicle, LNC, AcE or AcE-LNC for 24 h, washed and, further, cocultured for 18 h with peritoneal neutrophils obtained from C57Bl/6 mice. Melanoma cells were able to internalize the LNC or AcE-LNC after 2 h of incubation. LNC or AcE-LNC pretreatments did not cause melanoma cells death, but led melanoma cells to be more susceptible to death in serum deprivation or hypoxia or in the presence of neutrophils. Interestingly, the production of reactive oxygen species (ROS), which causes cell death, was increased by neutrophils in the presence of LNC- and AcE-LNC-pretreated melanoma cells. LNC or AcE-LNC treatments reduced the concentration of transforming growth factor-β (TGF-β) in the supernatant of melanoma cells, a known factor secreted by cancer cells to induce pro-tumoral actions of neutrophils in the tumor microenvironment. In addition, we found reduced levels of pro-tumoral chemical mediators VEGF, arginase-1, interleukin-10 (IL-10) and matrix metalloproteinase-9 (MMP-9) in the supernatant of LNC or AcE-LNC-pretreated melanoma cells and cocultured with neutrophils. Overall, our data show that the uptake of LNC or AcE-LNC by melanoma cells affects intracellular mechanisms leading to more susceptibility to death and also signals higher neutrophil antitumoral activity. Dove Medical Press 2017-09-27 /pmc/articles/PMC5627757/ /pubmed/29026308 http://dx.doi.org/10.2147/IJN.S140557 Text en © 2017 Drewes et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Drewes, Carine C
Alves, Aline de CS
Hebeda, Cristina B
Copetti, Isabela
Sandri, Silvana
Uchiyama, Mayara K
Araki, Koiti
Guterres, Silvia S
Pohlmann, Adriana R
Farsky, Sandra H
Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
title Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
title_full Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
title_fullStr Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
title_full_unstemmed Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
title_short Role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
title_sort role of poly(ε-caprolactone) lipid-core nanocapsules on melanoma–neutrophil crosstalk
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5627757/
https://www.ncbi.nlm.nih.gov/pubmed/29026308
http://dx.doi.org/10.2147/IJN.S140557
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