Inhibition of autophagy augments chemotherapy in human salivary adenoid cystic carcinoma
作者
Jiang, LC;Huang, SY;Zhang, DS;Zhang, B;Li, KY;Li, WG;Zhang, SZ;Zhang, WD;Zheng, PH
作者单位
[Jiang, Licheng; Huang, Shengyun; Zhang, Dongsheng; Li, Wengang; Zhang, Shizhou; Zhang, Weidong; Zheng, Peihui] Shandong Univ, Dept Oral & Maxillofacial Surg, Prov Hosp, Jinan 250021, Peoples R China.;-;[Zhang, Bin; Li, Keyi] Liaocheng Peoples Hosp, Dept Oral & Maxillofacial Surg, Liaocheng, Peoples R China.
摘要
Although cisplatin (DDP)-based adjuvant chemotherapy is widely used in the treatment of salivary adenoid cystic carcinoma (SACC), SACCs have developed resistance to cisplatin, resulting in chemotherapy failure. Autophagy serves as a critical adaptive response, which was increased in tumor cells in chemotherapy. However, the function of autophagy is not clear in SACC. In this study, apoptosis induced by DDP in SACC high metastatic cell line (ACC-M) was revealed using MTT assay, flow cytometry, and caspase-3 immunoblotting. The autophagy activation induced by DDP treatment was measured by transmission electron microscopy, green fluorescent protein-light chain 3 plasmid transfection LC3 immunoblotting and p62 immunoblotting. 3-methyladenine (3-MA) or small interference RNA targeting beclin 1 (beclin 1 siRNA) inhibited autophagy and significantly enhanced DDP-induced apoptosis. ACC-M xenografts in nude mice further verified the synergistic effect of DDP and 3-MA. In conclusion, autophagy activation was caused to protect cancer cells from DDP-induced apoptosis and autophagy inhibition could be a promising strategy for adjuvant chemotherapy in SACC.
关键词
HUMAN CANCER-CELLS; INDUCED APOPTOSIS; GROWTH-CONTROL; P53; THERAPY; DEATH; PATHWAYS; SUPPRESSION; MECHANISMS; STRESS
基本信息
