奥沙利铂
结直肠癌
癌症研究
MAPK/ERK通路
转移
胰腺癌
细胞凋亡
医学
癌症
药理学
激酶
化学
内科学
生物化学
作者
Yun Lü,Huai‐Qiang Ju,Feng Wang,Le Zong Chen,Qi Wu,Hui Sheng,Hai Yu Mo,Zhi Zhong Pan,Dan Xie,Tie Bang Kang,Gong Chen,Jing Ping Yun,Zhao Lei Zeng,Rui‐Hua Xu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2016-09-01
卷期号:380 (1): 87-97
被引量:52
标识
DOI:10.1016/j.canlet.2016.06.014
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 κB (NF-κB) 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-κB activation in CRC cells, which is mediated through inhibition of phosphorylation of IκBα 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-κB 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-κB and Erk, may, in combination with oxaliplatin, represent a novel therapeutic strategy for CRC treatment.
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