The role of p300 in the tumor progression of oral squamous cell carcinoma. (26th August 2014)

• Record Type: Journal Article
• Authors: Cho, Young‐Ah; Hong, Ji‐Soo; Choe, Eun‐Jin; Yoon, Hye‐Jung; Hong, Seong‐Doo; Lee, Jae‐Il; Hong, Sam‐Pyo
• Is Part Of: Journal of oral pathology & medicine. Volume 44:Number 3(2015:Mar.)
• Page Start: 185
• Page End: 192
• Publication Date: 2014-08-26
• Subjects: oncogene -- oral squamous cell carcinoma -- p300 -- p53 -- tumor suppressor gene; Dentistry -- Periodicals; Teeth -- Diseases -- Periodicals; 617
• DOI: 10.1111/jop.12227
• Languages: English
• ISSNs: 0904-2512

Abstract

Abstract : Background: EP300 gene encoding p300 is a candidate tumor suppressor gene. This study investigated p300 expression and gene alteration in oral squamous cell carcinoma (OSCC) specimens to assess its role in OSCC development. Methods: Genomic DNA extracted from 13 human OSCC cell lines and 40 OSCC patient specimens was subjected to methylation‐specific PCR and exon sequencing. Immunohistochemical staining with primary antibodies against p300 and p53 was performed in 48 patients with OSCC. We analyzed the association between the data and clinicopathological factors of OSCC patients. Results: Methylation‐specific PCR revealed that the EP300 promoter region was not hypermethylated in OSCC. Only one cell line demonstrated a point mutation at exon 31. On immunohistochemical examination, patients with metastatic lymph nodes ( P = 0.009) and advanced clinical stage ( P = 0.046) tended to show increased expression of p300. There was no statistically significant relationship between p300 expression and p53 accumulation in OSCC tissue samples. Patient survival was not correlated with p300 expression. Conclusions: EP300 is not a tumor suppressor gene because there was neither epigenetic inactivation of the gene nor a mutation resulting in functional impairment. Based on p300 overexpression and its association with clinical factors in patients with OSCC, it is likely that p300 itself or one of its target genes plays a key role in the aggressive phenotypes of OSCC.