Zoledronic acid exhibits radio-sensitizing activity in human pancreatic cancer cells via inactivation of STAT3/NF-κB signaling

被引:5
作者
You, Yanjie [1 ]
Wang, Qiang [2 ]
Li, Haijun [3 ]
Ma, Yuhong [1 ]
Deng, Yanhong [1 ]
Ye, Zhengcai [4 ]
Bai, Feihu [1 ]
机构
[1] Ningxia Hui Autonomous Reg Peoples Hosp, Dept Gastroenterol, 301 Zhengyuan North Rd, Yinchuan 750021, Ningxia Hui Aut, Peoples R China
[2] Ningxia Hui Autonomous Reg Peoples Hosp, Dept Sci & Educ, 301 Zhengyuan North Rd, Yinchuan 750021, Ningxia Hui Aut, Peoples R China
[3] Second Peoples Hosp Neijiang, Dept Radiat Oncol, Neijiang 641003, Sichuan, Peoples R China
[4] Ningxia Hui Autonomous Reg Peoples Hosp, Endoscopy Ctr, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
pancreatic cancer; radio-resistance; zoledronic acid; radio-sensitizing effects; CARCINOMA-CELLS; TUMOR-GROWTH; RADIOSENSITIVITY; COMBINATION; BISPHOSPHONATES; ENHANCEMENT; INHIBITION; RADIATION; THERAPY;
D O I
10.2147/OTT.S202516
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Although pancreatic cancer is typically radio-sensitive, local treatment failure and metastasis are commonly caused by the development of resistance to radiotherapy. In the current study, the radio-sensitizing actions of zoledronic acid (ZOL) on pancreatic cancer cells were investigated. Materials and methods: Three human pancreatic cancer cell lines were exposed to ZOL, ionizing radiation (IR), or a combination of both, and the effects of the respective drug regimens on cell proliferation and invasion were examined. Results: Combined treatment with low doses of ZOL plus IR efficiently increased cell death and attenuated cell invasion compared with the individual use of ZOL or IR. These effects of ZOL were associated with inactivation of signal transducer and activator of transcription 3 (STAT3) and nuclear factor-kappa B (NF-kappa B). Conclusion: Collectively, these data suggest that ZOL in combination with IR is a promising therapeutic strategy for enhancing radio-sensitivity in pancreatic cancer cells via downregulation of the STAT3/NF-kappa B signaling pathway.
引用
收藏
页码:4323 / 4330
页数:8
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