Doxycycline, salinomycin, monensin and ivermectin repositioned as cancer drugs

Anna Markowska1, Joanna Kaysiewicz2, Janina Markowska3

  • 1Department of Perinatology and Women's Diseases, Poznan University of Medical Sciences, Polna 33, 60-545 Poznan, Poland.

Insights

Novel antibiotics like doxycycline, salinomycin, monensin, and ivermectin show significant anti-tumor activity. These repurposed drugs could offer new pathways for treating cancer cells and cancer stem cells (CSCs).

Area of Science:

  • Oncology
  • Pharmacology
  • Infectious Diseases

Background:

  • Chemotherapy is a standard cancer treatment targeting cellular structures like DNA.
  • Repurposing existing antibiotics as anticancer agents is an emerging therapeutic strategy.
  • Doxycycline, salinomycin, monensin, and ivermectin are widely available antibiotics with known antimicrobial and antiparasitic properties.

Purpose of the Study:

  • To review the emerging anticancer applications of doxycycline (DOX), salinomycin (SAL), monensin (MON), and ivermectin (IVR).
  • To highlight their potential as novel agents against cancer cells and cancer stem cells (CSCs).
  • To explore their suitability for integration into standard oncological therapy.

Main Methods:

  • Literature review of existing studies on the selected antibiotics.
  • Analysis of data demonstrating the anti-tumor activity of doxycycline, salinomycin, monensin, and ivermectin.
  • Evaluation of their potential to target cancer cells and cancer stem cells (CSCs).

Main Results:

  • The reviewed antibiotics exhibit significant potential for eradicating cancer cells.
  • These agents also demonstrate efficacy against cancer stem cells (CSCs), which are crucial for tumor recurrence.
  • Their established safety profiles and availability support their consideration for oncological use.

Conclusions:

  • Doxycycline, salinomycin, monensin, and ivermectin represent promising novel anticancer agents.
  • These repurposed antibiotics warrant further investigation for clinical application in various cancer types.
  • Their potential to target both cancer cells and CSCs could lead to more effective cancer treatments.

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