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Identification of novel potential biomarkers and signaling pathways related to otitis media induced by diesel exhaust particle in in vivo system via transcriptomic analysis

Presenting Author: Moo Kyun Park

Published online by Cambridge University Press:  03 June 2016

So Young Kim ,
Hyo Jeong Kim ,
Jee Young Kwon ,
Yeo Jin Kim ,
Seung Hun Kang ,
Chong Sun Kim ,
Young Ho Kim ,
Jae-Jun Song ,
Young Rok Seo  and
Moo Kyun Park
So Young Kim
Affiliation:
CHA Bundang Medical Center, CHA University
Hyo Jeong Kim
Affiliation:
DonggukUniversity Biomedi Campus
Jee Young Kwon
Affiliation:
DonggukUniversity Biomedi Campus
Yeo Jin Kim
Affiliation:
DonggukUniversity Biomedi Campus
Seung Hun Kang
Affiliation:
DonggukUniversity Biomedi Campus
Chong Sun Kim
Affiliation:
Soree Ear Clinic
Young Ho Kim
Affiliation:
Seoul National University College of Medicine
Jae-Jun Song
Affiliation:
Korea University College of Medicine
Young Rok Seo
Affiliation:
DonggukUniversity Biomedi Campus
Moo Kyun Park
Affiliation:
Seoul National University College of Medicine
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Abstract

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Information
The Journal of Laryngology & Otology , Volume 130 , Supplement S3: Abstracts for the 10th International Conference on Cholesteatoma , May 2016 , pp. S190 - S191
Copyright
Copyright © JLO (1984) Limited 2016 

Learning Objectives: The aim of the present study was to discover potential molecular biomarkers and pathways triggered by DEP exposure in rodent model. Here, we conducted transcriptomic analysis to identify novel potential biomarkers in middle ears of DEP-exposed mice.

Introduction: Association between air pollutants and inflammatory diseases such as Otitis Media (OM) has been shown in recent studies. Diesel exhaust particle (DEP), one of major components among diverse air pollutants, is characterized by a carbonic mixture composed of polycyclic aromatic hydrocarbons (PAHs), nitro-PAHs, small amounts of sulfate, nitrate, metals, and other trace elements. The exposure to DEP as a risk factor for inflammatory diseases has been reported in several recent investigations. In line with these, our previous study identified potential biomarkers in in vitro system through gene expression microarray and pathway analysis. Although investigations in in vitro system have been conducted to elucidate plausible biomarkers and molecular mechanisms related with DEP, it is necessary to carry out in vivo study to identify exact biological relevance regarding incidence of OM caused by DEP exposure.

Methods: We conducted transcriptomic analysis to identify novel potential biomarkers in middle ears of DEP-exposed mice.

Results: A total of 697 genes were differentially expressed in the DEP-exposed mice; 424 genes and 273 genes were up-and down-regulated, respectively. In addition, signaling pathways among differentially expressed genes mediated by DEP exposure were predicted from different two point of view. Subsequently, we identified several key molecular biomarkers, CHRM1, EPO, SOS1, ESR1, CD4, and IFNA1.

Conclusions: In conclusion, our results might ascertain related cell process and signaling interacted genes underlying DEP exposure and its effects. Moreover, the discovered biomarkers can be recognized as potential candidates for developing early diagnosis and effective treatment strategies of DEP-mediated disorders.

Learning Objectives: We discovered potential molecular biomarkers and pathways triggered by DEP exposure in rodent model.