| Autor: |
Huang ZH; Department of Head & Neck Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Science and Peking Union Medical College , Beijing, P.R. China., Qiao J; Department of Rheumatology, The Second Hospital of Shanxi Medical University , Taiyuan, P.R. China., Feng YY; Shanxi Medical University , Taiyuan, P.R. China., Qiu MT; Department of Rheumatology, The Second Hospital of Shanxi Medical University , Taiyuan, P.R. China., Cheng T; Department of Rheumatology, The Second Hospital of Shanxi Medical University , Taiyuan, P.R. China., Wang J; Department of Rheumatology, The Second Hospital of Shanxi Medical University , Taiyuan, P.R. China., Zheng CF; Linfen Meternity & Child Healthcare Hospital , Linfen, P.R. China., Lv ZQ; Department of Rheumatology, The Second Hospital of Shanxi Medical University , Taiyuan, P.R. China., Wang CH; Department of Rheumatology, The Second Hospital of Shanxi Medical University , Taiyuan, P.R. China. |
| Abstrakt: |
Nasopharyngeal carcinoma (NPC) mainly appears in southeastern Asian countries, including China. Adriamycin (ADM), a type of antitumor drug, is widely applied in treatments against various cancers. Nevertheless, cancer cells will eventually develop drug resistance to ADM. The present study aims to explore the potential role of reticulocalbin-1 (RCN1) in NPC cells resistance to ADM. Microarray-based analysis was used to screen NPC-related genes, with RCN1 acquired for this current study. RCN1 expression in NPC tissues and cells was determined. The biological function of RCN1 on NPC cell apoptosis was evaluated via gain- and loss-of-function experiments in 5-8 F/ADM and 5-8 F cells by delivering si-RCN1 and RCN1-vector. The function of endoplasmic reticulum (ER) stress on cell apoptosis was measured with the involvement of the PERK-CHOP signaling pathway. Furthermore, tumor formation in nude mice was performed to evaluate the survival condition and RCN1 effects in vivo . RCN1 was highly expressed in NPC tissues and cell lines. The increased expression of ER-related proteins ATF4, CHOP, and the extents of IRE1 and PERK phosphorylation were observed. RCN1 knockdown was found to reduce resistance of NPC cells/tissues to ADM while activating ER stress through the activated PERK-CHOP signaling pathway, which further promoted NPC cell apoptosis. These in vitro findings were detected in vivo on tumor formation in nude mice. In conclusion, the present study provides evidence that RCN1 knockdown stimulates ADM sensitivity in NPC by promoting ER stress-induced cell apoptosis, highlighting a theoretical basis for NPC treatment. |
