Unravelling the antitumor mechanism of Ocoxin through cancer cell genomics

Iera Hernandez-Unzueta1, Uxue Telleria-Gonzalez1, Ana María Aransay2,3

  • 1Cell Biology and Histology Department, Faculty of Medicine and Nursing, University of the Basque Country, Leioa, Spain.

PubMed

Insights

Ocoxin, a natural compound, shows potential as an adjunctive cancer treatment by altering cell metabolism and inducing cell death pathways like ferroptosis. This study investigated its mechanisms in colorectal, breast, pancreatic, and prostate cancers.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Cancer remains a leading global cause of death, with existing therapies often limited by efficacy and severe side effects impacting patient quality of life.
  • Ocoxin, a complex mixture of plant extracts, amino acids, vitamins, and minerals, possesses known antioxidant, anti-inflammatory, and immunoregulatory properties.
  • Preclinical studies suggest Ocoxin exhibits antitumor effects across various cancer types.

Purpose of the Study:

  • To elucidate the specific mechanisms of action of Ocoxin in four distinct cancer models: colorectal cancer, triple-negative breast cancer, pancreatic cancer, and prostate cancer.
  • To identify common and cancer-specific molecular pathways modulated by Ocoxin.
  • To evaluate the potential of Ocoxin as an adjunctive therapeutic agent.

Main Methods:

  • RNA sequencing was employed to analyze gene expression changes induced by Ocoxin in the selected cancer models.
  • Bioinformatic analyses were performed to identify key biological pathways affected by Ocoxin treatment.
  • Comparative analysis across different cancer types was conducted to find common molecular targets.

Main Results:

  • Ocoxin primarily alters cancer cell metabolism, notably inducing ferroptosis, a regulated form of cell death.
  • Significant modulation of the cell cycle was observed, indicating interference with cancer cell proliferation.
  • Ocoxin affected 13 common genes across all four cancer types, implicating metabolism, cell cycle, integrated stress response, and unfolded protein response pathways in its mechanism of action.

Conclusions:

  • Ocoxin induces cancer cell death through multiple pathways, including ferroptosis, cell cycle modulation, integrated stress response, and unfolded protein response.
  • While specific mechanisms vary by cancer type, Ocoxin demonstrates potential as a complementary treatment to enhance current cancer therapies.
  • The findings support Ocoxin's potential role in improving therapeutic outcomes for patients with colorectal, breast, pancreatic, and prostate cancers.

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