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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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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. |
format | Online Article Text |
id | pubmed-5627757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
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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