Knockdown of RPL9 expression inhibits colorectal carcinoma growth via the inactivation of Id-1/NF-κB signaling axis

  • Authors:
    • In Hye Baik
    • Guk-Heui Jo
    • Daekwan Seo
    • Min Ji Ko
    • Chi Heum Cho
    • Min Goo Lee
    • Yun-Han Lee
  • View Affiliations

  • Published online on: September 13, 2016     https://doi.org/10.3892/ijo.2016.3688
  • Pages: 1953-1962
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Abstract

Ribosomal protein L9 (RPL9), a component of the 60S subunit for protein synthesis, is upregulated in human colorectal cancer. In the present study, we investigated whether RPL9 gained extraribosomal function during tumorigenesis and whether targeting of RPL9 with small interfering (si) RNA could alter the course of colorectal cancer progression. Our results showed that siRNA knockdown of RPL9 suppresses colorectal cancer (CRC) cell growth and long-term colony formation through an increase in sub-G1 cell population and a strong induction of apoptotic cell death. To obtain insights into the molecular changes in response to RPL9 knockdown, global changes in gene expression were examined using RNA sequencing. It revealed that RPL9-specific knockdown led to dysregulation of 918 genes in HCT116 and 3178 genes in HT29 cells. Among these, 296 genes showed same directional regulation (128 upregulated and 168 downregulated genes) and were considered as a common RPL9 knockdown signature. Particularly, we found through a network analysis that Id-1, which is functionally associated with activation of NF-κB and cell survival, was commonly downregulated. Subsequent western blot analysis affirmed that RPL9 silencing induced the decrease in the levels of Id-1 and phosphorylated IκBα in both HCT116 and HT29 cells. Also, the same condition decreased the levels of PARP-1 and pro-caspase-3, accelerating apoptosis. Furthermore, inhibition of RPL9 expression significantly suppressed the growth of human CRC xenografts in nude mice. These findings indicate that the function of RPL9 is correlated with Id-1/NF-κB signaling axis and suggest that targeting RPL9 could be an attractive option for molecular therapy of colorectal cancer.
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November-2016
Volume 49 Issue 5

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Baik IH, Jo G, Seo D, Ko MJ, Cho CH, Lee MG and Lee Y: Knockdown of RPL9 expression inhibits colorectal carcinoma growth via the inactivation of Id-1/NF-κB signaling axis. Int J Oncol 49: 1953-1962, 2016
APA
Baik, I.H., Jo, G., Seo, D., Ko, M.J., Cho, C.H., Lee, M.G., & Lee, Y. (2016). Knockdown of RPL9 expression inhibits colorectal carcinoma growth via the inactivation of Id-1/NF-κB signaling axis. International Journal of Oncology, 49, 1953-1962. https://doi.org/10.3892/ijo.2016.3688
MLA
Baik, I. H., Jo, G., Seo, D., Ko, M. J., Cho, C. H., Lee, M. G., Lee, Y."Knockdown of RPL9 expression inhibits colorectal carcinoma growth via the inactivation of Id-1/NF-κB signaling axis". International Journal of Oncology 49.5 (2016): 1953-1962.
Chicago
Baik, I. H., Jo, G., Seo, D., Ko, M. J., Cho, C. H., Lee, M. G., Lee, Y."Knockdown of RPL9 expression inhibits colorectal carcinoma growth via the inactivation of Id-1/NF-κB signaling axis". International Journal of Oncology 49, no. 5 (2016): 1953-1962. https://doi.org/10.3892/ijo.2016.3688