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子宫颈癌前病变和浸润性病变中HPV16、18、31及35型DNA的分析

Analysis of HPV16, 18, 31, and 35 DNA in pre-invasive and invasive lesions of the uterine cervix.

作者信息

Pirami L, Giachè V, Becciolini A

机构信息

Department of Clinical Physiopathology, University of Florence, Italy.

出版信息

J Clin Pathol. 1997 Jul;50(7):600-4. doi: 10.1136/jcp.50.7.600.

Abstract

AIMS

To analyse the physical state of different human papillomavirus (HPV) DNAs in 55 intraepithelial and invasive HPV associated cervical neoplasms.

METHODS

Restriction analysis, using a panel of five HPV type specific enzymes, was carried out for each sample; this was followed by Southern blot analysis.

RESULTS

Six (25%) of 24 cervical intraepithelial neoplasms had integrated DNA of different HPV types. In contrast, integration was detected in 25 (81%) of 31 cervical carcinomas. Tumour samples revealed differences in the integration profile of HPV16 and the other HPV types. Six (26%) of 23 HPV16 associated cancers contained only episomal DNA. In contrast, all eight tumours containing HPV18, 31, or 35 revealed integrated DNA exclusively.

CONCLUSIONS

The results suggest that in advanced cervical intraepithelial neoplasia lesions, a subset of lesions can be identified in which the viral genome is integrated and there is a greater risk of malignant progression. In addition, HPV16 DNA was not present in the integrated form in 26% of tumours, suggesting that integration and subsequent inactivation of the transcriptional regulator, E2, are not essential steps for the development of HPV16 associated carcinoma. In this respect, the behaviour of HPV16 associated tumours is different from HPV18, 31, and 35 associated tumours, where the viral genome is always present in the integrated form.

摘要

目的

分析55例上皮内和浸润性人乳头瘤病毒(HPV)相关宫颈肿瘤中不同HPV DNA的物理状态。

方法

对每个样本使用一组五种HPV型特异性酶进行限制性分析,随后进行Southern印迹分析。

结果

24例宫颈上皮内瘤变中有6例(25%)存在不同HPV型的整合DNA。相比之下,31例宫颈癌中有25例(81%)检测到整合。肿瘤样本显示HPV16与其他HPV型在整合模式上存在差异。23例与HPV16相关的癌症中有6例(26%)仅含有游离DNA。相比之下,所有8例含有HPV18、31或35的肿瘤均仅显示整合DNA。

结论

结果表明,在晚期宫颈上皮内瘤变病变中,可识别出一部分病毒基因组发生整合且恶性进展风险更高的病变。此外,26%的肿瘤中HPV16 DNA并非以整合形式存在,这表明转录调节因子E2的整合及随后的失活并非HPV16相关癌发生的必要步骤。在这方面,HPV16相关肿瘤的行为不同于HPV18、31和35相关肿瘤,后者病毒基因组总是以整合形式存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/67d3/500071/f381e4ee4501/jclinpath00256-0068-a.jpg

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