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Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma

BACKGROUND: Nasopharyngeal carcinoma (NPC) is a malignant tumor which arises in surface epithelium of the posterior wall of the nasopharynx. There's is evidence that Epstein Barr virus (EBV) is associated to NPC development. However, many epidemiologic studies point to a connection between vira...

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Autores principales: Laantri, Nadia, Attaleb, Mohammed, Kandil, Mostafa, Naji, Fadwa, Mouttaki, Tarik, Dardari, R'kia, Belghmi, Khalid, Benchakroun, Nadia, El Mzibri, Mohammed, Khyatti, Meriem
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060847/
https://www.ncbi.nlm.nih.gov/pubmed/21352537
http://dx.doi.org/10.1186/1750-9378-6-3
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author Laantri, Nadia
Attaleb, Mohammed
Kandil, Mostafa
Naji, Fadwa
Mouttaki, Tarik
Dardari, R'kia
Belghmi, Khalid
Benchakroun, Nadia
El Mzibri, Mohammed
Khyatti, Meriem
author_facet Laantri, Nadia
Attaleb, Mohammed
Kandil, Mostafa
Naji, Fadwa
Mouttaki, Tarik
Dardari, R'kia
Belghmi, Khalid
Benchakroun, Nadia
El Mzibri, Mohammed
Khyatti, Meriem
author_sort Laantri, Nadia
collection PubMed
description BACKGROUND: Nasopharyngeal carcinoma (NPC) is a malignant tumor which arises in surface epithelium of the posterior wall of the nasopharynx. There's is evidence that Epstein Barr virus (EBV) is associated to NPC development. However, many epidemiologic studies point to a connection between viral infections by the human papillomavirus (HPV) and NPC. METHOD: Seventy Moroccan patients with NPC were screened for EBV and HPV. EBV detection was performed by PCR amplification of BZLF1 gene, encoding the ZEBRA (Z Epstein-Barr Virus Replication Activator) protein, and HPV infection was screened by PCR amplification with subsequent typing by hybridization with specific oligonucleotides for HPV types 16, 18, 31, 33, 35, 45 and 59. RESULTS: The age distribution of our patients revealed a bimodal pattern. Sixty two cases (88.9%) were classified as type 3 (undifferentiated carcinoma), 6 (8.6%) as type 2 (non keratinizing NPC) and only 2 (2.9%) cases were classified as type 1 (keratinizing NPC). EBV was detected in all NPC tumors, whereas HPV DNA was revealed in 34% of cases (24/70). Molecular analysis showed that 20.8% (5/24) were infected with HPV31, and the remaining were infected with other oncogenic types (i.e., HPV59, 16, 18, 33, 35 and 45). In addition, statistical analysis showed that there's no association between sex or age and HPV infection (P > 0.1). CONCLUSION: Our data indicated that EBV is commonly associated with NPC in Moroccan patients and show for the first time that NPC tumours from Moroccan patients harbour high risk HPV genotypes.
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spelling pubmed-30608472011-03-19 Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma Laantri, Nadia Attaleb, Mohammed Kandil, Mostafa Naji, Fadwa Mouttaki, Tarik Dardari, R'kia Belghmi, Khalid Benchakroun, Nadia El Mzibri, Mohammed Khyatti, Meriem Infect Agent Cancer Research Article BACKGROUND: Nasopharyngeal carcinoma (NPC) is a malignant tumor which arises in surface epithelium of the posterior wall of the nasopharynx. There's is evidence that Epstein Barr virus (EBV) is associated to NPC development. However, many epidemiologic studies point to a connection between viral infections by the human papillomavirus (HPV) and NPC. METHOD: Seventy Moroccan patients with NPC were screened for EBV and HPV. EBV detection was performed by PCR amplification of BZLF1 gene, encoding the ZEBRA (Z Epstein-Barr Virus Replication Activator) protein, and HPV infection was screened by PCR amplification with subsequent typing by hybridization with specific oligonucleotides for HPV types 16, 18, 31, 33, 35, 45 and 59. RESULTS: The age distribution of our patients revealed a bimodal pattern. Sixty two cases (88.9%) were classified as type 3 (undifferentiated carcinoma), 6 (8.6%) as type 2 (non keratinizing NPC) and only 2 (2.9%) cases were classified as type 1 (keratinizing NPC). EBV was detected in all NPC tumors, whereas HPV DNA was revealed in 34% of cases (24/70). Molecular analysis showed that 20.8% (5/24) were infected with HPV31, and the remaining were infected with other oncogenic types (i.e., HPV59, 16, 18, 33, 35 and 45). In addition, statistical analysis showed that there's no association between sex or age and HPV infection (P > 0.1). CONCLUSION: Our data indicated that EBV is commonly associated with NPC in Moroccan patients and show for the first time that NPC tumours from Moroccan patients harbour high risk HPV genotypes. BioMed Central 2011-02-25 /pmc/articles/PMC3060847/ /pubmed/21352537 http://dx.doi.org/10.1186/1750-9378-6-3 Text en Copyright ©2011 Laantri et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Laantri, Nadia
Attaleb, Mohammed
Kandil, Mostafa
Naji, Fadwa
Mouttaki, Tarik
Dardari, R'kia
Belghmi, Khalid
Benchakroun, Nadia
El Mzibri, Mohammed
Khyatti, Meriem
Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
title Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
title_full Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
title_fullStr Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
title_full_unstemmed Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
title_short Human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
title_sort human papillomavirus detection in moroccan patients with nasopharyngeal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3060847/
https://www.ncbi.nlm.nih.gov/pubmed/21352537
http://dx.doi.org/10.1186/1750-9378-6-3
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