Abstract
The study objective is to evaluate the prevalence of Epstein—Barr virus (EBV), herpes virus, human papillomavirus (HPV), and cytomegalovirus (CMV) infection among patients with cancer of the nasal cavity and paranasal sinuses in the Arkhangelsk Region.Materials and methods. We examined surgical specimens from 100 patients treated in the Arkhangelsk Clinical Oncology Dispensary between 2010 and 2015. Tissue homogenates were used for DNA isolation. DNA amplification with subsequent detection was performed using polymerase chain reaction.Results and conclusion. The 36 % of study participants were infected with EBV; the second most common viral pathogens were CMV and human herpes virus type 6 (HHV-6), both found in 21 % of cases. Monoinfection was observed in less than one-third of patients (20 % — EBV, HPV type 16 — 6 %), whereas the remaining participants had mixed infections: EBV + HHV-6 (2 %), CMV + EBV (5 %), EBV + herpes simplex virus types 1 and 2 (HSV-1,2) (1 %), EBV + CMV + HHV-6 (3 %), HPV type 16 + HSV-1,2 (3 %), and HPV type 6 + HPV type 16 (7 %). None of the patients with stage I cancer had mixed infections, whereas participants with stage II, III, and IV cancer demonstrated mixed infections in 1 %, 11 %, and 9 % of cases respectively.After specific treatment, 11 patients (30.5 %) infected with EBV developed regional metastases and 5 patients (13.9 %) had relapses. All patients simultaneously infected with EBV and HHV-6 had distant metastases. Combination of EBV, CMV, and HHV-6 resulted in relapses in 100 % of cases and distant metastasis in 75 % of cases.
Highlights
The study objective is to evaluate the prevalence of Epstein
We examined surgical specimens from 100 patients treated in the Arkhangelsk Clinical Oncology Dispensary
Tissue homogenates were used for DNA isolation
Summary
Для молекулярно-биологического анализа проводили забор образцов из операционного материала. Из гомогената ткани опухоли выделяли ДНК вирусов с использованием набора реагентов MagNa Pure Compact Nucleic Acid Isolation Kit I–Large Volume на приборе MagNa Pure Compact (Roche, Швейцария). Амплификацию с последующей детекцией ДНК проводили методом ПЦР с гибридизационно-флуоресцентной детекцией в режиме реального времени на термоциклере Rotor Gene 6000 (Qiagen, Германия). Определяли ДНК ВПЧ высокого канцерогенного риска (16, 18, 31, 33, 35, 39, 45, 51, 52, 56, 58, 59-го типов) и низкого канцерогенного риска (6-го и 11-го типов), вируса простого герпеса 1-го и 2-го типов, ЦМВ, ВЭБ и вируса герпеса человека 6-го типа. Различия между изучаемыми группами были оценены с помощью параметрических (t-критерия Стьюдента для независимых выборок) и непараметрических (U-критерия Манна–Уитни) методов для количественных величин. Различия считали статистически значимыми при р
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