Aloperine Exerts Antitumor Effects on Bladder Cancer in vitro

Lijun Zhang1, Jun Liang1, Xiaohua Liu1

  • 1Department of Urology, Minda Hospital Affiliated to Hubei Minzu University, Enshi, Hubei Province, People's Republic of China.

Oncotargets and Therapy
|October 29, 2020
PubMed
Abstract

Insights

Aloperine (ALO) inhibits human bladder cancer cell proliferation and invasion while promoting apoptosis. This natural compound shows low toxicity to normal urothelial cells, indicating its potential as a bladder cancer therapeutic agent.

Area of Science:

  • Oncology
  • Natural Product Chemistry
  • Cell Biology

Background:

  • Human bladder cancer is a prevalent malignancy with limited effective therapies for advanced or recurrent cases.
  • Aloperine (ALO), a natural compound from Sophora alopecuroides, possesses known antitumor properties, but its specific role in bladder cancer was unexplored.

Purpose of the Study:

  • To investigate the efficacy and underlying mechanisms of Aloperine (ALO) in treating human bladder cancer.
  • To evaluate the cytotoxic effects of ALO on human bladder cancer cell lines and normal urothelial cells.

Main Methods:

  • Cytotoxicity was assessed using MTT assays on EJ (bladder cancer) and SV-HUC-1 (urothelial) cell lines.
  • Proliferation, apoptosis, migration, and invasion were analyzed using CCK-8, Hoechst staining, wound scratch, and Transwell assays.
  • Western blotting was employed to examine the expression of key proteins involved in cell signaling pathways.

Main Results:

  • Aloperine demonstrated significant inhibition of human bladder cancer EJ cell proliferation and invasion.
  • ALO treatment promoted apoptosis in cancer cells in vitro, mediated by Caspase activation.
  • ALO downregulated the protein expression of Ras, p-Raf1, and p-Erk1/2, suggesting pathway modulation.

Conclusions:

  • Aloperine exhibits promising therapeutic potential for human bladder cancer.
  • ALO shows selective toxicity towards cancer cells with low impact on normal urothelial cells.

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