Histone H3K9 Methylation Is Differentially Modified in Odontogenic Cyst and Tumors.

Q1 Dentistry
Ekarat Phattarataratip, Aroonwan Lam-Ubol
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引用次数: 0

Abstract

Objectives:  Histone modification in odontogenic lesions is mostly unexplored. Trimethylation of histone H3 at lysine residue 9 (H3K9Me3) has been studied in various pathologic conditions and showed biological significance promising for future therapeutic application. This study aimed to investigate the level and clinical relevance of the H3K9Me3 histone modification in odontogenic cysts and tumors.

Materials and methods:  A total of 105 cases of odontogenic lesions, comprising 30 odontogenic keratocysts (OKCs), 30 adenomatoid odontogenic tumors (AOTs), 30 ameloblastomas, and 15 dental follicles, were included in the study. The paraffin-embedded tissues were immunohistochemically stained for H3K9Me3. Both the intensity and the distribution of staining were evaluated and calculated as H-score. The correlation between the H3K9Me3 expression and the clinical characteristics of each lesion was evaluated.

Statistical analysis:  The Kruskal-Wallis test followed by Bonferroni's correction was performed to assess the differences in H-score among groups. In addition, Pearson's chi-squared test or Mann-Whitney U test was used to analyze potential factors that could affect protein expression.

Results:  The reduced enamel epithelium of the dental follicle showed uniformly strong H3K9Me3 expression. All odontogenic cysts and tumors examined demonstrated a significantly reduced H3K9Me3 level compared with dental follicles. The AOT showed the lowest H3K9Me3 level, followed by OKC and ameloblastoma. Its immunoreactivity was mainly localized in the basal and parabasal cells of OKC and the whorled/duct-like structures of AOT. Ameloblastoma exhibited marked variation in the H3K9Me3 level among cases. Notably, the upregulated H3K9Me3 was related to multilocularity of OKC and ameloblastoma.

Conclusions:  Histone H3K9 methylation is differentially expressed in odontogenic cysts and tumors. This epigenetic modification may contribute to the pathogenesis and aggressive behavior of odontogenic lesions.

组织蛋白 H3K9 甲基化在牙源性囊肿和肿瘤中的不同改变
目的:牙源性病变中的组蛋白修饰大多尚未得到研究。组蛋白 H3 在赖氨酸残基 9 处的三甲基化(H3K9Me3)已在多种病理情况下进行了研究,并显示出有望在未来应用于治疗的生物学意义。本研究旨在探讨H3K9Me3组蛋白修饰在牙源性囊肿和肿瘤中的水平和临床意义:本研究共纳入 105 例牙源性病变,包括 30 例牙源性角化囊肿(OKCs)、30 例腺样牙源性肿瘤(AOTs)、30 例牙釉质母细胞瘤和 15 例牙囊肿。对石蜡包埋的组织进行了 H3K9Me3 免疫组化染色。对染色的强度和分布进行评估,并以H-score计算。评估H3K9Me3表达与各病变临床特征之间的相关性:采用 Kruskal-Wallis 检验和 Bonferroni 校正来评估各组间 H-score 的差异。此外,还使用皮尔逊卡方检验或曼-惠特尼U检验来分析可能影响蛋白质表达的潜在因素:结果:牙泡中的釉质上皮细胞的H3K9Me3表达量一致较高。与牙囊相比,所有受检的牙源性囊肿和肿瘤的H3K9Me3水平都显著降低。AOT的H3K9Me3水平最低,其次是OKC和釉母细胞瘤。其免疫反应主要定位于 OKC 的基底细胞和副基底细胞以及 AOT 的轮状/导管样结构。釉母细胞瘤的 H3K9Me3 水平在不同病例中表现出明显的差异。值得注意的是,H3K9Me3的上调与OKC和母细胞瘤的多形性有关:结论:组蛋白 H3K9 甲基化在牙源性囊肿和肿瘤中有不同程度的表达。结论:组蛋白 H3K9 甲基化在牙源性囊肿和肿瘤中有不同程度的表达,这种表观遗传修饰可能有助于牙源性病变的发病机制和侵袭行为。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Journal of Dentistry
European Journal of Dentistry Dentistry-Dentistry (all)
CiteScore
5.10
自引率
0.00%
发文量
161
期刊介绍: The European Journal of Dentistry is the official journal of the Dental Investigations Society, based in Turkey. It is a double-blinded peer-reviewed, Open Access, multi-disciplinary international journal addressing various aspects of dentistry. The journal''s board consists of eminent investigators in dentistry from across the globe and presents an ideal international composition. The journal encourages its authors to submit original investigations, reviews, and reports addressing various divisions of dentistry including oral pathology, prosthodontics, endodontics, orthodontics etc. It is available both online and in print.
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