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1.
Rev. bras. cancerol ; 61(1): 31-36, jan./mar. 2015.
Article in Portuguese | LILACS | ID: biblio-833775

ABSTRACT

Introdução: Atipia de células escamosas (ASC, atypical squamous cells) é a anormalidade epitelial mais frequente nos resultados de análises colpocitológicas e corresponde essencialmente a um grupo epidemiológico de incerteza. A razão entre as taxas de ASC e de lesões intraepitelias escamosas (SIL, squamous intraepithelial lesion) tem sido utilizada como uma ferramenta de controle de qualidade por muitos laboratórios de citopatologia. Objetivo: Avaliar a razão ASC/SIL anual, em um serviço de anatomia patológica de grande porte durante um período de dez anos, comparando com os valores preconizados pelo Colégio de Patologistas Americanos (CAP, College of American Pathologists); e averiguar sua utilidade como ferramenta de garantia da qualidade na interpretação citológica de ASC no laboratório de citopatologia. Método: Estudo transversal e retrospectivo (2002 a 2011) realizado com base nos registros de ASC e SIL do banco de dados de um serviço de anatomia patológica, em Joinville/SC. Todos os exames foram contabilizados, incluindo as citologias convencionais e as citologias em meio líquido. Foi estabelecida a razão ASC/SIL por ano e os resultados foram comparados com os índices preconizados pelo CAP. Resultados: Os índices encontrados da relação ASC/SIL apresentam-se dentro dos valores preconizados pelo CAP, com média de 1,467. Conclusão: A relação ASC/SIL oferece uma informação simples e eficaz para o laboratório de citopatologia sobre o uso de ASC como categoria diagnóstica, indicando a necessidade de adequações para elevação ou redução do índice sempre que necessário.


Subject(s)
Quality Control , Cell Biology , Papanicolaou Test , Atypical Squamous Cells of the Cervix , Squamous Intraepithelial Lesions of the Cervix
3.
J Virol ; 64(1): 264-77, 1990 Jan.
Article in English | MEDLINE | ID: mdl-2152815

ABSTRACT

A 600-base-pair (bp) enhancer region upstream from the major IE94 gene of simian cytomegalovirus (SCMV) produces very strong basal expression of associated gene products. This domain consists of multiple sets of interspersed repetitive elements, including 11 copies of a conserved 16-bp palindromic sequence with the consensus CCATTGACGTCAATGG. These series I repeats contain an 8-bp core TGACGTCA that resembles the cyclic AMP (cAMP) response element (CRE) of cellular genes. In transient chloramphenicol acetyltransferase assays in K562 human erythroleukemia cells, a set of deleted variants of the IE94 promoter all responded up to 15-fold to induction by cAMP. However, successive removal of most of the SCMV 16-bp motifs reduced basal expression over 20-fold. The cAMP stimulation was also manifested at the steady-state RNA level after SCMV infection of K562 cells and was detectable within 1.5 h after treatment of DNA-transfected cells. Addition of a single 30-bp oligonucleotide encompassing the 16-bp palindrome conveyed up to 10-fold cAMP responsiveness onto a heterologous weak promoter but had no effect on basal expression. In contrast, two or more adjacent copies produced 20- to 40-fold increases in basal expression and provided greater than 200-fold activation in the presence of cAMP. Similar effects were obtained when the oligonucleotides were placed in a downstream location relative to the reporter gene. Studies with mutant oligonucleotides revealed that both the core CRE and the flanking sequence portions of the 16-bp elements were essential for enhancer function. Both components were also important for maximum cAMP responsiveness. Band shift assays with fractionated nuclear extracts from Raji lymphocytes revealed multiple competable complexes with cellular DNA-binding factors that recognized the series I elements. Three distinct CREB-like factors were detected that required only the core 8-bp elements for binding. We conclude that the 16-bp series I repeats provide a major contribution to the constitutive enhancer properties of the IE94 promoter and also act as functional CREs. The cAMP response properties appear likely to play a key role in reactivation of the virus from a latent state in appropriately differentiating cell types.


Subject(s)
Cyclic AMP/physiology , Cytomegalovirus/genetics , Enhancer Elements, Genetic , Genes, Viral , Promoter Regions, Genetic , Animals , Base Sequence , Cell Line , Chlorocebus aethiops , Humans , Leukemia, Erythroblastic, Acute , Molecular Sequence Data , Oligonucleotide Probes , Repetitive Sequences, Nucleic Acid , Restriction Mapping , Signal Transduction , Transfection
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