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786-0 Renal cancer cell line-derived exosomes promote 786-0 cell migration and invasion in vitro

机译:786-0肾癌细胞系外泌体在体外促进786-0细胞迁移和侵袭

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摘要

Emerging evidence indicates that cancer-derived exosomes contribute to angiogenesis, tumor immunology and invasion. However, whether cancer cell-derived exosomes regulate the migration and invasion of the cancer cell itself, and the underlying mechanisms are not well understood. In the present study, exosomes derived from the 786-0 human renal cancer cell line were isolated, purified and 100 μg/ml were co-cultured with 786-0 cells for 24 h. The 786-0 cells were harvested for a cell invasion and migration assay. The expression of chemokine receptor type 4 (CXCR4) and matrix metalloproteinase-9 (MMP-9) in the 786-0 cells was examined by western blot analysis and revealed that the migration and invasion capabilities of the 786-0 cells were increased, however, the cell adhesion abilities were decreased as a result of the 24-h treatment with 786-0-derived exosomes. Furthermore, the expression levels of CXCR4 and MMP-9 in the 786-0 cells were increased. In conclusion, the 786-0 renal cancer cell line-derived exosomes increased migration and invasion, however, they decreased the adhesion ability of the 786-0 cells. The exosomes may have increased the CXCR4 and MMP-9 expression levels in the 786-0 cells. These findings indicated that renal tumor-derived exosomes may contribute to renal cancer development and progression.
机译:越来越多的证据表明,癌症来源的外来体有助于血管生成,肿瘤免疫学和侵袭。但是,癌细胞衍生的外来体是否调节癌细胞本身的迁移和侵袭,其潜在机制尚不清楚。在本研究中,分离,纯化了源自786-0人肾癌细胞系的外泌体,并将100μg/ ml与786-0细胞共培养24小时。收获786-0细胞用于细胞侵袭和迁移测定。通过western印迹分析检查了786-0细胞中趋化因子受体4型(CXCR4)和基质金属蛋白酶9(MMP-9)的表达,发现其增加了786-0细胞的迁移和侵袭能力,但是,使用786-0衍生的外泌体进行24小时治疗后,细胞粘附能力下降。此外,CXCR4和MMP-9在786-0细胞中的表达水平增加。总之,源自786-0肾癌细胞系的外泌体增加了迁移和侵袭,但是,它们降低了786-0细胞的粘附能力。外泌体可能已经增加了786-0细胞中的CXCR4和MMP-9表达水平。这些发现表明,肾肿瘤来源的外来体可能有助于肾癌的发生和发展。

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