Logotipo do repositório
 

Publicação:
Immunocytochemistry associated with oral exfoliative cytology: Methodological analysis

dc.contributor.authorda Silva, Alessandra Dutra
dc.contributor.authorLima, Celina Faig [UNESP]
dc.contributor.authorMaraschin, Bruna Jalfim
dc.contributor.authorLaureano, Natália Koerich
dc.contributor.authorDaroit, Natália Batista
dc.contributor.authorBrochier, Fernanda
dc.contributor.authorSant'Ana Filho, Manoel
dc.contributor.authorVisioli, Fernanda
dc.contributor.authorRados, Pantelis Varvaki
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2022-04-28T19:01:02Z
dc.date.available2022-04-28T19:01:02Z
dc.date.issued2015-01-01
dc.description.abstractObjective: To evaluate different immunocytochemical protocol variations to find the most effective protocol for the analysis of involucrin, epidermal growth factor receptor (EGFR), and E-cadherin antibodies. Exfoliative cytology is a noninvasive method used to monitor and screen for early changes in the oral mucosa of patients exposed to carcinogens such as tobacco and alcohol. It has been postulated that its association with immunocytochemistry may improve the effectiveness of the screening process. Study Design: Four graduate students from Porto Alegre in southern Brazil had oral smears collected from the border of the tongue using a cytobrush. The following variables were analyzed: cell membrane permeability, antigen retrieval method (microwave oven or water bath), antibody incubation time (overnight or 1 hour), detection system used (Envision or LSAB), and chromogen incubation time (10 seconds or 5 minutes). Results: Best results were obtained with the following combinations: (1) for involucrin: water bath, 1-hour incubation for primary antibody, Envision, and chromogen incubation for 10 seconds; (2) for EGFR: microwave, overnight incubation, LSAB, and chromogen incubation for 5 minutes; and (3) for E-cadherin: water bath, overnight incubation, Envision, and chromogen incubation for 5 minutes. Conclusion: Our findings suggest that each antibody requires a specific immunocytochemical protocol to guarantee optimal results with oral smears.en
dc.description.affiliationDepartment of Oral Pathology, School of Dentistry, Universidade Federal do Rio Grande do Sul
dc.description.affiliationDepartment of Biosciences and Oral Diagnosis, School of Dentistry, Institute of Science and Technology, Universidade Estadual Paulista
dc.description.affiliationUnespDepartment of Biosciences and Oral Diagnosis, School of Dentistry, Institute of Science and Technology, Universidade Estadual Paulista
dc.format.extent134-138
dc.identifier.citationAnalytical and Quantitative Cytology and Histology, v. 37, n. 2, p. 134-138, 2015.
dc.identifier.issn0884-6812
dc.identifier.scopus2-s2.0-84928806970
dc.identifier.urihttp://hdl.handle.net/11449/220356
dc.language.isoeng
dc.relation.ispartofAnalytical and Quantitative Cytology and Histology
dc.sourceScopus
dc.subjectE-cadherin antibodies
dc.subjectEpidermal growth factor receptor (EGFR)
dc.subjectExfoliative cytology
dc.subjectImmunocytochemistry
dc.subjectInvolucrin
dc.subjectOral cytopathology
dc.subjectOral exfoliative cytology
dc.subjectOral smears
dc.titleImmunocytochemistry associated with oral exfoliative cytology: Methodological analysisen
dc.typeArtigo
dspace.entity.typePublication

Arquivos

Coleções