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Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa

Infectious agents have been identified as a major cause of specific types of human cancers worldwide. Several microorganisms have been identified as potential aggravators of ocular adnexal neoplasms; however, given the rarity of these neoplasms, large epidemiological studies are difficult to coordin...

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Autores principales: Usui, Yoshihiko, Rao, Narsing A., Takase, Hiroshi, Tsubota, Kinya, Umazume, Kazuhiko, Diaz-Aguilar, Daniel, Kezuka, Takeshi, Mochizuki, Manabu, Goto, Hiroshi, Sugita, Sunao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103257/
https://www.ncbi.nlm.nih.gov/pubmed/27830722
http://dx.doi.org/10.1038/srep36621
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author Usui, Yoshihiko
Rao, Narsing A.
Takase, Hiroshi
Tsubota, Kinya
Umazume, Kazuhiko
Diaz-Aguilar, Daniel
Kezuka, Takeshi
Mochizuki, Manabu
Goto, Hiroshi
Sugita, Sunao
author_facet Usui, Yoshihiko
Rao, Narsing A.
Takase, Hiroshi
Tsubota, Kinya
Umazume, Kazuhiko
Diaz-Aguilar, Daniel
Kezuka, Takeshi
Mochizuki, Manabu
Goto, Hiroshi
Sugita, Sunao
author_sort Usui, Yoshihiko
collection PubMed
description Infectious agents have been identified as a major cause of specific types of human cancers worldwide. Several microorganisms have been identified as potential aggravators of ocular adnexal neoplasms; however, given the rarity of these neoplasms, large epidemiological studies are difficult to coordinate. This study aimed to conduct an exhaustive search for pathogenic DNA in lymphoproliferative disorders (LPD) of the ocular adnexa in a total of 70 patients who were diagnosed with LPD of the ocular adnexa between 2008 and 2013. Specimens were screened for bacterial, viral, fungal, and parasitic DNA by multiplex polymerase chain reaction (PCR) and quantitative real-time PCR. Among cases of conjunctival mucosa-associated lymphoid tissue lymphoma, human herpes virus (HHV)-6, HHV-7, chlamydia, Epstein-Barr virus (EBV) and bacterial 16S ribosomal DNA were detected. In cases of IgG4-related ocular disease, similar pathogens were detected but in a larger number of patients. Our PCR assays detected DNAs of various infectious agents in tumor specimens, especially HHV6, HHV7, and EBV, with different positive rates in various types of LPD. Chronic inflammatory stimulation or activation of oncogenes from these infectious agents might be involved in the pathogenesis of LPD of the ocular adnexa.
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spelling pubmed-51032572016-11-17 Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa Usui, Yoshihiko Rao, Narsing A. Takase, Hiroshi Tsubota, Kinya Umazume, Kazuhiko Diaz-Aguilar, Daniel Kezuka, Takeshi Mochizuki, Manabu Goto, Hiroshi Sugita, Sunao Sci Rep Article Infectious agents have been identified as a major cause of specific types of human cancers worldwide. Several microorganisms have been identified as potential aggravators of ocular adnexal neoplasms; however, given the rarity of these neoplasms, large epidemiological studies are difficult to coordinate. This study aimed to conduct an exhaustive search for pathogenic DNA in lymphoproliferative disorders (LPD) of the ocular adnexa in a total of 70 patients who were diagnosed with LPD of the ocular adnexa between 2008 and 2013. Specimens were screened for bacterial, viral, fungal, and parasitic DNA by multiplex polymerase chain reaction (PCR) and quantitative real-time PCR. Among cases of conjunctival mucosa-associated lymphoid tissue lymphoma, human herpes virus (HHV)-6, HHV-7, chlamydia, Epstein-Barr virus (EBV) and bacterial 16S ribosomal DNA were detected. In cases of IgG4-related ocular disease, similar pathogens were detected but in a larger number of patients. Our PCR assays detected DNAs of various infectious agents in tumor specimens, especially HHV6, HHV7, and EBV, with different positive rates in various types of LPD. Chronic inflammatory stimulation or activation of oncogenes from these infectious agents might be involved in the pathogenesis of LPD of the ocular adnexa. Nature Publishing Group 2016-11-10 /pmc/articles/PMC5103257/ /pubmed/27830722 http://dx.doi.org/10.1038/srep36621 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Usui, Yoshihiko
Rao, Narsing A.
Takase, Hiroshi
Tsubota, Kinya
Umazume, Kazuhiko
Diaz-Aguilar, Daniel
Kezuka, Takeshi
Mochizuki, Manabu
Goto, Hiroshi
Sugita, Sunao
Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa
title Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa
title_full Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa
title_fullStr Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa
title_full_unstemmed Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa
title_short Comprehensive polymerase chain reaction assay for detection of pathogenic DNA in lymphoproliferative disorders of the ocular adnexa
title_sort comprehensive polymerase chain reaction assay for detection of pathogenic dna in lymphoproliferative disorders of the ocular adnexa
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5103257/
https://www.ncbi.nlm.nih.gov/pubmed/27830722
http://dx.doi.org/10.1038/srep36621
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