4.5 Article

Detection and Genotyping of Human Papillomavirus (HPV16/18), Epstein-Barr Virus (EBV), and Human Cytomegalovirus (HCMV) in Endometrial Endometroid and Ovarian Cancers

Journal

PATHOGENS
Volume 12, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/pathogens12030397

Keywords

human papillomavirus; Epstein-Barr virus; human cytomegalovirus; ovarian cancer; endometrioid endometrial cancer

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The purpose of this study was to evaluate the relationship between HPV16/18, EBV, and HCMV infections and ovarian cancer. Real-time PCR was used to detect HPV, EBV, and HCMV in tumor tissue and normal tissue of the participants. The results showed that HCMV infection was significantly associated with an increased risk of endometrial cancer, while HPV16, HPV18, and EBV were associated with a higher risk of ovarian cancer.
The purpose of this study was to evaluate the relationship between human papillomavirus (HPV16/18), Epstein-Barr virus (EBV), and human cytomegalovirus (HCMV) infections and the occurrence of ovarian cancer in 48 women, of whom 36 underwent surgery and chemotherapy (group A), 12 in whom surgery was sufficient (group B), and 60 with endometroid endometrial cancer stage G1-G3 (group C), compared to patients in whom the uterus and its appendages were removed for nononcological reasons (control group). The detection of HPV, EBV, and HCMV in tumor tissue and normal tissue was performed using the real-time polymerase chain reaction (RT-PCR) technique. A statistically significantly higher risk of endometrial cancer was noted in patients infected only with HCMV (OR > 1; p < 0.05). In contrast, a significantly higher risk of ovarian cancer in group A was associated with HPV16, HPV18, and EBV (OR > 1; p < 0.05); a significantly higher risk of ovarian cancer in group B was associated with HPV18 and HMCV (OR > 1; p < 0.05). The obtained results suggest that HCMV infection is associated with the development of a stage of ovarian cancer when treatment can be completed with surgery alone. Meanwhile, EBV appears to be responsible for the development of ovarian cancer in more advanced stages.

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