Zhang Qian, Dong Li, Hu Shangying, Feng Ruimei, Zhang Xun, Pan Qinjing, Ma Junfei, Zhang Li, Zhao Xuelian, Sankaranarayanan Rengaswamy, Qiao Youlin, Zhao Fanghui
Department of Epidemiology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Department of Pathology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Int J Cancer. 2017 Sep 15;141(6):1110-1119. doi: 10.1002/ijc.30807. Epub 2017 Jun 21.
E6 oncoprotein is a necessary agent of HPV driven oncogenic transformation. This study is aimed at evaluating the risk stratification potency of HPV 16/18 E6 oncoprotein (E6) as a triage method for HPV positivity. Moreover, it also acts as a predictor of cervical intraepithelial neoplasia grade 3 or worse (CIN3+). The screening cohort of 1,997 women was followed for a 15 year period in approximate five-year intervals. Participants were concurrently screened by HPV DNA testing (HC2), liquid based cytology (LBC), visual inspection with acetic acid (VIA) and were referred to colposcopy and biopsy if any tests reflected positive. E6 was performed on cervical samples collected from this cohort in 2005 and 2014. The ability of E6 to predict CIN3+ risk after the five- and ten-year interval was evaluated. Among HPV positive women in 2005, E6 indicated the lowest positive rate (9.9%) compared to LBC (48.4%) and VIA (28.0%), however, a higher prevalence rate (10.3%) and 10-year cumulative incidence rate (53.0%) of CIN3+ were detected among women who were E6 positive. Meanwhile, only 4.2% and 2.9% of women with abnormal LBC and positive VIA were diagnosed as prevalent CIN3+ in 2005, 23.0% and 16.5% developed to CIN3+ after year 10, respectively. Strong associations were found between precedent and subsequent HPV persistence and E6 oncoprotein expression (OR = 40.0 and 21.2, respectively). E6 oncoprotein could serve as a low-cost, highly specific, strongly indicative point-of-care method in the triage and treatment of HPV positive women.
E6癌蛋白是HPV驱动的致癌转化的必要因子。本研究旨在评估HPV 16/18 E6癌蛋白(E6)作为HPV阳性分流方法的风险分层效力。此外,它还可作为宫颈上皮内瘤变3级或更严重病变(CIN3+)的预测指标。对1997名女性的筛查队列进行了为期15年的随访,随访间隔约为五年。参与者同时接受HPV DNA检测(HC2)、液基细胞学检查(LBC)、醋酸肉眼观察(VIA),如果任何一项检测呈阳性,则转诊至阴道镜检查和活检。2005年和2014年对该队列收集的宫颈样本进行了E6检测。评估了E6在五年和十年间隔后预测CIN3+风险的能力。在2005年HPV阳性的女性中,与LBC(48.4%)和VIA(28.0%)相比,E6的阳性率最低(9.9%),然而,在E6阳性的女性中,CIN3+的患病率(10.3%)和10年累积发病率(53.0%)更高。同时,2005年LBC异常和VIA阳性的女性中分别只有4.2%和2.9%被诊断为CIN3+,10年后分别有23.0%和16.5%发展为CIN3+。在前瞻性和后续HPV持续感染与E6癌蛋白表达之间发现了强关联(OR分别为40.0和21.2)。E6癌蛋白可作为一种低成本、高特异性、强指示性的即时护理方法,用于HPV阳性女性的分流和治疗。