Truong Phuong Kim, Lao Thuan Duc, LE Thuy Ai Huyen
Dept. of Molecular and Environmental Biotechnology, Faculty of Biology and Biotechnology, University of Science, Vietnam National University, Ho Chi Minh, Vietnam.
Dept. of Pharmaceutical and Medical Biotechnology, Faculty of Biotechnology, Ho Chi Minh City Open University, Ho Chi Minh, Vietnam.
Iran J Public Health. 2018 Mar;47(3):350-356.
The infection of human papillomavirus (HPV) has been considered as the common cause of cervical cancer, which is the leading cause of cancer death in women, in Vietnam. Recently, hypermethylation at tumor suppressor genes (TSGs) has been also demonstrated to be an early epigenetic event and cofactor in human cancer, including cancer of cervix. This study evaluated the frequency of gene promoter hyper-methylation status as well as whether did or not an association between patterns of DNA hypermethylation and high-risk HPV infection, led to risk of cervical cancer.
Methylation-Specific-PCR (MSP) was performed to analyze hypermethylation status from 109 liquid-based Papanicolaou test samples, archived and admitted from the Medic Medical Center and Au Lac Clinic Laboratory, Vietnam, from 2011-2014, a kind of non-invasive samples identified whether HPV/or non-HPV, high-risk/low-risk HPV infection.
promoter was differentially methylated in 50% cases of high-risk HPV genotype 16 and 18 infected samples. In contrast, a low frequency of hypermethylated DcR1 promoter was found in low risk HPV genotype infected sample (16.0%), and non-HPV infected sample (14.6%). A trend toward positive association was found between hypermethylation of DcR1 gene and HPV exposure was observed (=0.0005). Moreover, the odds ratio (OR) and relative risk (RR) were found in statistical significant value (OR=5.63 (95%CI = 2.25 - 14.07, <0.01), RR=3.31 (95%CI = 1.75 - 6.26, <0.01)).
The hypermethylation of 1 gene promoter is a significant characteristic of high-risk HPV infected samples in Vietnamese cervical patients. The OR and RR values showed that the strong correlation between hypermethylation and high-risk HPV infection, in which increased the risk of cervical cancer. The combination of hypermethylation and HPV detection based biomarker could be used in noninvasive samples obtained from high-risk cancer patients, offer significant practical advantages.
人乳头瘤病毒(HPV)感染被认为是越南宫颈癌的常见病因,而宫颈癌是该国女性癌症死亡的主要原因。最近,肿瘤抑制基因(TSG)的高甲基化也被证明是人类癌症(包括宫颈癌)中的一种早期表观遗传事件和辅助因子。本研究评估了基因启动子高甲基化状态的频率,以及DNA高甲基化模式与高危HPV感染之间是否存在关联,进而导致宫颈癌风险。
采用甲基化特异性PCR(MSP)分析了2011年至2014年期间从越南Medic医疗中心和Au Lac临床实验室存档并接收的109份液基巴氏试验样本的高甲基化状态,这是一种用于鉴定是否感染HPV/或未感染HPV、高危/低危HPV感染的非侵入性样本。
在50%的高危HPV基因型16和18感染样本中,启动子存在差异甲基化。相比之下,在低危HPV基因型感染样本(16.0%)和未感染HPV样本(14.6%)中,DcR1启动子高甲基化的频率较低。观察到DcR1基因高甲基化与HPV暴露之间存在正相关趋势(P=0.0005)。此外,发现优势比(OR)和相对风险(RR)具有统计学显著值(OR=5.63(95%CI=2.25-14.07,P<0.01),RR=3.31(95%CI=1.75-6.26,P<0.01))。
1基因启动子的高甲基化是越南宫颈癌患者高危HPV感染样本的一个显著特征。OR和RR值表明高甲基化与高危HPV感染之间存在强相关性,从而增加了宫颈癌风险。基于高甲基化和HPV检测的生物标志物组合可用于从高危癌症患者获得的非侵入性样本,具有显著的实际优势。