Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/33065
Title: Claudin-7 down-regulation is an important feature in oral squamous cell carcinoma
Authors: Lourenco, Silvia Vanessa
Coutinho-Camillo, Claudia Malheiros
Cavicchioli Buim, Marcilei Elisa
Carvalho, Ana Carolina de [UNIFESP]
Lessa, Roberta Cardim
Pereira, Claudia Maria
Vettore, Andre Luiz [UNIFESP]
Carvalho, Andre Lopes
Fregnani, Jose Humberto
Kowalski, Luiz Paulo
Soares, Fernando Augusto
Universidade de São Paulo (USP)
Hosp AC Camargo Fund Antonio Prudente
Universidade Federal de São Paulo (UNIFESP)
Ludwig Inst Canc Res
Hosp Canc Barretos
Keywords: claudin-7
oral cancer
tight junction
tissue microarray
Issue Date: 1-Nov-2010
Publisher: Wiley-Blackwell
Citation: Histopathology. Malden: Wiley-Blackwell Publishing, Inc, v. 57, n. 5, p. 689-698, 2010.
Abstract: Aims:Claudins, a large family of essential tight junction (TJ) proteins, are abnormally regulated in human carcinomas, especially claudin-7. the aim of this study was to investigate claudin-7 expression and alterations in oral squamous cell carcinoma (OSCC).Methods and results:Expression of claudin-7 was analysed in 132 cases of OSCC organized in a tissue microarray. Claudin-7 mRNA transcript was evaluated using real-time polymerase chain reaction and the methylation status of the promoter was also assessed. Claudin-7 was negative in 58.3% of the cases. Loss of claudin-7 protein expression was associated with recurrence (P = 0.019), tumour size (P = 0.014), clinical stage of OSCC (P = 0.055) and disease-free survival (P = 0.015). Down-regulation of the claudin-7 mRNA transcripts was observed in 78% of the cases, in accordance with immunoexpression. Analysis of the methylation status of the promoter region of claudin-7 revealed that treatment of O28 cells (that did not express claudin-7 mRNA transcripts) with 5-Aza-2'-Deoxycytidine (5-Aza-dC) led to the re-expression of claudin-7 mRNA transcript.Conclusion:Loss of claudin-7 expression is associated with important subcellular processes in OSCC with impact on clinical parameters.
URI: http://repositorio.unifesp.br/handle/11600/33065
ISSN: 0309-0167
Other Identifiers: http://dx.doi.org/10.1111/j.1365-2559.2010.03685.x
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