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Association of EBV and HPV co-infection with the development of cervical cancer in ethnic Uyghur women
1Department of Gynecology, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China
2Department of Gynecology, the General Hospital of Xinjiang Uyghur Autonomous Region, Urumqi, China
3Department of Biochemistry and Molecular Biology, Xinjiang Medical University, Urumqi, China
4Key Research Laboratory of Molecular Biology for Endemic Diseases, Xinjiang Medical University, Urumqi, China
*Corresponding Author(s): A. Abudula E-mail: abulizi_a@126.com
Objective: Study on the role of Epstein-Barr virus (EBV) and human papillomavirus (HPV) infection in the development of cervical cancer. Materials and Methods: We collected 178 cases of cervical tissue specimens of Uyghur women with cervicitis, cervical intraepithelial neoplasia (CIN I, CIN II-III), and cervical squamous cell carcinoma (CSCC). EBV- and HPV-DNA were detected by PCR of tissue DNA. EBV protein expression was checked by immunohistochemistry. Results: HPV-DNA was detectable in 2.5, 12.5, 68.0, and 96.4% of cases of cervicitis, CIN I, CIN II- III, and cervical cancer, respectively. For EBV-DNA, these numbers were 0, 3.1, 28.0, and 69.6%. There was a significant difference between the groups of cervicitis, CIN II-III, and cancer with respect to both HPV and EBV positivity rates (p < 0.05). Further analysis indicated that cervical lesion pathogenesis was not only accompanied by a gradually increasing rate of HPV or EBV-DNA alone, but also by an increasing rate of HPV-EBV dual infection (r = 0.46; p < 0.01). EBV protein expression was positive in 89.7% of EBV-DNA positive cases (34/39) and 6% of EBV-DNA negative cases (1/17). Conclusion: Cervical cancer development and progression may be closely associated with the dual-infection by HPV and EBV.
A. Abudoukadeer,M. Niyazi,A. Aikula,M. Kamilijiang,X. Sulaiman,A. Mutailipu,A. Abudula. Association of EBV and HPV co-infection with the development of cervical cancer in ethnic Uyghur women. European Journal of Gynaecological Oncology. 2015. 36(5);546-550.
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