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Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma

Infection with human papillomavirus (HPV) is a major risk factor for development of anal squamous cell carcinoma. Despite over 100 genotypes of the virus, HPV 16 and 18 are considered pathogenic as they are seen in the majority of cervical and anal cancers. We have employed a custom microarray to ex...

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Autores principales: Ramamoorthy, Sonia, Liu, Yu-Tsueng, Luo, Linda, Miyai, Katsumi, Lu, Qing, Carethers, John M
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964599/
https://www.ncbi.nlm.nih.gov/pubmed/20939896
http://dx.doi.org/10.1186/1750-9378-5-17
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author Ramamoorthy, Sonia
Liu, Yu-Tsueng
Luo, Linda
Miyai, Katsumi
Lu, Qing
Carethers, John M
author_facet Ramamoorthy, Sonia
Liu, Yu-Tsueng
Luo, Linda
Miyai, Katsumi
Lu, Qing
Carethers, John M
author_sort Ramamoorthy, Sonia
collection PubMed
description Infection with human papillomavirus (HPV) is a major risk factor for development of anal squamous cell carcinoma. Despite over 100 genotypes of the virus, HPV 16 and 18 are considered pathogenic as they are seen in the majority of cervical and anal cancers. We have employed a custom microarray to examine DNA for several HPV genotypes. We aimed to determine the accuracy of our microarray in anal cancer DNA for HPV genotypes compared to the DNA sequencing gold standard. METHODS: We utilized a sensitive microarray platform to classify 37 types of mucosal HPVs including 14 known high-risk and 23 low-risk types based on cervical cancer data. We utilized DNA from pathologically confirmed cases of anal squamous cell carcinoma. All samples underwent microarray HPV genotyping and PCR analysis. RESULTS: HPV was detected in 18/20 (90%) anal cancers. HPV genotypes 16 and 18 were present in the majority of specimens, with HPV 16 being the most common. Eighty percent of anal cancers had at least two HPV types. Ten percent of cases (2/20) tested negative using our microarray; DNA sequencing confirmed the lack of presence of HPV DNA in these samples. CONCLUSIONS: Microarray technology is an accurate way to screen for various genotypes of HPV in anal cancer, with 100% correlation with genomic DNA detection of HPV. The majority of anal cancers in our study associated with pathogenic HPV 16 and/or 18. Other HPV genotypes are present simultaneously with HPV 16 and 18, and might contribute to its pathogenesis.
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spelling pubmed-29645992010-10-28 Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma Ramamoorthy, Sonia Liu, Yu-Tsueng Luo, Linda Miyai, Katsumi Lu, Qing Carethers, John M Infect Agent Cancer Research Article Infection with human papillomavirus (HPV) is a major risk factor for development of anal squamous cell carcinoma. Despite over 100 genotypes of the virus, HPV 16 and 18 are considered pathogenic as they are seen in the majority of cervical and anal cancers. We have employed a custom microarray to examine DNA for several HPV genotypes. We aimed to determine the accuracy of our microarray in anal cancer DNA for HPV genotypes compared to the DNA sequencing gold standard. METHODS: We utilized a sensitive microarray platform to classify 37 types of mucosal HPVs including 14 known high-risk and 23 low-risk types based on cervical cancer data. We utilized DNA from pathologically confirmed cases of anal squamous cell carcinoma. All samples underwent microarray HPV genotyping and PCR analysis. RESULTS: HPV was detected in 18/20 (90%) anal cancers. HPV genotypes 16 and 18 were present in the majority of specimens, with HPV 16 being the most common. Eighty percent of anal cancers had at least two HPV types. Ten percent of cases (2/20) tested negative using our microarray; DNA sequencing confirmed the lack of presence of HPV DNA in these samples. CONCLUSIONS: Microarray technology is an accurate way to screen for various genotypes of HPV in anal cancer, with 100% correlation with genomic DNA detection of HPV. The majority of anal cancers in our study associated with pathogenic HPV 16 and/or 18. Other HPV genotypes are present simultaneously with HPV 16 and 18, and might contribute to its pathogenesis. BioMed Central 2010-10-12 /pmc/articles/PMC2964599/ /pubmed/20939896 http://dx.doi.org/10.1186/1750-9378-5-17 Text en Copyright ©2010 Ramamoorthy 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
Ramamoorthy, Sonia
Liu, Yu-Tsueng
Luo, Linda
Miyai, Katsumi
Lu, Qing
Carethers, John M
Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma
title Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma
title_full Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma
title_fullStr Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma
title_full_unstemmed Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma
title_short Detection of Multiple Human Papillomavirus Genotypes in Anal Carcinoma
title_sort detection of multiple human papillomavirus genotypes in anal carcinoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2964599/
https://www.ncbi.nlm.nih.gov/pubmed/20939896
http://dx.doi.org/10.1186/1750-9378-5-17
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