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dc.contributor.author
Pagura, Lucas  
dc.contributor.author
Cáceres, Juan Manuel  
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Cardinale, Albertina  
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Scharovsky, Olga Graciela  
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Di Masso, Ricardo Jose  
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Zacarías Fluck, Mariano Federico  
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Rico, María José  
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Rozados, Viviana Rosa  
dc.date.available
2023-01-27T10:44:49Z  
dc.date.issued
2014-05  
dc.identifier.citation
Pagura, Lucas; Cáceres, Juan Manuel; Cardinale, Albertina; Scharovsky, Olga Graciela; Di Masso, Ricardo Jose; et al.; A mammary adenocarcinoma murine model suitable for the study of cancer immunoediting; BioMed Central; Journal Of Biomedical Science; 21; 5-2014; 21-52  
dc.identifier.issn
1021-7770  
dc.identifier.uri
http://hdl.handle.net/11336/185853  
dc.description.abstract
Background: Cancer immunoediting is a dynamic process composed of three phases: elimination (EL), equilibrium (EQ) and escape (ES) that encompasses the potential host-protective and tumor-sculpting functions of the immune system throughout tumor development. Animal models are useful tools for studying diseases such as cancer. The present study was designed to characterize the interaction between mammary adenocarcinoma M-406 and CBi, CBi- and CBi/L inbred mice lines. Results: The mammary adenocarcinoma M-406 developed spontaneously in a CBi mouse. CBi/L and CBi- mice were artificially selected for body conformation from CBi. When CBi mice are s.c. challenged with M-406, tumor growths exponentially in 100% of animals, while in CBi- the tumor growths briefly and then begins a rejection process in 100% of the animals. In CBi/L the growth of the tumor shows the three phases: 51.6% in ES, 18.5% in EQ and 29.8% in EL. Conclusions: The results obtained support the conclusion that the system M-406 plus the inbred mouse lines CBi, CBi - and CBi/L, is a good murine model to study the process of tumor immunoediting.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
BioMed Central  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
CANCER IMMUNOEDITING  
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MAMMARY ADENOCARCINOMA  
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MATHEMATICAL MODEL  
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MURINE MODELS  
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Otras Ciencias Biológicas  
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Ciencias Biológicas  
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CIENCIAS NATURALES Y EXACTAS  
dc.title
A mammary adenocarcinoma murine model suitable for the study of cancer immunoediting  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2023-01-26T17:30:10Z  
dc.journal.volume
21  
dc.journal.pagination
21-52  
dc.journal.pais
Reino Unido  
dc.journal.ciudad
Londres  
dc.description.fil
Fil: Pagura, Lucas. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Rosario. Instituto de Biología Molecular y Celular de Rosario. Universidad Nacional de Rosario. Facultad de Ciencias Bioquímicas y Farmacéuticas. Instituto de Biología Molecular y Celular de Rosario; Argentina  
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Fil: Cáceres, Juan Manuel. Universidad Nacional de Rosario. Facultad de Ciencias Medicas. Instituto de Genetica Experimental; Argentina  
dc.description.fil
Fil: Cardinale, Albertina. Universidad Nacional de Rosario. Facultad de Ciencias Medicas. Instituto de Genetica Experimental; Argentina  
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Fil: Scharovsky, Olga Graciela. Universidad Nacional de Rosario. Facultad de Ciencias Medicas. Instituto de Genetica Experimental; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
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Fil: Di Masso, Ricardo Jose. Universidad Nacional de Rosario. Facultad de Ciencias Medicas. Instituto de Genetica Experimental; Argentina  
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Fil: Zacarías Fluck, Mariano Federico. Vall d’Hebron Institute of Oncology; España  
dc.description.fil
Fil: Rico, María José. Universidad Nacional de Rosario. Facultad de Ciencias Medicas. Instituto de Genetica Experimental; Argentina  
dc.description.fil
Fil: Rozados, Viviana Rosa. Universidad Nacional de Rosario. Facultad de Ciencias Medicas. Instituto de Genetica Experimental; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina  
dc.journal.title
Journal Of Biomedical Science  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.jbiomedsci.com/content/21/1/52  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1186/1423-0127-21-52