Breakthrough Cancer Treatment: Dual-Drug Nanoparticles Double Survival Rates in Mice

December 23, 2024
Breakthrough Cancer Treatment: Dual-Drug Nanoparticles Double Survival Rates in Mice
  • Researchers at Tel Aviv University have developed a groundbreaking platform for delivering two cancer-fighting drugs simultaneously, significantly enhancing treatment effectiveness while minimizing side effects, as detailed in a study published in Science Advances on December 23, 2024.

  • The innovative platform utilizes biodegradable nanoparticles loaded with FDA-approved drug pairs: BRAF and MEK inhibitors for melanoma, and PARP and PD-L1 inhibitors for BRCA-mutated breast cancer.

  • Experimental results demonstrated that the dual-drug delivery method significantly outperformed traditional separate drug administration, using doses 30 times lower than previous studies and resulting in a 2.5-fold improvement in time to progression and a twofold increase in median survival for treated mice.

  • Mice treated with the nanoparticles demonstrated remarkable longevity, living twice as long as those receiving free drugs and three times longer than untreated mice.

  • These nanoparticles are engineered to target cancer cells by attaching to sulfate groups that specifically bind to P-selectin, a protein found in high levels on cancer cells and their associated blood vessels.

  • This new method addresses the common issue in cancer therapies where drugs fail to reach tumors simultaneously due to differing chemical properties, which can diminish their combined effectiveness.

  • In controlled studies, untreated mice exhibited survival rates three times lower than those treated with the nanoparticles, underscoring the method's effectiveness.

  • The platform was rigorously tested on 3D cancer cell models and animal models simulating primary melanoma and breast cancer tumors, showing targeted accumulation in primary tumors without harming healthy tissues.

  • Notably, the nanoparticles successfully crossed the blood-brain barrier, allowing for effective treatment of brain metastases while sparing healthy brain tissue.

  • This versatile nanoparticle technology is adaptable for various drug pairs and cancers, with potential applications for other tumors expressing P-selectin, such as pancreatic cancer and glioblastoma.

  • Prof. Ronit Satchi-Fainaro, who led the study alongside doctoral student Shani Koshrovski-Michael, emphasized that the technology enhances the effects of multiple drugs, improving cancer treatment outcomes.

  • The study, which included contributions from researchers across Israel, Italy, Portugal, and the Netherlands, was published in the peer-reviewed journal Science Advances.

Summary based on 3 sources


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