| Literature DB >> 27322737 |
Yun-Xin Lu1, Huai-Qiang Ju2, Feng Wang1, Le-Zong Chen1, Qi-Nian Wu1, Hui Sheng2, Hai-Yu Mo2, Zhi-Zhong Pan3, Dan Xie2, Tie-Bang Kang2, Gong Chen3, Jing-Ping Yun4, Zhao-Lei Zeng2, Rui-Hua Xu5.
Abstract
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.Entities:
Keywords: Chemoresistance; Colorectal cancer; Nafamostat mesilate; Nuclear factor kappa B; Oxaliplatin
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Year: 2016 PMID: 27322737 DOI: 10.1016/j.canlet.2016.06.014
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679