Molecular Localization of Human Papilloma Viral 16/18 DNA in Adenoctomized Tissues from a group of Iraqi Patients
DOI:
https://doi.org/10.37506/mlu.v20i3.1545Keywords:
Adenoid hypertrophy; Nasopharyngeal adenotonsillar tissues; HPV 16/18; CISH.Abstract
Background: Low- and high- oncogenic risk human papilloma viral infections have been related to the
genesis of a variety of human benign and malignant tumors in the oral cavity and nasopharyngeal tissues.
High- risk types of human papilloma virus are now well established as major etiologic factors of head
and neck cancers, including tonsillar carcinomas. Objective: The current prospective case- control study
aimed to unravel the frequency of HPV genotype 16/18 DNA detection rates in the adenoctomized tissues
from patients with nasopharyngeal tonsillar adenoid hypertrophy. Materials and Method: A sixty (60)
nasal as well as nasopharyngeal adenotonsillar tissues obtained from patients with adenoid hypertrophy via
adenoctomies were enrolled. Forty (40) adenotonsillar tissues were from patients with adenoid hypertrophy,
and (20) normal nasal tissue specimens were obtained from pediatric patients following trimming operations
of inferior nasal turbinates’ with unremarkable pathological changes (as an apparently healthy control
group). A recent version of chromogenic in situ hybridization (CISH) method for HPV detection were
performed by using specified DNA probes for DNA of high- risk HPV 16/18 genotypes. Results: Among
nasopharyngeal adenotonsillar tissues group, 15 out of 40 have revealed positive CISH signals for DNA of
HPV 16 / 18 genotype, constituting 35% of the total screened adenoid hypertrophied tissues. No positive–
CISH reactions were detected in the control nasal tissues. Statistically, the results obtained in this study
showed significant difference when compared to the control tissues group. Conclusions: The significant rate
of such high- oncogenic HPV genotypes detection in those nasopharyngeal adenotonsillar tissues criticizes
searching its further importance, as HPV 16/18 genotypes are critically correlated to many pre- neoplastic
as well as malignant lesions.