Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development
Autor(a) principal: | |
---|---|
Data de Publicação: | 2021 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFRGS |
Texto Completo: | http://hdl.handle.net/10183/233453 |
Resumo: | Introduction: Renal cell carcinoma (RCC) is one of the most prevalent kidney tumors. Inflammation is believed to be a key factor in its progression and spread since inflammatory markers are generally associated with poor prognosis in RCC patients. Cytokines are cell communication molecules involved in both healthy and pathological processes, including tumor growth and progression. Recent findings suggest that cytokine level measurements could be used for cancer monitoring and prognosis. Methods: This study characterized and compared the levels of different cytokines associated with the classical Th1, Th2, and Th17 immune responses in plasma samples from RCC patients (n = 25) and healthy controls (n = 29). Cytokine levels (IL-2, IL-4, IL-6, IL-10, TNF-α, IFN-γ, and IL-17A) were evaluated by flow cytometry using a BD Cytometric Bead Array (CBA) kit. Results: No statistical differences in systemic IL-2, IL-4, IL-10, IL-17A, TNF, and INF-γ levels were observed between RCC patients and controls (p > 0.05). However, higher systemic IL-6 levels were observed in RCC patients (p = 0.0034). Conclusions: This study highlights the importance of assessing the impact of IL-6 on RCC pathogenesis and its potential role as a biomarker of disease progression. |
id |
UFRGS-2_2cbc8d351f54d078833556076e4ac3db |
---|---|
oai_identifier_str |
oai:www.lume.ufrgs.br:10183/233453 |
network_acronym_str |
UFRGS-2 |
network_name_str |
Repositório Institucional da UFRGS |
repository_id_str |
|
spelling |
Cechim, GiovanaEllwanger, Joel HenriqueKaminski, Valéria de LimaBerger, MiltonChies, Jose Artur Bogo2021-12-29T04:27:19Z20212357-9730http://hdl.handle.net/10183/233453001134281Introduction: Renal cell carcinoma (RCC) is one of the most prevalent kidney tumors. Inflammation is believed to be a key factor in its progression and spread since inflammatory markers are generally associated with poor prognosis in RCC patients. Cytokines are cell communication molecules involved in both healthy and pathological processes, including tumor growth and progression. Recent findings suggest that cytokine level measurements could be used for cancer monitoring and prognosis. Methods: This study characterized and compared the levels of different cytokines associated with the classical Th1, Th2, and Th17 immune responses in plasma samples from RCC patients (n = 25) and healthy controls (n = 29). Cytokine levels (IL-2, IL-4, IL-6, IL-10, TNF-α, IFN-γ, and IL-17A) were evaluated by flow cytometry using a BD Cytometric Bead Array (CBA) kit. Results: No statistical differences in systemic IL-2, IL-4, IL-10, IL-17A, TNF, and INF-γ levels were observed between RCC patients and controls (p > 0.05). However, higher systemic IL-6 levels were observed in RCC patients (p = 0.0034). Conclusions: This study highlights the importance of assessing the impact of IL-6 on RCC pathogenesis and its potential role as a biomarker of disease progression.application/pdfengClinical and biomedical research. Porto Alegre. Vol. 41, no. 3 (2021), p. 205-211Citometria de fluxoCitocinasInflamaçãoNeoplasias renaisCytometric Bead Array (CBA)CytokinesIL-6InflammationRenal cancerIncreased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma developmentinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/otherinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSTEXT001134281.pdf.txt001134281.pdf.txtExtracted Texttext/plain26833http://www.lume.ufrgs.br/bitstream/10183/233453/2/001134281.pdf.txt5495c2c22c6a66136fe2b85118423628MD52ORIGINAL001134281.pdfTexto completo (inglês)application/pdf655309http://www.lume.ufrgs.br/bitstream/10183/233453/1/001134281.pdfaad3550456a8f2fd02d6a16263ce0933MD5110183/2334532024-01-06 04:36:26.909368oai:www.lume.ufrgs.br:10183/233453Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2024-01-06T06:36:26Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false |
