Timosaponin AIII inhibits metastasis of renal carcinoma cells through suppressing cathepsin C expression by AKT/miR-129-5p axis

被引:40
|
作者
Chiang, Kuang-Chung [1 ]
Lai, Chung-Yu [2 ,3 ]
Chiou, Hui-Ling [4 ]
Lin, Chia-Liang [5 ]
Chen, Yong-Syuan [5 ]
Kao, Shao-Hsuan [5 ,6 ]
Hsieh, Yi-Hsien [5 ,6 ,7 ]
机构
[1] Cheng Ching Gen Hosp, Chung Kang Branch, Dept Urol, Taichung, Taiwan
[2] Chung Shan Med Univ, Inst Med, Taichung, Taiwan
[3] Cheng Ching Gen Hosp, Chung Kang Branch, Dept Thorac Surg, Taichung, Taiwan
[4] Chung Shan Med Univ, Sch Med Lab & Biotechnol, Taichung, Taiwan
[5] Chung Shan Med Univ, Inst Biochem Microbiol & Immunol, 110,Sect 1,Chien Kuo N Rd, Taichung, Taiwan
[6] Chung Shan Med Univ Hosp, Clin Lab, Taichung, Taiwan
[7] Chung Shan Med Univ, Sch Med, Dept Biochem, Taichung, Taiwan
关键词
cathepsin C; invasion; migration; renal cell carcinoma; timosaponin AIII (TSAIII); CANCER CELLS; INVASION; GROWTH; APOPTOSIS; MIGRATION; DYSFUNCTION;
D O I
10.1002/jcp.28010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Timosaponin AIII (TSAIII) is a steroidal saponin that exerts anticancer activity on various cancer cells. In this study, we explore the effects of TSAIII on renal cell carcinoma (RCC) cells. Our findings show that TSAIII treatment (<8 M) insignificantly influenced cell viability and cell cycle distribution of human RCC cell lines 786-O, A-498, and ACHN. Further observations revealed that TSAIII inhibited migration and invasion of 786-O and A-498 cells, as well as significantly decreased the production and expression of cathepsin C (CTSC) in both the cell types. Kinase cascade analysis exhibited that PI3K/AKT activation was inhibited, but PTEN expression was increased, in response to TSAIII treatments. Combining TSAIII and PI3K inhibitors, LY294002 synergically reduced the migration and invasion of 786-O and A-498 cells, as well as decreased the CTSC expression in both the cell types. We also observed that miR-129-5p bound to CTSC gene and suppressed the expression of CTSC and demonstrated that the miR-129-5p expression was synergically enhanced by TSAIII and LY294002. In addition, pretreatment with antago-miR-129-5p significantly restored the CTSC expression and the migration and invasion of TSAIII-treated 786-O cells. In conclusion, our findings reveal that TSAIII inhibits the metastatic properties of RCC cells, contributing to the inhibition of PI3K/AKT and the increase of miR-129-5p and the subsequent downregulation of CTSC. This suggests that TSAIII has significant antimetastatic activity against RCC cells and may be beneficial to RCC treatments.
引用
收藏
页码:13332 / 13341
页数:10
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