School of Dentistry, Mae Fah Luang University, Chiangrai, Thailand.
Department of Oral Pathology, Faculty of Dentistry, Chulalongkorn University, Bangkok, Thailand.
Int Dent J. 2024 Aug;74(4):769-776. doi: 10.1016/j.identj.2024.01.011. Epub 2024 Feb 6.
Oral carcinogenesis is complex and influenced by both genetic and epigenetic changes. Altered histone modification is the epigenetic event that plays a role in cancer development and progression. Distinct modification patterns of histones have been shown to affect patient prognosis in selected cancers. This study aimed to evaluate the profiles of histone H3 modification in oral epithelial dysplasia (OED) and oral squamous cell carcinoma (OSCC) in association with the clinical-pathologic characteristics.
One hundred patients were divided into 4 groups: low-grade OED, high-grade OED, OSCC, and normal oral mucosa (NOM). The levels of 3 types of histone modification-the H3K18ac, H3K9me3, and H3K9ac-were analysed immunohistochemically. Their expression profiles were compared and correlated with prognostically relevant clinical and pathologic features.
The H3K18ac and H3K9me3 were upregulated in OSCC, compared with OED and NOM. In contrast, the H3K9ac was downregulated in low-grade OED but increased in high-grade OED and OSCC. The hyperacetylations of H3K18 and H3K9 significantly correlated with advanced cancer depth of invasion and high T stage, respectively.
Histone H3 acetylation and methylation at lysine residues are differentially involved in the multistep oral carcinogenesis and impact aggressive cancer phenotypes. The effect of H3K9ac appears early in OED development, whilst the increased H3K18ac and H3K9me3 may be vital in the emergence of OSCC.
口腔癌发生机制复杂,受遗传和表观遗传改变的影响。组蛋白修饰的改变是癌症发生和发展中起作用的表观遗传事件。已有研究表明,在某些癌症中,组蛋白的不同修饰模式会影响患者的预后。本研究旨在评估口腔上皮异型增生(OED)和口腔鳞状细胞癌(OSCC)中组蛋白 H3 修饰谱与临床病理特征的相关性。
100 名患者被分为 4 组:低级别 OED、高级别 OED、OSCC 和正常口腔黏膜(NOM)。采用免疫组织化学方法分析 3 种组蛋白修饰类型(H3K18ac、H3K9me3 和 H3K9ac)的水平。比较它们的表达谱,并与预后相关的临床和病理特征相关联。
与 OED 和 NOM 相比,OSCC 中 H3K18ac 和 H3K9me3 上调。相反,低级别 OED 中 H3K9ac 下调,而高级别 OED 和 OSCC 中 H3K9ac 上调。H3K18 和 H3K9 的乙酰化与癌症浸润深度的进展和 T 分期的升高显著相关。
赖氨酸残基上的组蛋白 H3 乙酰化和甲基化在口腔多步骤癌变中差异参与,并影响侵袭性癌症表型。H3K9ac 的作用在 OED 发展早期出现,而 H3K18ac 和 H3K9me3 的增加可能在 OSCC 的出现中至关重要。