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Related Concept Videos

The Intrinsic Apoptotic Pathway01:31

The Intrinsic Apoptotic Pathway

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Internal cellular stress, such as cellular injury or hypoxia, triggers intrinsic apoptosis. The B-cell lymphoma 2 (Bcl-2) family of proteins are the primary regulators of the intrinsic apoptotic pathway. For example, during DNA damage, checkpoint proteins, such as Ataxia Telangiectasia Mutated (ATM protein) and Checkpoints Factor-2 (Chk2) proteins, are activated. These proteins phosphorylate p53 which further activates pro-apoptotic proteins, such as Bax, Bak, PUMA, and Noxa, and inhibits...
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Protective Role of Protocatechuic Acid in Glioma: Modulation of Cell Growth, Migration, and Pyroptosis via

Wen Zhang1, Yeyan Cai1, Haijun Zheng1

  • 1Department of Neurosurgery, The Third Affiliated Hospital of Wenzhou Medical University, 325200 Wenzhou, Zhejiang, China.

Discovery Medicine
|April 27, 2025
PubMed
Summary

Protocatechuic acid (PCA) triggers pyroptosis in glioma cells, inhibiting their growth and spread. This natural compound activates the NLRP3/caspase-1/GSDMD pathway, offering a potential new avenue for glioblastoma treatment.

Keywords:
NLRP3/caspase-1/GSDMD pathwayU251U87glioma cellsprotocatechuic acidpyroptosis

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Area of Science:

  • Oncology
  • Molecular Biology
  • Natural Products Chemistry

Background:

  • Glioblastoma is a deadly brain tumor with limited treatment options.
  • Protocatechuic acid (PCA), a natural phenolic compound, exhibits promising anti-tumor properties.
  • Understanding PCA's mechanism in glioma is crucial for developing new therapies.

Purpose of the Study:

  • To investigate if PCA can induce pyroptosis in glioma cells.
  • To elucidate the specific molecular pathways involved in PCA's anti-glioma effects.
  • To assess PCA's impact on glioma cell viability, invasion, and migration.

Main Methods:

  • Glioma cells (U87, U251) were treated with varying PCA concentrations.
  • Cell proliferation, invasion, and migration were assessed using CCK-8, Transwell, and scratch assays.
  • Pyroptosis, NLRP3, caspase-1, and GSDMD expression were analyzed via immunofluorescence, Western blotting, and qRT-PCR.

Main Results:

  • PCA significantly reduced glioma cell viability, invasion, and migration in a dose-dependent manner.
  • PCA treatment increased pyroptosis markers and the expression of NLRP3, caspase-1, and GSDMD.
  • Inhibition of NLRP3 by MCC950 reversed PCA's effects, confirming pathway involvement.

Conclusions:

  • PCA effectively induces pyroptosis in glioma cells.
  • The NLRP3/caspase-1/GSDMD signaling pathway is critical for PCA's anti-glioma activity.
  • PCA represents a potential therapeutic agent for glioblastoma.