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Article

CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer

  • Authors:
    • Jin-Nyoung Ho
    • Jessie Sungyun Jeon
    • Dan Hyo Kim
    • Hoyoung Ryu
    • Sangchul Lee
  • View Affiliations / Copyright

    Affiliations: Department of Urology, Seoul National University, Bundang Hospital, Seongnam‑si, Gyeonggi‑do 13620, Republic of Korea, Department of Mechanical Engineering, KAIST, Daejeon 34141, Republic of Korea, Department of Urology, Ewha Womans University Medical Center, Seoul 07985, Republic of Korea
  • Article Number: 130
    |
    Published online on: May 8, 2023
       https://doi.org/10.3892/or.2023.8567
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Abstract

CUDC‑907 is a novel inhibitor of phosphoinositide 3‑kinase and histone deacetylase. It exerts anticancer activities by inducing apoptosis and inhibiting the growth and metastases of various tumors. However, the anticancer effects of CUDC‑907 on bladder cancer have not been previously reported. Thus, the present study aimed to examine the anticancer effects of CUDC‑907 on 2D monolayer and 3D spheroid models of T24 cells established from highly malignant human grade III urinary bladder carcinoma and cisplatin‑resistant T24R2 cells generated by 17 months of exposure to cisplatin, starting at 0.01 µg/ml and increasing stepwise to 2 µg/ml. CUDC‑907 treatment significantly reduced the cell viabilities of the monolayer and spheroid cultures in a concentration‑dependent manner. The IC50 value of CUDC‑907 was higher in the bladder cancer spheroids than in the monolayers. Treatment with CUDC‑907 suppressed epithelial‑mesenchymal transition via decreasing vimentin and E‑cadherin and consequently inhibited the migration and invasion of the bladder cancer spheroids. In addition, it promoted apoptosis and increased the expression of apoptosis‑related genes, such as Bax and caspases. In conclusion, CUDC‑907 exerted anticancer effects by reducing the viability, migration and invasion, and inducing apoptosis of bladder cancer spheroids. These results suggest that CUDC‑907 is a potent agent for the treatment of bladder cancer.
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Copy and paste a formatted citation
Spandidos Publications style
Ho J, Jeon JS, Kim DH, Ryu H and Lee S: CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer. Oncol Rep 49: 130, 2023.
APA
Ho, J., Jeon, J.S., Kim, D.H., Ryu, H., & Lee, S. (2023). CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer. Oncology Reports, 49, 130. https://doi.org/10.3892/or.2023.8567
MLA
Ho, J., Jeon, J. S., Kim, D. H., Ryu, H., Lee, S."CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer". Oncology Reports 49.6 (2023): 130.
Chicago
Ho, J., Jeon, J. S., Kim, D. H., Ryu, H., Lee, S."CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer". Oncology Reports 49, no. 6 (2023): 130. https://doi.org/10.3892/or.2023.8567
Copy and paste a formatted citation
x
Spandidos Publications style
Ho J, Jeon JS, Kim DH, Ryu H and Lee S: CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer. Oncol Rep 49: 130, 2023.
APA
Ho, J., Jeon, J.S., Kim, D.H., Ryu, H., & Lee, S. (2023). CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer. Oncology Reports, 49, 130. https://doi.org/10.3892/or.2023.8567
MLA
Ho, J., Jeon, J. S., Kim, D. H., Ryu, H., Lee, S."CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer". Oncology Reports 49.6 (2023): 130.
Chicago
Ho, J., Jeon, J. S., Kim, D. H., Ryu, H., Lee, S."CUDC‑907 suppresses epithelial‑mesenchymal transition, migration and invasion in a 3D spheroid model of bladder cancer". Oncology Reports 49, no. 6 (2023): 130. https://doi.org/10.3892/or.2023.8567
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