dc.title.pt_BR.fl_str_mv |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
title |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
spellingShingle |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development Cechim, Giovana Citometria de fluxo Citocinas Inflamação Neoplasias renais Cytometric Bead Array (CBA) Cytokines IL-6 Inflammation Renal cancer |
title_short |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
title_full |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
title_fullStr |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
title_full_unstemmed |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
title_sort |
Increased systemic IL-6 levels point to inflammation as a determinant of renal cell carcinoma development |
author |
Cechim, Giovana |
author_facet |
Cechim, Giovana Ellwanger, Joel Henrique Kaminski, Valéria de Lima Berger, Milton Chies, Jose Artur Bogo |
author_role |
author |
author2 |
Ellwanger, Joel Henrique Kaminski, Valéria de Lima Berger, Milton Chies, Jose Artur Bogo |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Cechim, Giovana Ellwanger, Joel Henrique Kaminski, Valéria de Lima Berger, Milton Chies, Jose Artur Bogo |
dc.subject.por.fl_str_mv |
Citometria de fluxo Citocinas Inflamação Neoplasias renais |
topic |
Citometria de fluxo Citocinas Inflamação Neoplasias renais Cytometric Bead Array (CBA) Cytokines IL-6 Inflammation Renal cancer |
dc.subject.eng.fl_str_mv |
Cytometric Bead Array (CBA) Cytokines IL-6 Inflammation Renal cancer |
description |
Introduction: Renal cell carcinoma (RCC) is one of the most prevalent kidney tumors. Inflammation is believed to be a key factor in its progression and spread since inflammatory markers are generally associated with poor prognosis in RCC patients. Cytokines are cell communication molecules involved in both healthy and pathological processes, including tumor growth and progression. Recent findings suggest that cytokine level measurements could be used for cancer monitoring and prognosis. Methods: This study characterized and compared the levels of different cytokines associated with the classical Th1, Th2, and Th17 immune responses in plasma samples from RCC patients (n = 25) and healthy controls (n = 29). Cytokine levels (IL-2, IL-4, IL-6, IL-10, TNF-α, IFN-γ, and IL-17A) were evaluated by flow cytometry using a BD Cytometric Bead Array (CBA) kit. Results: No statistical differences in systemic IL-2, IL-4, IL-10, IL-17A, TNF, and INF-γ levels were observed between RCC patients and controls (p > 0.05). However, higher systemic IL-6 levels were observed in RCC patients (p = 0.0034). Conclusions: This study highlights the importance of assessing the impact of IL-6 on RCC pathogenesis and its potential role as a biomarker of disease progression. |
publishDate |
2021 |
dc.date.accessioned.fl_str_mv |
2021-12-29T04:27:19Z |
dc.date.issued.fl_str_mv |
2021 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/other |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10183/233453 |
dc.identifier.issn.pt_BR.fl_str_mv |
2357-9730 |
dc.identifier.nrb.pt_BR.fl_str_mv |
001134281 |
identifier_str_mv |
2357-9730 001134281 |
url |
http://hdl.handle.net/10183/233453 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.pt_BR.fl_str_mv |
Clinical and biomedical research. Porto Alegre. Vol. 41, no. 3 (2021), p. 205-211 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFRGS instname:Universidade Federal do Rio Grande do Sul (UFRGS) instacron:UFRGS |
instname_str |
Universidade Federal do Rio Grande do Sul (UFRGS) |
instacron_str |
UFRGS |
institution |
UFRGS |
reponame_str |
Repositório Institucional da UFRGS |
collection |
Repositório Institucional da UFRGS |
bitstream.url.fl_str_mv |
http://www.lume.ufrgs.br/bitstream/10183/233453/2/001134281.pdf.txt http://www.lume.ufrgs.br/bitstream/10183/233453/1/001134281.pdf |
bitstream.checksum.fl_str_mv |
5495c2c22c6a66136fe2b85118423628 aad3550456a8f2fd02d6a16263ce0933 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS) |
repository.mail.fl_str_mv |
|
_version_ |
1815447779042918400 |