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口腔癌旁非肿瘤上皮中 Ki-67 的表达作为多发性口腔肿瘤的风险标志物。

Ki-67 expression in non-tumour epithelium adjacent to oral cancer as risk marker for multiple oral tumours.

机构信息

Oral Medicine Department, School of Dentistry, University of Granada, Granada, Spain.

出版信息

Oral Dis. 2010 Jan;16(1):68-75. doi: 10.1111/j.1601-0825.2009.01611.x. Epub 2009 Aug 4.

Abstract

OBJECTIVE

The aim of this study was to determine whether the differential assessment of epithelial proliferation is useful to diagnose premalignant fields and assess the risk of multiple tumours.

MATERIAL AND METHODS

We analysed 83 oral carcinomas with associated non-tumour epithelium classified as distant or close according to its distance (> or <1 cm) from the invasion point, and as squamous hyperplasia, mild, moderate, severe dysplasia or carcinoma in situ. Twenty-five healthy oral mucosa samples were used as controls. An immunohistochemical technique was applied using Mib-1. Ki-67 in premalignant epithelium was assessed in basal layer, parabasal layer, medium and upper third.

RESULTS

Parabasal expression was significantly higher or showed a tendency to be higher in close and distant epithelia with any histological grade than in the controls. Parabasal Ki-67 significantly differed between distant epithelia associated with multiple vs single tumours (P < 0.001) and between distant epithelia associated with multiple tumours vs controls (P < 0.001). This difference was not observed between distant epithelia associated with single tumours and controls (P = 0.175). The cut-off point that differentiated epithelia associated with multiple tumours was >50% of Ki-67 + parabasal cells in distant epithelia, which yielded 0.88 sensitivity and 0.79 specificity.

CONCLUSIONS

The concept of a precancerous field may be linked to an increase in the proliferative activity of parabasal cells.

摘要

目的

本研究旨在确定上皮细胞增殖的差异评估是否有助于诊断癌前病灶并评估多发肿瘤的风险。

材料与方法

我们分析了 83 例伴发非肿瘤上皮的口腔癌,根据其与侵袭点的距离(>1cm 或<1cm)将其分为远处和近处,并根据鳞状上皮增生、轻度、中度、重度异型增生或原位癌进行分类。25 例健康口腔黏膜标本作为对照。采用 Mib-1 免疫组织化学技术。在基底细胞层、副基底细胞层、中层和上三分之一层评估癌前上皮中的 Ki-67。

结果

与对照组相比,任何组织学分级的近旁和远处上皮的副基底表达均显著升高或有升高趋势。远处上皮中与单发肿瘤相比,多发肿瘤(P<0.001)和与对照组相比(P<0.001)的 Ki-67 副基底差异显著。单发肿瘤与对照组之间未观察到这种差异(P=0.175)。区分多发肿瘤相关远处上皮的截点为 Ki-67+副基底细胞>50%,其敏感性为 0.88,特异性为 0.79。

结论

癌前病灶的概念可能与副基底细胞增殖活性的增加有关。

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