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增殖细胞核抗原(PCNA)表达及核DNA含量在早期声门癌放疗后复发预测中的作用

Proliferating cell nuclear antigen (PCNA) expression and nuclear DNA content in predicting recurrence after radiotherapy of early glottic cancer.

作者信息

Munck-Wikland E, Fernberg J O, Kuylenstierna R, Lindholm J, Auer G

机构信息

Department of Oto-rhino-laryngology, Karolinska Hospital, Stockholm, Sweden.

出版信息

Eur J Cancer B Oral Oncol. 1993 Jan;29B(1):75-9. doi: 10.1016/0964-1955(93)90014-6.

Abstract

Proliferating cell nuclear antigen (PCNA) is a DNA replication protein maximally elevated in late G1 and S phases of the cell cycle. By using monoclonal antibodies, the expression of PCNA can be quantified and the rate of tumour cell proliferation estimated. The degree of DNA aberration in a tumour cell population reflects its genetic instability and has been implicated as a prognostic factor in an increasing number of solid tumours. The nuclear DNA content can be assessed by densitometric image cytometry DNA analysis. Both PCNA and DNA analysis can be performed on histological sections from paraffin embedded biopsies. In search of efficient and reproducible methods to identify early glottic cancers with increased risk for recurrence after radiotherapy, the PCNA expression as well as the DNA content of the diagnostic biopsies from 28 T1N0M0 glottic cancers were assessed. The group of tumours which recurred locally after radiotherapy displayed lower PCNA expression and higher DNA aberration than the group of tumours which were cured. Moreover, a combination of both parameters improved the possibility to discriminate the two groups. For T1 glottic cancer displaying high grade of genetic instability or low grade of proliferation, treatment regimes other than radiotherapy and closer follow-ups could be considered.

摘要

增殖细胞核抗原(PCNA)是一种DNA复制蛋白,在细胞周期的G1晚期和S期表达量最高。通过使用单克隆抗体,可以对PCNA的表达进行定量,并估计肿瘤细胞的增殖速率。肿瘤细胞群体中的DNA畸变程度反映了其基因不稳定性,并且在越来越多的实体瘤中被认为是一种预后因素。细胞核DNA含量可通过密度图像细胞术DNA分析来评估。PCNA和DNA分析均可在石蜡包埋活检组织的组织切片上进行。为了寻找有效且可重复的方法来识别放疗后复发风险增加的早期声门癌,我们评估了28例T1N0M0声门癌诊断活检组织的PCNA表达以及DNA含量。放疗后局部复发的肿瘤组比治愈的肿瘤组显示出更低的PCNA表达和更高的DNA畸变。此外,这两个参数的组合提高了区分两组的可能性。对于显示出高度基因不稳定性或低增殖程度的T1声门癌,可考虑采用放疗以外的治疗方案并进行更密切的随访。

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