Research Article

Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation

Volume: 2 Number: 2 October 8, 2019

Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation

Abstract

Objective: This study aims to understand the pathophysiology of bone and tissue remodeling by demonstrating the gene expression profiles in the development of chronic rhinosinusitis (CRS). Material and Methods: The study included patients who were operated with the diagnosis of CRS. The study group consisted of eight patients who underwent endoscopic sinus surgery with the diagnosis of CRS and had a history of chronic sinusitis as well as osteitic bone changes. The control group consisted of ethmoid bulla specimens of eight patients who had no history of sinusitis or sinus surgery with the diagnosis of acute sinusitis or antrochoanal polyp. In both bone and mucosal samples, RNA isolation was performed to identify and analyze genes that were upregulated and downregulated by whole-gene expression profiling using microarray technology. Results: When the diseased and healthy bone samples were compared, a total of 1302 genes were detected in 1766, and the disease was intact. Four genes, CD36 (FC[Fold Change]=31.19), tenascin XB (FC=13.6), S100 calcium binding protein A12 (FC=9.4), and G0/G1 switch 2 (FC=9.3) up-regulated in both bone and mucosa. Conclusion: Chronic rhinosinusitis is a disease that decreases both quality of life of the patient and the high cost of treatment. Gene expression analysis in tissue samples of patients with CRS and treatment-resistant CRS disease early can be used in the diagnosis of the period. With the understanding of the mechanisms involved in disease development, new treatment protocols can be established in the early period to prevent insufficiencies in medical and surgical treatment.

Keywords

References

  1. Gliklich RE, Metson R. Economic implications of chronic sinusitis. Otolaryngol Head Neck Surg 1998; 118: 344-9.
  2. Georgalas C. Osteitis and paranasal sinus inflammation: what we know and what we do not. Curr Opin Otolaryngol Head Neck Surg 2013; 21:45-49.
  3. Snidvongs K, McLachlan R, Sacks R, Earls P, Harvey RJ. Correlation of the Kennedy Osteitis Score to clinico-histologic features of chronic rhinosinusitis. Int Forum Allergy Rhinol 2013; 3: 369-75.
  4. Kennedy DW, Senior BA, Gannon FH, Montone KT, Hwang P, Lanza DC. Histology and Histomorphometry of Ethmoid Bone in Chronic Rhinosinusitis. Laryngoscope 1998; 108: 502-7.
  5. Bhandarkar ND, Sautter NB, Kennedy DW, Smith TL. Osteitis in chronic rhinosinusitis: a review of the literature. Int Forum Allergy Rhinol 2013; 3: 55-63.
  6. Xu Y, Wang J, Bao Y, Jiang W, Zuo L, Song D, et al. Identification of two antagonists of the scavenger receptor CD36 using a high-throughput screening model. Anal Biochem 2010; 400: 207-12.
  7. Zidi A, Castelló A, Jordana J, Carrizosa J, Urrutia B, Serradilla JM, et al. Identification of two paralogous caprine CD36 genes that display highly divergent mRNA expression profiles. Comp Immunol Microbiol Infect Dis 2013; 36:1-7.
  8. Inoue T, Kobayashi K, Inoguchi T, Sonoda N, Fujii M, Maeda Y, et al. Reduced expression of adipose triglyceride lipase enhances tumor necrosis factor alpha-induced intercellular adhesion molecule-1 expression in human aortic endothelial cells via protein kinase C-dependent activation of nuclear factor-kappaB. J Biol Chem 2011; 286: 32045-53.

Details

Primary Language

English

Subjects

Otorhinolaryngology

Journal Section

Research Article

Publication Date

October 8, 2019

Submission Date

September 30, 2019

Acceptance Date

October 7, 2019

Published in Issue

Year 2019 Volume: 2 Number: 2

APA
Günel, C., Bozkurt, G., & Akar, Y. C. (2019). Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation. European Journal of Rhinology and Allergy, 2(2), 35-40. https://doi.org/10.5152/ejra.2019.215
AMA
1.Günel C, Bozkurt G, Akar YC. Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation. Eur J Rhinol Allergy. 2019;2(2):35-40. doi:10.5152/ejra.2019.215
Chicago
Günel, Ceren, Gökay Bozkurt, and Yaşar Can Akar. 2019. “Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation”. European Journal of Rhinology and Allergy 2 (2): 35-40. https://doi.org/10.5152/ejra.2019.215.
EndNote
Günel C, Bozkurt G, Akar YC (October 1, 2019) Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation. European Journal of Rhinology and Allergy 2 2 35–40.
IEEE
[1]C. Günel, G. Bozkurt, and Y. C. Akar, “Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation”, Eur J Rhinol Allergy, vol. 2, no. 2, pp. 35–40, Oct. 2019, doi: 10.5152/ejra.2019.215.
ISNAD
Günel, Ceren - Bozkurt, Gökay - Akar, Yaşar Can. “Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation”. European Journal of Rhinology and Allergy 2/2 (October 1, 2019): 35-40. https://doi.org/10.5152/ejra.2019.215.
JAMA
1.Günel C, Bozkurt G, Akar YC. Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation. Eur J Rhinol Allergy. 2019;2:35–40.
MLA
Günel, Ceren, et al. “Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation”. European Journal of Rhinology and Allergy, vol. 2, no. 2, Oct. 2019, pp. 35-40, doi:10.5152/ejra.2019.215.
Vancouver
1.Ceren Günel, Gökay Bozkurt, Yaşar Can Akar. Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation. Eur J Rhinol Allergy. 2019 Oct. 1;2(2):35-40. doi:10.5152/ejra.2019.215

You can find the current version of the Instructions to Authors at: https://www.eurjrhinol.org/en/instructions-to-authors-104

Starting on 2020, all content published in the journal is licensed under the Creative Commons Attribution-NonCommercial (CC BY-NC) 4.0 International
License which allows third parties to use the content for non-commercial purposes as long as they give credit to the original work. This license
allows for the content to be shared and adapted for non-commercial purposes, promoting the dissemination and use of the research published in
the journal.
The content published before 2020 was licensed under a traditional copyright, but the archive is still available for free access.