2. Academic Validation
  3. Sakuranin represses the malignant biological behaviors of human bladder cancer cells by triggering autophagy via activating the p53/mTOR pathway

Sakuranin represses the malignant biological behaviors of human bladder cancer cells by triggering autophagy via activating the p53/mTOR pathway

  • BMC Urol. 2023 Oct 24;23(1):170. doi: 10.1186/s12894-023-01334-2.
Ling Hao 1,  Dandan Mu 2,  Haitao Mu 3
Affiliations

Affiliations

  • 1 Department of Medical Oncology, The Fourth Affiliated Hospital of Harbin Medical University, No.37, Yiyuan Street, Harbin, 150000, China. [email protected].
  • 2 Department of Medical Oncology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
  • 3 Department of Medical Oncology, The Fifth Hospital of Harbin, Harbin, China.
PMID: 37875863 DOI: 10.1186/s12894-023-01334-2
Abstract

Objective: Sakura extract is a natural flavonoid compound that may have potential anti-tumor effects. The paper focuses on investigating Sakuranin mechanism on bladder Cancer (BC) cells.

Methods: BC cells (T24) were treated with different concentrations of Sakuranin, with 48-h IC50 determined. T24 cells were treated with Sakuranin at IC50, followed by assessment of cell proliferative/apoptotic/migrative/invasive activities by CCK-8, EdU and plate clone formation assays/flow cytometry/Transwell/scratch test. MMP-2 (migration and invasion-related protein) protein level was assessed by Western blot. Cell Autophagy was evaluated by measuring the protein levels of Autophagy markers (LC3-I/LC3-II/p62) through Western blot. The Autophagy Inhibitor 3-MA was used to validate the role of Autophagy in the regulatory mechanism of Sakuranin in T24 cell behaviors. Furthermore, the activation of the p53/mTOR pathway in cells was detected and a combination of Sakuranin and p53 inhibitor Pifithrin-µ was adopted to explore the involvement of this pathway.

Results: Sakuranin decreased T24 cell proliferation/EdU positive cell percentage/colony formation number and area/migration/invasion/scratch healing/MMP-2 protein level, and accelerated Apoptosis. Sakuranin elevated the LC3-II/I ratio and lowered p62 level in T24 cells. 3-MA partially averted Sakuranin-mediated repression on cell malignant behaviors. Sakuranin upregulated p-p53 and p53 levels, and decreased the p-mTOR/mTOR ratio in T24 cells. The effects of Sakuranin on cell biological behaviors were partly annulled by Pifithrin-µ treatment.

Conclusion: Sakuranin suppressed T24 cell proliferation/migration/invasion, and enhanced Apoptosis by potentiating Autophagy through activating the p53/mTOR pathway. This study provided a theoretical basis for Sakuranin as a potential drug for clinical treatment of BC.

Keywords

Apoptosis; Autophagy; Bladder cancer; Proliferation; Sakuranin; T24 cells; p53/mTOR pathway.

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