Coexpression of p53 protein and MDR functional phenotype in leukemias: the predominant association in chronic myeloid leukemia

dc.contributor.authorCavalcanti Junior, Geraldo Barroso
dc.contributor.authorVasconcelos, Flavia da Cunha
dc.contributor.authorFaria, Giselle Pinto de
dc.contributor.authorScheiner, Marcos Antônio Maurício
dc.contributor.authorDobbin, Jane de Almeida
dc.contributor.authorKlumb, Claudete Esteves
dc.contributor.authorMaia, Raquel C.
dc.contributor.authorIDhttps://orcid.org/0000-0001-9227-4145pt_BR
dc.date.accessioned2023-01-20T20:11:16Z
dc.date.available2023-01-20T20:11:16Z
dc.date.issued2004
dc.description.resumoBackground: One of the best characterized resistance mechanisms of leukemias is multidrug resistance (MDR) mediated by P-glycoprotein (Pgp) and multidrug-resistant related protein (MRP). In addition to Pgp and MRP, p53 mutation or inactivation might play a relevant role in therapeutic failure. Some studies have demonstrated that Pgp and MRP may be activated in association with overexpression of mutant or inactivated p53 protein. The aim of this study was to investigate the association between p53 expression and MDR functional phenotype analyzed by flow cytometry (FCM). Methods: Rhodamine-123 assay analyzed by FCM was used to detect the MDR phenotype that was positive in 18 out of 41 (43.9%) cases of chronic myeloid leukemia (CML), 16 out of 28 (57.1%) chronic lymphoid leukemia (CLL) cases, 11 out of 28 (39.3%) acute myeloid leukemia (AML) cases, and four out of 22 (18.2%) acute lymphoid leukemia (ALL) cases. Results: Variable levels of p53 expression were observed in leukemic cells: 12 out of 41 (29.2%) in CML, nine out of 28 (32.1%) in CLL, 15 out of 28 (53.6%) in AML, and eight out of 22 (36.4%) in ALL samples. Conclusions: In our study, no significant association between p53 expression and MDR functional phenotype was observed in ALL, CLL, and AML. On the other hand, a significant association (P 0.0003) of the coexpression was observed in CML. The p53 overexpression was more frequently seen in the accelerated phase and the blastic phase of this disease. Our results suggest that an MDR functional phenotype could be associated with p53 mutation in the advanced stage of leukemias.pt_BR
dc.identifier.citationCAVALCANTI JÚNIOR, Geraldo Barroso et al. Coexpression of p53 protein and MDR functional phenotype in leukemias: the predominant association in chronic myeloid leukemia. Cytometry Part B: Clinical Cytometry: The Journal of the International Society for Analytical Cytology, v. 61, n. 1, p. 1-8, 2004. Disponível em: https://onlinelibrary.wiley.com/doi/full/10.1002/cyto.b.20013. Acesso em: 20 jan. 2023.pt_BR
dc.identifier.issn1552-4957
dc.identifier.urihttps://repositorio.ufrn.br/handle/123456789/51006
dc.languageenpt_BR
dc.publisherWileypt_BR
dc.rightsAttribution-ShareAlike 3.0 Brazil*
dc.rights.urihttp://creativecommons.org/licenses/by-sa/3.0/br/*
dc.subjectChronic myeloid leukemiapt_BR
dc.subjectAcute myeloid leukemiapt_BR
dc.subjectMultidrug resistancept_BR
dc.subjectP53 proteinpt_BR
dc.titleCoexpression of p53 protein and MDR functional phenotype in leukemias: the predominant association in chronic myeloid leukemiapt_BR
dc.typearticlept_BR

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