Neutralization of matrix metalloproteinase-9 potentially enhances oncolytic efficacy of tanapox virus for melanoma therapy

被引:8
作者
Zhang, Tiantian [1 ]
Suryawanshi, Yogesh R. [1 ]
Szymczyna, Blair R. [2 ]
Essani, Karim [1 ]
机构
[1] Western Michigan Univ, Dept Biol Sci, Virol Lab, Kalamazoo, MI 49008 USA
[2] Western Michigan Univ, Dept Chem, Kalamazoo, MI 49008 USA
关键词
Tanapox virus; Metalloproteinase-9; Oncolytic virus; Melanoma; MATRIX METALLOPROTEINASES; GELATINASE-B; TUMOR-CELLS; IN-VITRO; EXPRESSION; INFECTION; NEUREGULIN; INHIBITORS; REGRESSION; CORRELATE;
D O I
10.1007/s12032-017-0988-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Matrix metalloproteinases (MMPs), which are involved in degradation of extracellular matrix, are critical regulators in tumor progression, metastasis and angiogenesis. Although induction of MMPs is frequently observed during the viral infection, the effect of MMPs on viral replication varies between viruses. MMP-9, for instance, is upregulated and promotes the replication of some viruses, such as herpes simplex virus, but inhibits the replication of others. Here, we report that infection with tanapox virus (TPV) promotes the expression of MMP-9 in the melanoma cells. In addition, we show that MMP-9 exerts an anti-viral effect on TPV replication and plays a protective role in TPV-infected melanoma cells in vitro. Moreover, the neutralization of MMP-9 in melanoma cells remarkably enhances the TPV infection and leads to a significant reduction in cell survival. In summary, this study contributes to understanding of the role played by MMP-9 in TPV infectivity and provides more insights for using TPV as cancer virotherapy in future studies. Since TPV has shown substantial oncolytic efficacy in promoting melanoma tumor regression in animal models, identifying mechanisms that suppress MMP-9 expression upon TPV infection can potentially improve its use as a melanoma virotherapy.
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页数:11
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