Razavi Nikoo Hadi, Ardebili Abdollah, Ravanshad Mehrdad, Rezaei Fatemeh, Teimoori Ali, Khanizadeh Sayyad, Pouriayevali Mohammad Hassan, Ajorloo Mehdi
Laboratory Science Research Center, Golestan University of Medical Sciences, Gorgan, Iran.
Department of Microbiology, Faculty of Medicine, Golestan University of Medical Sciences, Gorgan, Iran.
Iran Biomed J. 2017 Nov;21(6):411-6. doi: 10.18869/acadpub.ibj.21.6.411. Epub 2017 May 2.
Detection and quantification of human Papillomavirus (HPV) genome in oral carcinoma play an important role in diagnosis, as well as implications for progression of disease.
We evaluated tissues from 50 esopharyngeal cancers collected from different regions of Iran for HPV E6 using the two type-specific primers sets. E6 gene of HPV genotypes was amplified by specific primers. The sensitivity of PCR assay was analyzed and determined using HPV-DNA-containing plasmids. Real-time PCR was utilized to determine the prevalence and HPV viral load in patients with oral cavity squamous cell carcinoma.
Eighteen (36%) specimens were positive for HPV. Among the 18 positive specimens, 10 showed HPV-18 (55.55%), and 8 specimens were positive for HPV-11 (44.44%). Of the 18 infected specimens, 6 (33.32%) and 12 (66.65%) were identified as high-titer and low-titer viral load, respectively.
The PCR-based assay, developed in the current study, could be used for HPV detection, quantification, and genotyping in epidemiological and clinical studies.
检测和定量口腔癌中人乳头瘤病毒(HPV)基因组在诊断以及疾病进展的影响方面发挥着重要作用。
我们使用两种型特异性引物组评估了从伊朗不同地区收集的50例食管癌组织中的HPV E6。通过特异性引物扩增HPV基因型的E6基因。使用含HPV-DNA的质粒分析并确定PCR检测的灵敏度。利用实时PCR确定口腔鳞状细胞癌患者中HPV的患病率和病毒载量。
18例(36%)标本HPV呈阳性。在这18例阳性标本中,10例显示HPV-18(55.55%),8例标本HPV-11呈阳性(44.44%)。在这18例感染标本中,分别有6例(33.32%)和12例(66.65%)被鉴定为高滴度和低滴度病毒载量。
本研究中开发的基于PCR的检测方法可用于流行病学和临床研究中的HPV检测、定量和基因分型。