Analysis of human papilloma virus type 52 integration status in exfoliated cervical cells

被引:7
作者
Zhang, Ke [1 ]
Liu, Zhanjun [1 ]
Li, Ji [1 ]
Li, Juan [1 ]
Yan, Jianghong [1 ]
Su, Yunchuan [1 ]
Li, Shuying [1 ]
Li, Jintao [2 ]
机构
[1] North China Univ Sci & Technol, Hebei Key Lab Chron Dis, Tangshan Key Lab Preclin & Basic Res Chron Dis, Sch Basic Med Sci, 57 Jianshe South Rd, Tangshan 063000, Hebei, Peoples R China
[2] Beijing Univ Technol, Coll Life Sci & Bioengn, 100 Pingleyuan, Beijing 100124, Peoples R China
基金
北京市自然科学基金;
关键词
human papillomavirus; cervical lesions; infection; integration; VIRAL LOAD; INTRAEPITHELIAL NEOPLASIA; HPV INTEGRATION; CANCER; RISK; PCR; DNA; REPLICATION; PREVALENCE; SEQUENCES;
D O I
10.3892/etm.2017.5279
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To explore the significance of human papilloma virus type 52 (HPV52) infection and its integration in cells within cervical lesions, the expression levels of HPV52 were detected using polymerase chain reaction (PCR). The copy numbers of HPV52 E2, HPV52 E6 and the reference gene beta-actin were determined by quantitative PCR to analyze the association between HPV52 integration and cervical lesions. HPV52 integration was analyzed by the amplification of papillomavirus oncogene transcripts. A total of 13 samples from 468 cases were positive for HPV52. Among the samples, 1 case with an E2/E6 ratio >1 was purely episomal, 3 cases with an E2/E6 ratio of 0 were purely integrated, and 9 cases with an E2/E6 ratio of between 0 and 1 were a mixture of integrated and episomal. With the progression of cervical disease, the prevalence of the episomal type decreased gradually, and the prevalence of the integrated (episomal and integrated) forms increased. The pure integration of HPV52 occurred in chromosomes 2, 5 and 8. These results indicate that HPV52 integration into the host genome may be a key factor in cervical lesions. Thus, patients at high risk for cervical lesions may potentially be identified by screening for HPV52 infection and integration.
引用
收藏
页码:5817 / 5824
页数:8
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