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HuR的细胞质表达可能是一种有价值的诊断工具,用于确定口腔疣状边缘性病变的恶性转化潜能。

Cytoplasmic expression of HuR may be a valuable diagnostic tool for determining the potential for malignant transformation of oral verrucous borderline lesions.

作者信息

Habiba Umma, Kitamura Tetsuya, Yanagawa-Matsuda Aya, Hida Kyoko, Higashino Fumihiro, Ohiro Yoichi, Totsuka Yasunori, Shindoh Masanobu

机构信息

Department of Oral Pathology and Biology, Hokkaido University Graduate School of Dental Medicine, Kita-ku, Sapporo 060-8586, Japan.

Department of Vascular Biology, Hokkaido University Graduate School of Dental Medicine, Kita-ku, Sapporo 060-8586, Japan.

出版信息

Oncol Rep. 2014 Apr;31(4):1547-54. doi: 10.3892/or.2014.3017. Epub 2014 Feb 10.

DOI:10.3892/or.2014.3017
PMID:24534848
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3975986/
Abstract

Oral verrucous carcinoma (OVC) is a low grade variant of oral squamous cell carcinoma, and oral verrucous hyperplasia (OVH) is a benign lesion without malignant features. However, pathologists are sometimes presented with borderline lesions and are indecisive as to diagnose them as benign or malignant. Thus, these lesions are tentatively termed oral verrucous lesions (OVLs). HuR is an ARE mRNA-binding protein, normally localized in the nucleus but cytoplasmic exportation is frequently observed in cancer cells. The present study aimed to elucidate whether expression of the HuR protein facilitates the diagnosis of true malignant lesions. Clinicopathological features were evaluated, and immunohistochemical analysis for p53, Ki67 and HuR proteins was performed in 48 cases of OVH, OVC and OVL, and the outcomes were correlated using appropriate statistical analysis. The association of these three proteins in relation to malignant transformation was analyzed after a 3-year follow-up of 25 OVL cases. The basal characteristics (age, gender and location) of all cases had no significant association with the types of lesions. Gingiva (39.4%) was the common site for all lesions. Distribution of the examined proteins had a significant association with the lesions. As compared with the OVLs, the number of immunostained-positive cells was significantly higher in the OVCs and lower in the OVH cases. During follow-up, 24% of the OVLs underwent malignant transformation for which high HuR expression and a diffuse staining pattern in the epithelium were observed. Taken together, the high degree of HuR expression with diffuse staining pattern in the epithelium may be an effective diagnostic tool that determines the potential of OVLs for malignant transformation.

摘要

口腔疣状癌(OVC)是口腔鳞状细胞癌的一种低级别变体,而口腔疣状增生(OVH)是一种无恶性特征的良性病变。然而,病理学家有时会遇到临界病变,难以确定将其诊断为良性还是恶性。因此,这些病变被暂称为口腔疣状病变(OVL)。HuR是一种ARE mRNA结合蛋白,通常定位于细胞核,但在癌细胞中经常观察到其向细胞质的输出。本研究旨在阐明HuR蛋白的表达是否有助于诊断真正的恶性病变。评估了临床病理特征,并对48例OVH、OVC和OVL病例进行了p53、Ki67和HuR蛋白的免疫组织化学分析,并使用适当的统计分析对结果进行了相关性分析。对25例OVL病例进行3年随访后,分析了这三种蛋白与恶性转化的关系。所有病例的基本特征(年龄、性别和部位)与病变类型无显著相关性。牙龈(39.4%)是所有病变的常见部位。所检测蛋白的分布与病变有显著相关性。与OVL相比,OVC中免疫染色阳性细胞数量显著更高,而OVH病例中则更低。随访期间,24%的OVL发生了恶性转化,观察到HuR高表达和上皮弥漫性染色模式。综上所述,上皮中HuR高表达伴弥漫性染色模式可能是一种有效的诊断工具,可用于确定OVL的恶性转化潜能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/07854ff09d67/OR-31-04-1547-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/4211e0897fc1/OR-31-04-1547-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/12cbb6902434/OR-31-04-1547-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/514d35d5bdac/OR-31-04-1547-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/dd9c4ee7a58e/OR-31-04-1547-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/b3703dc6086a/OR-31-04-1547-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/07854ff09d67/OR-31-04-1547-g05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/4211e0897fc1/OR-31-04-1547-g00.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/12cbb6902434/OR-31-04-1547-g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/514d35d5bdac/OR-31-04-1547-g02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/dd9c4ee7a58e/OR-31-04-1547-g03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/b3703dc6086a/OR-31-04-1547-g04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3975986/07854ff09d67/OR-31-04-1547-g05.jpg

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