Urban, traffic- related particles and lung tumors in urethane treated mice
Autor(a) principal: | |
---|---|
Data de Publicação: | 2011 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Clinics |
Texto Completo: | https://www.revistas.usp.br/clinics/article/view/19526 |
Resumo: | OBJECTIVE: The present study was designed to evaluate the effects of urban, traffic-related, fine particulate matter (PM2.5) on mice lung tumorigenesis under controlled exposure conditions. METHODS: Four groups of female Swiss mice were treated with intraperitonial injections of urethane and saline solution. Urethane was used to start the carcinogenesis process. The animals were housed in two chambers receiving filtered and polluted air. In the polluted air chamber, pollutant levels were low. After two months of exposure, the animals were euthanized and lung tumoral nodules were counted. RESULTS: Saline-treated animals showed no nodules. Urethane-treated animals showed 2.0+2.0 and 4.0+3.0 nodules respectively, in the filtered and non-filtered chambers (p = 0.02), thus showing experimental evidence of increased carcinogenic-induced lung cancer with increasing PM2.5 exposure. CONCLUSION: Our data support the concept that low levels of PM2.5 may increase the risk of developing lung tumors. |
id |
USP-19_44a8d4b70d342e3b3251129d95d39f34 |
---|---|
oai_identifier_str |
oai:revistas.usp.br:article/19526 |
network_acronym_str |
USP-19 |
network_name_str |
Clinics |
repository_id_str |
|
spelling |
Urban, traffic- related particles and lung tumors in urethane treated mice Air PollutantsParticulate MatterLung CancerLung NodulesUrethane OBJECTIVE: The present study was designed to evaluate the effects of urban, traffic-related, fine particulate matter (PM2.5) on mice lung tumorigenesis under controlled exposure conditions. METHODS: Four groups of female Swiss mice were treated with intraperitonial injections of urethane and saline solution. Urethane was used to start the carcinogenesis process. The animals were housed in two chambers receiving filtered and polluted air. In the polluted air chamber, pollutant levels were low. After two months of exposure, the animals were euthanized and lung tumoral nodules were counted. RESULTS: Saline-treated animals showed no nodules. Urethane-treated animals showed 2.0+2.0 and 4.0+3.0 nodules respectively, in the filtered and non-filtered chambers (p = 0.02), thus showing experimental evidence of increased carcinogenic-induced lung cancer with increasing PM2.5 exposure. CONCLUSION: Our data support the concept that low levels of PM2.5 may increase the risk of developing lung tumors. Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo2011-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/clinics/article/view/1952610.1590/S1807-59322011000600022Clinics; Vol. 66 No. 6 (2011); 1051-1054 Clinics; v. 66 n. 6 (2011); 1051-1054 Clinics; Vol. 66 Núm. 6 (2011); 1051-1054 1980-53221807-5932reponame:Clinicsinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/clinics/article/view/19526/21589Pereira, Fernanda Alves CangeranaLemos, MiriamMauad, ThaisAssunção, João Vicente deSaldiva, Paulo Hilário Nascimentoinfo:eu-repo/semantics/openAccess2012-05-23T16:46:45Zoai:revistas.usp.br:article/19526Revistahttps://www.revistas.usp.br/clinicsPUBhttps://www.revistas.usp.br/clinics/oai||clinics@hc.fm.usp.br1980-53221807-5932opendoar:2012-05-23T16:46:45Clinics - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Urban, traffic- related particles and lung tumors in urethane treated mice |
title |
Urban, traffic- related particles and lung tumors in urethane treated mice |
spellingShingle |
Urban, traffic- related particles and lung tumors in urethane treated mice Pereira, Fernanda Alves Cangerana Air Pollutants Particulate Matter Lung Cancer Lung Nodules Urethane |
title_short |
Urban, traffic- related particles and lung tumors in urethane treated mice |
title_full |
Urban, traffic- related particles and lung tumors in urethane treated mice |
title_fullStr |
Urban, traffic- related particles and lung tumors in urethane treated mice |
title_full_unstemmed |
Urban, traffic- related particles and lung tumors in urethane treated mice |
title_sort |
Urban, traffic- related particles and lung tumors in urethane treated mice |
author |
Pereira, Fernanda Alves Cangerana |
author_facet |
Pereira, Fernanda Alves Cangerana Lemos, Miriam Mauad, Thais Assunção, João Vicente de Saldiva, Paulo Hilário Nascimento |
author_role |
author |
author2 |
Lemos, Miriam Mauad, Thais Assunção, João Vicente de Saldiva, Paulo Hilário Nascimento |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Pereira, Fernanda Alves Cangerana Lemos, Miriam Mauad, Thais Assunção, João Vicente de Saldiva, Paulo Hilário Nascimento |
dc.subject.por.fl_str_mv |
Air Pollutants Particulate Matter Lung Cancer Lung Nodules Urethane |
topic |
Air Pollutants Particulate Matter Lung Cancer Lung Nodules Urethane |
description |
OBJECTIVE: The present study was designed to evaluate the effects of urban, traffic-related, fine particulate matter (PM2.5) on mice lung tumorigenesis under controlled exposure conditions. METHODS: Four groups of female Swiss mice were treated with intraperitonial injections of urethane and saline solution. Urethane was used to start the carcinogenesis process. The animals were housed in two chambers receiving filtered and polluted air. In the polluted air chamber, pollutant levels were low. After two months of exposure, the animals were euthanized and lung tumoral nodules were counted. RESULTS: Saline-treated animals showed no nodules. Urethane-treated animals showed 2.0+2.0 and 4.0+3.0 nodules respectively, in the filtered and non-filtered chambers (p = 0.02), thus showing experimental evidence of increased carcinogenic-induced lung cancer with increasing PM2.5 exposure. CONCLUSION: Our data support the concept that low levels of PM2.5 may increase the risk of developing lung tumors. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-01-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19526 10.1590/S1807-59322011000600022 |
url |
https://www.revistas.usp.br/clinics/article/view/19526 |
identifier_str_mv |
10.1590/S1807-59322011000600022 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/clinics/article/view/19526/21589 |
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.publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
publisher.none.fl_str_mv |
Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo |
dc.source.none.fl_str_mv |
Clinics; Vol. 66 No. 6 (2011); 1051-1054 Clinics; v. 66 n. 6 (2011); 1051-1054 Clinics; Vol. 66 Núm. 6 (2011); 1051-1054 1980-5322 1807-5932 reponame:Clinics instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Clinics |
collection |
Clinics |
repository.name.fl_str_mv |
Clinics - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
||clinics@hc.fm.usp.br |
_version_ |
1800222757728813056 |