Gene Expression Analysis of Tissue Remodeling in Chronic Rhinosinusitis: A Preliminary Investigation
Year 2019,
Volume: 2 Issue: 2, 35 - 40, 08.10.2019
Ceren Günel
,
Gökay Bozkurt
,
Yaşar Can Akar
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.
References
-
Gliklich RE, Metson R. Economic implications of chronic sinusitis. Otolaryngol Head Neck Surg 1998; 118: 344-9.
-
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.
-
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.
-
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.
-
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.
-
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.
-
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.
-
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.
-
Erdman LK, Cosio G, Helmers AJ, Gowda DC, Grinstein S, Kain KC. CD36 and TLR interactions in inflammation and phagocytosis: implications for malaria. J Immunol 2009; 183: 6452-9.
-
Di Gioia M, Zanoni I. Toll-like receptor co-receptors as master regulators of the immune response. Mol Immunol 2015; 63:143-52.
-
Yuan Y, Nymoen DA, Stavnes HT, Rosnes AK, Bjørang O, Wu C, et al. Tenascin-X is a novel diagnostic marker of malignant mesothelioma. Am J Surg Pathol 2009; 33: 1673-82.
-
Matsumoto K, Takayama N, Ohnishi J, Ohnishi E, Shirayoshi Y, Nakatsuji N, et al. Tumour invasion and metastasis are promoted in mice deficient in tenascin-X. Genes Cells 2001; 6: 1101-11.
-
Liu Z, You XJ, Zhang S, Gao QX, Cui YH. Relationship between the expression of tenascin C and TGF-beta in human nasal polyp tissues. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi 2005; 40: 452-7.
-
Liu Z, Lu X, Wang H, Gao Q, Cui Y. The up-regulated expression of tenascin C in human nasal polyp tissues is related to eosinophil-derived transforming growth factor beta. Am J Rhinol 2006; 20: 629-633.
-
Payne SC, Han JK, Huyett P, Negri J, Kropf EZ, Borish L, et al. Microarray analysis of distinct gene transcription profiles in non-eosinophilic chronic sinusitis with nasal polyps. Am J Rhinol 2008; 22: 568-81.
-
Pietzsch J, Hoppmann S. Human S100A12: a novel key player in inflammation? Amino Acids 2009; 36: 381-9.
-
Garcia AF, Lopes JL, Costa-Filho AJ, Wallace BA, Araujo AP. Membrane interactions of S100A12 (Calgranulin C). PLoS One 2013; 8: https://doi.org/10.1371/journal.pone.0082555.
-
Foell D, Wittkowski H, Kessel C, Lüken A, Weinhage T, Varga G, et al. Proinflammatory S100A12 can activate human monocytes via Toll-like receptor 4. Am J Respir Crit Care Med 2013; 187: 1324-34.
-
Heckmann BL, Heckmann BL, Zhang X, Xie X, Liu J. The G0/G1 switch gene 2 (G0S2): Regulating metabolism and beyond. Biochim Biophys Acta 2013; 1831: 276-81.
-
Jin D, Sun J, Huang J, He Y, Yu A, Yu X, et al. TNF-α reduces g0s2 expression and stimulates lipolysis through PPAR-γ inhibition in 3T3-L1 adipocytes. Cytokine 2014; 69: 196-205.