Inhibition of the NF-κB pathway by nafamostat mesilate suppresses colorectal cancer growth and metastasis

被引:55
|
作者
Lu, Yun-Xin [1 ,2 ]
Ju, Huai-Qiang [1 ]
Wang, Feng [1 ,2 ]
Chen, Le-Zong [1 ,2 ]
Wu, Qi-Nian [1 ,2 ]
Sheng, Hui [1 ]
Mo, Hai-Yu [1 ]
Pan, Zhi-Zhong [1 ,3 ]
Xie, Dan [1 ]
Kang, Tie-Bang [1 ]
Chen, Gong [1 ,3 ]
Yun, Jing-Ping [1 ,4 ]
Zeng, Zhao-Lei [1 ]
Xu, Rui-Hua [1 ,2 ]
机构
[1] Sun Yat Sen Univ, Ctr Canc, State Key Lab Oncol South China, Collaborat Innovat Ctr Canc Med, Guangzhou 510060, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Ctr Canc, Dept Med Oncol, Guangzhou, Guangdong, Peoples R China
[3] Sun Yat Sen Univ, Ctr Canc, Dept Colorectal Surg, Guangzhou, Guangdong, Peoples R China
[4] Sun Yat Sen Univ, Ctr Canc, Dept Pathol, Guangzhou, Guangdong, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划); 中国博士后科学基金;
关键词
Nafamostat mesilate; Colorectal cancer; Chemoresistance; Nuclear factor kappa B; Oxaliplatin; PERITONEAL DISSEMINATION; COMBINATION CHEMOTHERAPY; CELL-LINES; OXALIPLATIN; ACTIVATION; RESISTANCE; GEMCITABINE; IDENTIFICATION; FLUOROURACIL; LEUCOVORIN;
D O I
10.1016/j.canlet.2016.06.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Nafamostat mesilate is an anti-inflammatory drug that is usually used to treat pancreatitis. Recent studies show that it can suppress pancreatic cancer via inhibition of the nuclear factor kappa B (NF-kappa B) pathway. However, whether it has anti-tumor activity in some other cancer, including colorectal cancer (CRC), has not been investigated and remained unclear. Here, our study showed that nafamostat mesilate abrogated the constitutive NF-kappa B activation in CRC cells, which is mediated through inhibition of phosphorylation of I kappa B alpha and nuclear translocation of p65. Also, we found that nafamostat mesilate inhibited phosphorylation of Erk in CRC cells. Consistently, our study demonstrated that nafamostat mesilate inhibited the CRC cell proliferation, invasion and migration and induced mitochondria-dependent apoptosis. Furthermore, nafamostat mesilate could reverse oxaliplatin induced NF-kappa B and Erk activation in CRC cells, and enhance the sensitivity of CRC cells to oxaliplatin. Nafamostat mesilate combined with oxaliplatin repressed subcutaneous tumor growth and hepatic metastasis in vivo. Overall, our data suggest that nafamostat mesilate, a relatively non-toxic drug that targets NF-kappa B and Erk, may, in combination with oxaliplatin, represent a novel therapeutic strategy for CRC treatment. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:87 / 97
页数:11
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