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口腔扁平苔藓中 COX-2 水平升高支持该病的自身免疫病因。

Increased levels of COX-2 in oral lichen planus supports an autoimmune cause of the disease.

机构信息

Department of Odontology, Umeå University, Umeå, Sweden.

出版信息

J Eur Acad Dermatol Venereol. 2012 Nov;26(11):1415-9. doi: 10.1111/j.1468-3083.2011.04306.x. Epub 2011 Oct 24.

DOI:10.1111/j.1468-3083.2011.04306.x
PMID:22017396
Abstract

BACKGROUND

Oral lichen planus (OLP) is a chronic inflammatory disease for which the pathogenesis is not fully understood. OLP has autoimmune features and auto immunity has been suggested as a potential cause, whereas WHO has classified OLP as a premalignant condition. Association between chronic inflammation and cancer is known and chronic inflammation is one of the characteristics of OLP. A protein connected to inflammation and suggested to be involved in cancer development is cyclooxygenase-2 (COX-2) which can be inhibited by microRNA-26b (miR-26b).

OBJECTIVE

The aim was to map levels of COX-2 and miR-26b in OLP lesions to see if there was any correlation between expression of COX-2 and its regulator miR-26b in OLP.

METHODS

In biopsies from 20 OLP patients and 20 age and gender-matched controls laser- micro dissection of epithelium was performed. Quantitative RT-PCR, immunohistochemistry and Western blot were used in the analysis.

RESULTS

Levels of COX-2 mRNA were significantly higher while levels of miR-26b were significantly lower in OLP lesions compared to controls. Using immunohistochemistry normal oral mucosa samples did not show any expression of COX-2 while OLP samples expressed the protein. No COX-2 protein was detectable with Western blot.

CONCLUSION

Increased expression of COX-2 and decreased expression of miR-26b in OLP suggests both to play a role in OLP. COX-2 has been connected to both malignant development and autoimmunity but as malignant development of OLP is quite rare we suggest that the increased levels of COX-2 seen here support an autoimmune cause of the disease.

摘要

背景

口腔扁平苔藓(OLP)是一种慢性炎症性疾病,其发病机制尚未完全阐明。OLP 具有自身免疫特征,自身免疫被认为是其潜在病因,而世界卫生组织(WHO)将 OLP 归类为癌前病变。慢性炎症与癌症之间存在关联,慢性炎症是 OLP 的特征之一。一种与炎症相关并被认为与癌症发展有关的蛋白是环氧化酶-2(COX-2),它可以被 microRNA-26b(miR-26b)抑制。

目的

本研究旨在检测 OLP 病变中 COX-2 和 miR-26b 的水平,以观察 COX-2 及其调控因子 miR-26b 在 OLP 中的表达是否存在相关性。

方法

对 20 例 OLP 患者和 20 例年龄和性别匹配的对照者的活检组织进行激光微切割,采用定量 RT-PCR、免疫组织化学和 Western blot 进行分析。

结果

与对照组相比,OLP 病变中 COX-2 mRNA 水平显著升高,而 miR-26b 水平显著降低。免疫组织化学显示,正常口腔黏膜样本中无 COX-2 表达,而 OLP 样本中表达该蛋白。Western blot 未检测到 COX-2 蛋白。

结论

OLP 中 COX-2 表达增加和 miR-26b 表达降低提示两者均在 OLP 中发挥作用。COX-2 与恶性发展和自身免疫均有关,但由于 OLP 的恶性发展相当罕见,我们认为此处观察到的 COX-2 水平升高支持该疾病的自身免疫病因。

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