Long-term defects of nasal epithelium barrier functions in patients with nasopharyngeal carcinoma post chemo-radiotherapy
Autor: | Hailing Chen, Zhenchao Zhu, Yang Peng, Jing Liu, Hongming Huang, Minghong Xu, Hsiao Hui Ong, Joshua K. Tay, Kai Sen Tan, De Yun Wang, Suizi Zhou, Junxiao Gao, Qianmin Chen, Qianhui Qiu |
---|---|
Rok vydání: | 2020 |
Předmět: |
Pathology
medicine.medical_specialty Inflammation 030218 nuclear medicine & medical imaging 03 medical and health sciences Basal (phylogenetics) 0302 clinical medicine Humans Medicine Radiology Nuclear Medicine and imaging Progenitor cell Nasopharyngeal Carcinoma business.industry Cell growth Epithelial Cells Nasopharyngeal Neoplasms Chemoradiotherapy Hematology medicine.disease Epithelium Nasal Mucosa medicine.anatomical_structure Oncology Nasopharyngeal carcinoma 030220 oncology & carcinogenesis Motile cilium Ultrastructure medicine.symptom business |
Zdroj: | Radiotherapy and Oncology. 148:116-125 |
ISSN: | 0167-8140 |
DOI: | 10.1016/j.radonc.2020.03.038 |
Popis: | Background and purpose Chronic and recurrent upper respiratory tract infection and inflammation is common in patients with nasopharyngeal carcinoma (NPC) post chemo-radiotherapy (CRT). Whether it is due to intrinsic (e.g., host-defense mechanisms of the epithelium), epigenetic or extrinsic factors is not fully understood. Materials and methods Tissue biopsies of the middle turbinate (MT) and inferior turbinate (IT) from NPC patients after CRT (mean of 3 years, n = 39) were compared with the IT biopsies from healthy subjects (n = 44). The epithelial ultrastructure was examined by transmission electron microscope (TEM). mRNA and protein expressions of epithelial stem/progenitor cells markers, as well markers of cell proliferation and differentiation markers was analyzed. Results Abnormal epithelial architecture was observed in all tissue samples of NPC patients. Significantly decreased expression levels of mRNA and protein levels for p63 (basal cells), Ki67 (cell proliferation), p63+/KRT5+ (epithelial stem/progenitor cells), MUC5AC and MUC5B (secretary proteins from goblet cells), alpha-tubulin, beta-tubulin and TAp73 (ciliated cells), DNAH5 and DNAI1 and RSPH4A (microtubule assemblies of motile cilia), FOXJ1 and CP110 (ciliogenesis-associated markers) were evident in MT and IT biopsies from NPC patients when compared to healthy controls. Conclusion CRT causes long-term defects of epithelial barrier functions and increases the susceptibility of these patients to upper respiratory tract infection and inflammation. |
Databáze: | OpenAIRE |
Externí odkaz: |