Cytochalasin D promotes pulmonary metastasis of B16 melanoma through expression of tissue factor
文献类型: 外文期刊
作者: Huang, Feng-Ying 1 ; Mei, Wen-Li 2 ; Tan, Guang-Hong 1 ; Dai, Hao-Fu 2 ; Li, Yue-Nan 1 ; Guo, Jun-Li 1 ; Huang, Yong-H 1 ;
作者机构: 1.Hainan Med Coll, Hainan Prov Key Lab Trop Med, Haikou 571101, Hainan, Peoples R China
2.Chinese Acad Trop Agr Sci, Inst Trop Biosci & Biotechnol, Haikou, Hainan, Peoples R China
关键词: Clotting factor factor VII;Cytochalasin D;Mitogen-activated protein kinase p38;Tissue factor;Tumor metastasis
期刊名称:ONCOLOGY REPORTS ( 影响因子:3.906; 五年影响因子:4.011 )
ISSN:
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收录情况: SCI
摘要: Cytochalasin D (CytD) targets actin, a ubiquitous protein in eukaryotic cells. Previous studies have focused mainly on the antitumor effects of CytD. We previously found CytD to promote lung metastasis in B16 melanoma cells, which we had not anticipated, and, therefore, in the present study we investigated the possible underlying mechanisms. B16 melanoma cells were co-cultured with CytD and other agents and used to establish a lung metastatic model. In this B16 melanoma metastatic model, significantly increased lung metastasis and lung weight were found in CytD-treated mice, which was almost completely suppressed by tissue factor (TF) RNA interference expressed via lentivirus. The results of northern and western blot, and real-time RT-PCR analysis showed that the expression of TF was significantly upregulated in B16 cells treated with CytD but was significantly inhibited by TF RNA interference. In addition, upregulation and phosphorylation of mitogen-activated protein kinase p38 were also found in the metastatic lung tissues treated with CytD and in the B16 cells co-cultured with CytD and factor VIIa (FVIIa), but not in cells cultured with CytD, dimethyl sulfoxide or FVIIa alone. These results indicate that CytD stimulates the expression of TF in B16 melanoma cells, activating both coagulation-dependent and -independent pathways via binding to FVIIa, eventually promoting lung metastasis. TF interference is a potential approach to the prevention of B16 melanoma metastasis.
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