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dc.contributor.authorRoa, I.
dc.contributor.authorCantín, M.
dc.contributor.authorMuñoz, M.
dc.contributor.authorRosas, C.
dc.contributor.authorLemus, D.
dc.date.accessioned2025-10-31T18:42:42Z
dc.date.available2025-10-31T18:42:42Z
dc.date.issued2016
dc.identifier.urihttps://hdl.handle.net/20.500.12805/5990
dc.description.abstractAngiogenesis and metastasis are critical events on the tumor invasion process. Their close association is related as a good target in antitumor therapy. The aimwas to analyze lung metastasis pattern and angiogenesis following application of microencapsulated Celecoxib with poli(lactic-co-glycolic) acid in mice.An experimental tumor model was assessed, induced by TA3-MTX-R cells, in 18 mice, separated in 3 groups of 6 animals and treated with 2 intramuscular Celecoxib presentations (Group Control; Group Cx 1000 ppm and Group Cx 1000 ppm+PLGA). Mice were sacrificed and histologically processed to stain slides with H&E andArteta Trichromic. The study revealed that the lung showed a significant heterogeneity, and a perivascular metastasis pattern; moreover, Celecoxib associated to poli(lactic-co-glycolic) acid reduces tumor invasion and pulmonary angiogenesis. The results are similar to partial previous descriptions and are comparable to other tumor lines, concluding that Celecoxib/poli(lactic-co-glycolic) acid is a potential candidate in antitumor therapy.en_US
dc.formatapplication/pdf
dc.language.isospa
dc.publisherUniversidad de la Frontera
dc.relation.ispartofurn:issn:0717-9502
dc.rightshttps://purl.org/coar/access_right/c_abf2
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectSDG 3en_US
dc.subjectImpact of Anti-Inflammatory Drugs on Cancer Progressionen_US
dc.subjectCyclooxygenase 2 Role in Cancer Progressionen_US
dc.titleCelecoxib/PLGA Suprime Angiogénesis y Metástasis Pulmonar de un Cáncer Mamario Murino Experimentales_PE
dc.title.alternativeCelecoxib/PLGA suppresses angiogenesis and lung metastasis of murine experimental breast canceren_US
dc.typehttps://purl.org/coar/resource_type/c_2df8fbb1
dc.identifier.doihttps://doi.org/10.4067/S0717-95022016000100048
dc.subject.ocdehttps://purl.org/pe-repo/ocde/ford#3.01.00
dc.type.otherResearch article
dc.identifier.journalInternational Journal of Morphology
dc.type.versionhttps://purl.org/coar/version/c_970fb48d4fbd8a85


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