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Impact of WWOX alterations on p73, ΔNp73, p53, cell proliferation and DNA ploidy in salivary gland neoplasms
Author(s) -
Gomes CC,
Diniz MG,
Oliveira CS,
Tavassoli M,
Odell EW,
Gomez RS,
De Marco L
Publication year - 2011
Publication title -
oral diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.953
H-Index - 87
eISSN - 1601-0825
pISSN - 1354-523X
DOI - 10.1111/j.1601-0825.2011.01802.x
Subject(s) - wwox , cancer research , immunohistochemistry , biology , exon , dna methylation , methylation , transcription (linguistics) , gene , gene expression , suppressor , immunology , genetics , linguistics , philosophy
Oral Diseases17 , 564–571 Objective: WWOX gene is altered in a variety of neoplasms. Wwox is pro‐apoptotic through interaction with p73 and may be involved in chromosomal stability by interaction with p73 and p53. The aims of this study were to characterize WWOX transcription, methylation status and immunoexpression in salivary neoplasms and to determine whether these were associated with p73, p53, cell proliferation and DNA ploidy. Materials and Methods: Seven malignant and 21 benign fresh salivary neoplasms were included. WWOX expression was determined by RT‐PCR and sequencing of transcripts, quantitative PCR and immunohistochemistry. Methylation‐specific PCR was used to assess the methylation of its first exon. For p73, ΔNp73, p53 and ki67 immunohistochemistry and ploidy analysis, 29 malignant samples from archives were included. Results: No consistent pattern of WWOX exon 1 methylation was found, but aberrant and novel transcripts were observed in 17/28 neoplasms; 55% of tumours showed reduced WWOX RNA. WWOX RNA levels were associated with p53 immunopositivity. Immunohistochemical Wwox expression did not correlate with methylation status, p53 or p73 expression or proliferation. p73, proliferation and DNA ploidy were associated with malignant phenotype. Conclusion: Aberrant WWOX transcription and decreased expression are frequent in salivary neoplasms and WWOX transcription is associated with p53 staining.