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dc.creatorLIMA, Eleonidas Moura-
dc.creatorRISSINO, Jorge Dores-
dc.creatorHARADA, Maria Lúcia-
dc.creatorASSUMPÇÃO, Paulo Pimentel de-
dc.creatorDEMACHKI, Samia-
dc.creatorCASARTELLI, Cacilda-
dc.creatorSMITH, Marília de Arruda Cardoso-
dc.creatorRODRÍGUEZ BURBANO, Rommel Mario-
dc.creatorGUIMARÃES, Adriana Costa-
dc.date.accessioned2011-06-20T15:10:44Z-
dc.date.available2011-06-20T15:10:44Z-
dc.date.issued2004-12-
dc.identifier.citationLIMA, E.M. et al. Conventional cytogenetic characterization of a new cell line, ACP01, established from a primary human gastric tumor. Brazilian Journal of Medical and Biological Research, Ribeirão Preto, v. 37, n. 12, p. 1831-1838, dez. 2004. Disponível em: <http://www.scielo.br/pdf/bjmbr/v37n12/5389.pdf>. Acesso em: 20 jun. 2011. <http://dx.doi.org/10.1590/S0100-879X2004001200008>.pt_BR
dc.identifier.issn1414-431X-
dc.identifier.urihttp://www.repositorio.ufpa.br:8080/jspui/handle/2011/2274-
dc.description.abstractGastric cancer is the second most frequent type of neoplasia and also the second most important cause of death in the world. Virtually all the established cell lines of gastric neoplasia were developed in Asian countries, and western countries have contributed very little to this area. In the present study we describe the establishment of the cell line ACP01 and characterize it cytogenetically by means of in vitro immortalization. Cells were transformed from an intestinal-type gastric adenocarcinoma (T4N2M0) originating from a 48-year-old male patient.This is the first gastric denocarcinoma cell line established in Brazil. The most powerful application of the cell line ACP01 is in the assessment of cytotoxicity. Solid tumor cell lines from different origins have been treated with several conventional and investigational anticancer drugs. The ACP01 cell line is triploid, grows as a single, non-organized layer, similar to fibroblasts, with focus formation,heterogeneous division, and a cell cycle of approximately 40 h. Chromosome 8 trisomy, present in 60% of the cells, was the most frequent cytogenetic alteration. These data lead us to propose a multifactorial triggering of gastric cancer which evolves over multiple stages involving progressive genetic changes and clonal expansion.pt_BR
dc.description.provenanceSubmitted by Albirene Sousa (albirene@ufpa.br) on 2011-06-20T15:10:44Z No. of bitstreams: 2 Lima_Gumarães.pdf: 624457 bytes, checksum: 0bdd2cc0fc3b1ce0b1824e6638de3968 (MD5) license_rdf: 23422 bytes, checksum: b145eda3d84bdc4f56b389c0ab98d368 (MD5)en
dc.description.provenanceMade available in DSpace on 2011-06-20T15:10:44Z (GMT). No. of bitstreams: 2 Lima_Gumarães.pdf: 624457 bytes, checksum: 0bdd2cc0fc3b1ce0b1824e6638de3968 (MD5) license_rdf: 23422 bytes, checksum: b145eda3d84bdc4f56b389c0ab98d368 (MD5) Previous issue date: 2004en
dc.language.isoengpt_BR
dc.rightsAcesso Abertopt_BR
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subjectEstômago-
dc.subjectAdenocarcinoma gástrico humano-
dc.subjectNeoplasias gástricas-
dc.titleConventional cytogenetic characterization of a new cell line, ACP01, established from a primary human gastric tumorpt_BR
dc.typeArtigo de Periódicopt_BR
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