| Literature DB >> 27693494 |
Yijie Chen1, Yang Yu1, Shuya Sun1, Zhaotong Wang2, Peiqing Liu3, Shenglan Liu1, Jianmin Jiang4.
Abstract
Tumor metastasis is the main reason of death for hepatocellular carcinoma (HCC) patients. Cell migration and invasion are two prerequisites for tumor metastasis, in which TRPM7 and MMPs play an important role. In our study, we found that bradykinin (BK) could upregulate the expression of TRPM7 and dynamically regulate the phosphorylation of non-muscle myosin IIA heavy chain (NMHC-IIA) Ser-1943 in HepG2 cells. The influx of Ca2+ via TRPM7 was necessary for elevating the activity of m-calpain and μ-calpain. Additionally, we observed that BK stimulated HepG2 cells to secrete more MMP2 but not MMP9. Src was critical in the process of MMP2 secretion and invadopodia formation. The heat map showed that BDKRB2, TRPM7 and MMP2 had higher overexpression proportions in 25 HCC cell lines. Some clinical specimens of HCC also indicated that BDKRB2 and MMP2 were overexpressed. In conclusion, BK promoted migration and invasion of HCC cells through TRPM7 and MMP2.Entities:
Keywords: Bradykinin; Invasion; MMP2; Migration; TRPM7
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Year: 2016 PMID: 27693494 DOI: 10.1016/j.yexcr.2016.09.022
Source DB: PubMed Journal: Exp Cell Res ISSN: 0014-4827 Impact factor: 3.905