The PAD4 inhibitor GSK484 enhances the radiosensitivity of triple-negative breast cancer

被引:23
作者
Wei, Lining [1 ]
Wang, Xiangping [2 ]
Luo, Min [2 ]
Wang, Hongzhi [2 ]
Chen, Hao [2 ]
Huang, Changjie [2 ]
机构
[1] Guangxi Med Univ, Dept Endoscopy, Affiliated Tumor Hosp, Nanning, Guangxi, Peoples R China
[2] Second Nanning Peoples Hosp, Dept Oncol, 13 Dancun Rd, Nanning, Guangxi, Peoples R China
关键词
GSK484; radiosensitivity; autophagy; triple-negative breast cancer; TARGETING AUTOPHAGY; RADIOTHERAPY; METASTASIS;
D O I
10.1177/0960327120979028
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Triple-negative breast cancer (TNBC) accounts for approximately 10-20% of all breast cancers and is one of the leading causes of mortality among females. Radiotherapy is essential during the treatment of breast cancer. Growing evidence has indicated that peptidyl arginine deiminase-4 (PAD4) inhibitor can alleviate the development of multiple cancers, including breast cancer, through inhibiting cell proliferation. GSK484 is considered to be a highly potent PAD4-selective inhibitors. However, the potential role and mechanism of GSK484 in TNBC remain unclear. In this study, we intended to explore the effects of GSK484 on the radiosensitivity of TNBC cell lines (MDA-MB-231 and BT-549). We found that the pretreatment of GSK484 enhanced irradiation (IR)-induced inhibitory effects on cell proliferation, migration and invasion. Besides, our findings revealed that GSK484 facilitated TNBC cell apoptosis. IR treatment-induced increase of the protein level of ATG5 and ATG7, and decrease of p62 protein level were countervailed by GSK484. In addition, GSK484 enhanced DNA damage induced by IR. Moreover, in vivo experiments demonstrated that the combined treatment of IR and GSK484 showed an obvious decline of tumor growth in contrast to IR-alone or GSK484-alone treatment. Overall, GSK484 may serve as a radiosensitizer of TNBC through inhibiting IR-induced autophagy.
引用
收藏
页码:1074 / 1083
页数:10
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