Integration of human papillomavirus type-16 and type-18 is a very early event in cervical carcinogenesis

被引:40
作者
Huang, L. -W [1 ,2 ,3 ]
Chao, S. -L [4 ]
Lee, B. -H [5 ]
机构
[1] Shin Kong Wu Ho Su Mem Hosp, Dept Obstet & Gynecol, Taipei 111, Taiwan
[2] Fu Jen Catholic Univ, Sch Med, Hsinchuang, Taipei Hsien, Taiwan
[3] Taipei Med Univ, Sch Med, Taipei, Taiwan
[4] Taipei City Hosp, Renai Branch, Dept Chinese Med, Taipei, Taiwan
[5] King Car Food Ins Co Ltd, Yuan Shan Res Inst, Ilan, Taiwan
关键词
D O I
10.1136/jcp.2007.052027
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Aim: Human papillomavirus (HPV) integration is a critical event in cervical carcinogenesis. The aim of this study was to explore the physical status of HPV-16 and HPV-18 during the progression of cervical precancerous lesions. Methods: A series of 101 HPV-16 or HPV-18 positive cervical neoplasms (32 cervical intraepithelial neoplasia (CIN) cases and 69 cervical carcinoma (CC) cases) were evaluated. The physical status of both types of HPV was assessed from paraffin-embedded formaldehyde-fixed surgical specimens by real-time PCR. Results: For HPV-16, integrated DNA was observed in 5 (83.3%) of 6 CIN I cases, 10 (90.9%) of 11 CIN II/III cases, 29 (82.9%) of 35 FIGO (International Federation of Gynecology and Obstetrics) stage I CC cases and 16 (94.1%) of 17 FIGO stages II similar to IV CC cases. For HPV-18, integrated DNA was observed in 3 (50%) of 6 CIN I cases, 5 (55.6%) of 9 CIN II/III cases, 9 (64.3%) of 14 FIGO stage I CC cases, and 1 (33.3%) of 3 FIGO stages II similar to IV CC cases. The mixed form of HPV DNA was the most prevalent physical state in HPV-16. There was no significant difference between the physical state of HPV-16 and HPV-18 DNA with regard to the various grades of cervical lesions. Conclusions: These data imply that integration of HPV-16 and HPV-18 DNA into the host genome occurs in the very early stage of cervical neoplastic progression. These early events may play an initiating role in the malignant transformation of HPV-16 and HPV-18-related low-grade lesions into high-grade dysplasia and invasive carcinoma.
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收藏
页码:627 / 631
页数:5
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