Title of article
E6-Specific Detection and Typing of Human Papillomaviruses in Oral Cavity Specimens from Iranian Patients
Author/Authors
Razavi Nikoo, h. Laboratory Science Research Center - Golestan University of Medical Sciences - Gorgan, Iran , ardebili, a. Laboratory Science Research Center - Golestan University of Medical Sciences - Gorgan, Iran , ravanshad , m. Department of Virology - Faculty of Medical Sciences - Tarbiat Modares University - Tehran, Iran , rezaei, f. Department of Virology - Faculty of Medical Sciences - Tarbiat Modares University - Tehran, Iran , teimoori , a. Health Research Institute - Infectious and Tropical Diseases Research Center - Ahvaz Jundishapur University of Medical Sciences - Ahvaz, Iran , ajorloo, m. Hepatitis Research Center - Lorestan University of Medical Sciences - Khorramabad, Iran , khanizadeh, s. Hepatitis Research Center - Lorestan University of Medical Sciences - Khorramabad, Iran , pouriayevali, m.h. Department of Hepatitis and AIDS - Pasteur Institute of Iran - Tehran, Iran
Pages
6
From page
411
To page
416
Abstract
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. Methods: 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. Results: 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. Conclusions: The PCR-based assay, developed in the
current study, could be used for HPV detection, quantification, and genotyping in epidemiological and clinical
studies.
Keywords
Iran , Genotyping , Real-time PCR
Journal title
Iranian Biomedical Journal(IBJ)
Serial Year
2017
Record number
2525086
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