1.Expression and role of IL-33 and its receptor ST2 in eosinophilic and non-eosinophilic chronic rhinosinusitis with nasal polyps.
Tiancong LIU ; Changlong LV ; Zhiwei CAO
Journal of Clinical Otorhinolaryngology Head and Neck Surgery 2015;29(15):1350-1371
		                        		
		                        			OBJECTIVE:
		                        			To investigate the expression and role of Interleukin-33 (IL-33) and ST2 in the nasal polyps of human Eosinophilic and non-Eosinophilic chronic rhinosinusitis with nasal polyps (ECRS and non-ECRS).
		                        		
		                        			METHOD:
		                        			IL-33 and ST2 protein expression in nasal polyps of ECRS and non-ECRS as well as in seemingly normal mucosa of the inferior turbinate tissue was investigated by immunohistochemical staining and messenger RNA (mRNA) expression of IL-33 and ST2 was assessed by realtime polymerase chain reaction (PCR) in 27 subjects with ECRS, 33 subjects with non-ECRS, and 11 control subjects.
		                        		
		                        			RESULT:
		                        			(1) The ST2 was found both in nasal polyps of ECRS and non-ECRS,especially in ECRS, yet hardly found in the normal mucosa of the inferior turbinate tissue; (2) The expression of ST2 mRNA in nasal polyps of ECRS was higher than that in non-ECRS and normal inferior turbinate tissue, and the difference was both prominent in statistics (P<0.01); (3) The expression patterns of IL-33 at both mRNA and protein levels were not significantly different among the three groups (P>0.05).
		                        		
		                        			CONCLUSION
		                        			The IL-33 and its receptor ST2 were both expressed in human nasal polyps including ECRS and non-ECRS, meanwhile the expression patterns of ST2 at both mRNA and protein levels were significantly higher in nasal polyps of ECRS. The current study suggests that IL-33 and its receptor ST2 may play important roles in the pathogenesis of chronic rhinosinusitis with nasal polyps, especially in ECRS through the increased expression of ST2 in Eosinophils as a hypothesis.
		                        		
		                        		
		                        		
		                        			Chronic Disease
		                        			;
		                        		
		                        			Eosinophils
		                        			;
		                        		
		                        			immunology
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Interleukin-1 Receptor-Like 1 Protein
		                        			;
		                        		
		                        			Interleukin-33
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Nasal Mucosa
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Nasal Polyps
		                        			;
		                        		
		                        			immunology
		                        			;
		                        		
		                        			RNA, Messenger
		                        			;
		                        		
		                        			Real-Time Polymerase Chain Reaction
		                        			;
		                        		
		                        			Receptors, Cell Surface
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Rhinitis
		                        			;
		                        		
		                        			immunology
		                        			;
		                        		
		                        			Sinusitis
		                        			;
		                        		
		                        			immunology
		                        			;
		                        		
		                        			Turbinates
		                        			;
		                        		
		                        			metabolism
		                        			
		                        		
		                        	
2.Expression of galectin-7 and S100A9 and development of cervical squamous carcinoma.
Hong ZHU ; Li LIU ; Huan LIU ; Tiancong WU ; Yue WU ; Shan ZENG ; Liang ZENG
Journal of Central South University(Medical Sciences) 2013;38(9):888-895
		                        		
		                        			OBJECTIVE:
		                        			To observe the correlation between the expression of galectin-7 and S100A9 with the development of cervical squamous carcinoma.
		                        		
		                        			METHODS:
		                        			Immunohistochemical SP staining was used to detect the expression of galectin-7 and S100A9 in 243 patients with cervical intraepithelial neoplasia (CIN) or cervical squamous carcinoma. The association of clinical data with galectin-7 and S100A9 expression was examined.
		                        		
		                        			RESULTS:
		                        			The expression of galectin-7 and S100A9 in CIN and cervical squamous carcinoma was significantly different (P<0.05). The positive rates of galectin-7 in normal cervical tissues, CIN I, CIN II, CIN III, and cervical squamous carcinoma were 56.7%, 41.9%, 32.0%, 27.3%, and 25.0%, respectively. Statistic analysis found significant difference between the normal cervical tissues and cervical squamous carcinoma (P<0.0045). The positive rates of S100A9 in CIN I, CIN II, CIN III, and cervical squamous carcinoma were 80.0%, 77.4%, 48.0%, 27.3%, and 20.2%. Statistic analysis showed significant difference between the normal tissues and CIN III, the normal cervical tissues and cervical squamous carcinoma, CIN I and CIN III, CIN I and cervical squamous carcinoma, CIN II and cervical squamous carcinoma (P<0.0045). A positive correlation was found between galectin-7 and S100A9 expression in CIN and cervical squamous carcinoma (rs=0.298, P<0.001). Expressions of both galectin-7 and S100A9 in cervical squamous carcinoma were associated with the clinical stage and lymph nodes (P<0.05), but not with patient's age and degree of differentiation (P>0.05). Expression of galectin-7 was associated with the survival rate of patients with cervical squamous carcinoma (P<0.05). Univariate analysis of Cox proportional hazards regression model revealed that the FIGO stage, lymph nodes metastasis, and the expression of galectin-7 were relevant to the 5 year survival rate of patients with cervical squamous carcinoma, which was confirmed by multiple analysis of Cox proportional hazards regression model.
		                        		
		                        			CONCLUSION
		                        			Expression of galectin-7 and S100A9 is related with cervical the tumorigenesis of carcinoma, clinical stage, and lymph nodes of cervical squamous carcinoma. Galectin-7 is probably associated with the prognosis. The long-term survival of patients with cervical carcinoma may be associated with FIGO stage, lymph node metastasis, and the expression of galectin-7.
		                        		
		                        		
		                        		
		                        			Calgranulin B
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Carcinoma, Squamous Cell
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Cell Differentiation
		                        			;
		                        		
		                        			Cervical Intraepithelial Neoplasia
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Female
		                        			;
		                        		
		                        			Galectins
		                        			;
		                        		
		                        			metabolism
		                        			;
		                        		
		                        			Humans
		                        			;
		                        		
		                        			Lymphatic Metastasis
		                        			;
		                        		
		                        			Prognosis
		                        			;
		                        		
		                        			Proportional Hazards Models
		                        			;
		                        		
		                        			Survival Rate
		                        			;
		                        		
		                        			Uterine Cervical Neoplasms
		                        			;
		                        		
		                        			metabolism
		                        			
		                        		
		                        	
            
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