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Cancer treatment vaccines are a rapidly evolving field that offers a promising approach to immunotherapy. Unlike traditional vaccines that prevent diseases, cancer treatment vaccines are designed to treat existing cancers by stimulating the immune system to recognize and attack cancer cells.
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The mammalian target of rapamycin or mTOR protein was discovered in 1994 due to its direct interaction with rapamycin. The protein gets its name from a yeast homolog called TOR. The mTOR protein complex in mammalian cells plays a major role in balancing anabolic processes such as the synthesis of proteins, lipids, and nucleotides and catabolic processes, such as autophagy in response to environmental cues, such as availability of nutrients and growth factors.
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Related Experiment Video

Updated: Jul 16, 2025

Author Spotlight: Exploring Salidroside's Molecular Mechanisms in Breast Cancer Treatment
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Cannabidiol Inhibits the Proliferation and Invasiveness of Prostate Cancer Cells.

Eve O'Reilly1,2, Karima Khalifa1,2, Joanne Cosgrave1,2

  • 1UCD School of Biology and Environmental Science, University College Dublin, Dublin D04 C1P1, Ireland.

Journal of Natural Products
|September 13, 2023
PubMed
Summary

Cannabidiol (CBD) shows promise in fighting prostate cancer by inhibiting cell growth and invasion. This study suggests CBD may be a potential future chemotherapeutic agent for prostate cancer treatment.

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Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Prostate cancer is a leading cause of cancer death in men.
  • Novel therapeutic strategies are urgently needed to improve patient outcomes.
  • Cannabinoids, derived from cannabis, show preclinical potential against various cancers.

Purpose of the Study:

  • To investigate the antiproliferative and anti-invasive effects of cannabidiol (CBD) on prostate cancer cells in vitro.
  • To explore the molecular mechanisms underlying CBD's action in prostate cancer.

Main Methods:

  • Prostate cancer cell lines were treated with CBD.
  • Cell viability, proliferation, cell cycle protein expression, AKT phosphorylation, and cell invasiveness were assessed.
  • Experiments included the use of cannabinoid receptor antagonists and TRPV1/GPR55 modulators.

Main Results:

  • CBD significantly inhibited prostate cancer cell viability and proliferation.
  • CBD reduced the expression of cell cycle proteins (cyclin D3, CDK2, CDK4, CDK1) and AKT phosphorylation.
  • CBD decreased PC-3 cell invasiveness and increased E-cadherin expression, independent of known cannabinoid targets.

Conclusions:

  • CBD exhibits significant antiproliferative and anti-invasive properties in prostate cancer cells.
  • CBD's mechanism of action appears independent of cannabinoid receptors, TRPV1, and GPR55.
  • CBD demonstrates potential as a novel chemotherapeutic agent for prostate cancer.