1. PO-382 Evaluation of the serum level of T-helper-17 in patients with benign and malignant salivary gland tumours
- Author
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Behzad Khademi, Mahyar Malekzadeh, M. Hashemi, and Razieh Zare
- Subjects
Cancer Research ,Pathology ,medicine.medical_specialty ,Salivary gland ,business.industry ,Adenoid cystic carcinoma ,medicine.disease ,medicine.disease_cause ,Pleomorphic adenoma ,medicine.anatomical_structure ,Oncology ,Mucoepidermoid carcinoma ,medicine ,Interleukin 23 ,Biomarker (medicine) ,IL17A ,business ,Carcinogenesis - Abstract
Introduction Salivary gland tumours (SGTs) are important parts of human neoplasms. The most common SGT is the pleomorphic adenoma (PA); and the most common malignant SGTs are mucoepidermoid carcinoma (MEC) and adenoid cystic carcinoma(ADCC). T-helper-17 cells (Th17) are characterised with the ability to secrete cytokines including IL17A, IL17F, IL9, IL21, IL22, IL23, IL26 and TNF-α. Th17 cells play important role in inflammatory disease, infections, and cancers. This study aimed to investigate the role of Th17 in sera level of patients with SGTs. Material and methods The level of IL9,TNF-α, IL17A,IL17F, and IL21 were measured in the sera of 43 patients with malignant SGTs, 28 patients with benign SGTs, and 4 patients with inflammation in comparison with 25 healthy controls by using flow cytometry assays. The data were analysed by using Kruskal-Wallis and Mann-Whitney tests. Results and discussions The findings revealed the IL17A to have increased in SGTs compared with the healthy controls (p=0.009 and p=0.002, respectively). The serum level of IL17A increased significantly in MEC, ADCC and PA tumour types compare with the control group (p=0.001, p=0.050, p=0.002, respectively). There was no significant differen with other Th17 cytokines and groups with clinicopathological parameters. Conclusion The results showed that IL17A was significantly overexpressed in malignant and benign SGTs, suggesting that IL17A might be involved in carcinogenesis. It was concluded that IL17A could be a novel biomarker for distinguishing different malignant SGTs.
- Published
- 2018
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