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Targeted Silencing of Kim-1 Inhibits the Growth of Clear Cell Renal Cell Carcinoma Cell Line 786-0 In Vitro and In Vivo

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Department of Urology, Tumor Hospital of Linyi City, Lanshan, Linyi, Shandong, P.R. China

Oncology Research 2018, 26(7), 997-1003. https://doi.org/10.3727/096504017X15140544654946

Abstract

To investigate the effect of Kim-1 on 786-0 cells in vivo and in vitro, several experiments such as quantitative real-time PCR, Western blot, MTT, colony formation, and flow cytometry were performed to evaluate the biological behavior of 786-0 cells treated with Kim-1 siRNA. Furthermore, the tumor xenograft model was applied to BALB/c nude mice to assess the effect of Kim-1 silencing. Lentivirus-mediated RNAi effectively silenced Kim-1 in 786-0 cells. Kim-1 knockdown significantly inhibited the proliferation and colony formation ability of 786-0 cells (p < 0.01). The cell cycle of 786-0 cells was arrested in the G0/G1 phase (p < 0.01). Early and late apoptosis were significantly increased in the Kim-1 siRNA cells (p < 0.01). In addition, growth of 786-0 cells was significantly inhibited in the Kim-1-silenced mice. In conclusion, knockdown of Kim-1 inhibits the growth of 786-0 cells in vitro and in vivo, indicating that Kim-1 could be used as a potential target for clear cell renal cell carcinoma therapy.

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APA Style
Xu, J., Sun, L., Sun, W., Tian, J., Guo, H. (2018). Targeted silencing of kim-1 inhibits the growth of clear cell renal cell carcinoma cell line 786-0 in vitro and in vivo. Oncology Research, 26(7), 997-1003. https://doi.org/10.3727/096504017X15140544654946
Vancouver Style
Xu J, Sun L, Sun W, Tian J, Guo H. Targeted silencing of kim-1 inhibits the growth of clear cell renal cell carcinoma cell line 786-0 in vitro and in vivo. Oncol Res. 2018;26(7):997-1003 https://doi.org/10.3727/096504017X15140544654946
IEEE Style
J. Xu, L. Sun, W. Sun, J. Tian, and H. Guo, “Targeted Silencing of Kim-1 Inhibits the Growth of Clear Cell Renal Cell Carcinoma Cell Line 786-0 In Vitro and In Vivo,” Oncol. Res., vol. 26, no. 7, pp. 997-1003, 2018. https://doi.org/10.3727/096504017X15140544654946



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