Use este identificador para citar ou linkar para este item: http://sgc.anlis.gob.ar/handle/123456789/1937
Campo DCValoridioma
dc.contributor.authorBrocardo, Mariana G.es
dc.contributor.authorBianchini, Michelees
dc.contributor.authorRadrizzani, Martines
dc.contributor.authorReyes, Gloria B.es
dc.contributor.authorDugour, Andrea V.es
dc.contributor.authorTaminelli, Guillermo L.es
dc.contributor.authorGonzalez Solveyra, Césares
dc.contributor.authorSanta-Coloma, Tomás A.es
dc.date.accessioned2020-12-18T15:58:49Z-
dc.date.available2020-12-18T15:58:49Z-
dc.date.issued2001-06-22-
dc.identifier.issn0006-291X-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/1937-
dc.descriptionFil: Brocardo, Mariana G. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.descriptionFil: Bianchini, Michele. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.descriptionFil: Radrizzani, Martín. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica; Argentina.es
dc.descriptionFil: Reyes, Gloria B. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.descriptionFil: Dugour, Andrea V. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.descriptionFil: Taminelli, Guillermo L. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.descriptionFil: Gonzalez Solveyra, César. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.descriptionFil: Santa-Coloma, Tomás A. Instituto de Investigaciones Bioquímicas. Fundación Campomar; Argentina.es
dc.description.abstractThe adenomatous polyposis coli (APC) tumor suppressor protein is involved in the Wnt/wingless pathway, modulating beta-catenin activity. We report the development of a highly specific, chemically synthesized oligobody (oligonucleotide-based synthetic antibody), directed against the N-terminal region of APC. Using this reagent, we found that within 16 h of disrupting HT-29 cell-cell contacts by harvesting cells with trypsin/EDTA treatment and replating, APC was translocated from the cytoplasm to the nucleus. Five days after plating the cells, when the cells had returned to their normal confluent phenotype and cell-cell contacts were reestablished, APC returned to the cytoplasm. These results suggest that APC functions as part of a "sensor" system, and responds to the loss of cell-cell contacts by moving to the nucleus, and returning to the cytoplasm when the contacts are fully restored.es
dc.language.isoenes
dc.relation.ispartofBiochemical and biophysical research communicationses
dc.rightsClosed Access-
dc.subjectProteína de la Poliposis Adenomatosa del Colones
dc.subjectNeoplasias del Colones
dc.subjectProteínas del Citoesqueletoes
dc.subjectGenes APCes
dc.subjectUniones Intercelulareses
dc.subjectCélulas Tumorales Cultivadases
dc.titleAPC senses cell-cell contacts and moves to the nucleus upon their disruptiones
dc.typeArtículoes
dc.identifier.doi10.1006/bbrc.2001.5066-
anlis.essnrd1-
item.languageiso639-1en-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeArtículo-
item.cerifentitytypePublications-
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