bioAffinity’s siRNA Therapy Shows Selective Skin Cancer Cell Kill in Preclinical Study

  • bioAffinity’s proprietary siRNA therapy demonstrated selective cytotoxicity to squamous and basal skin cancer cells in vitro while sparing healthy cells.
  • The findings will be presented at the RNATx Symposium on June 24-26, 2026.
  • The research builds on earlier discoveries targeting CD320 and LRP2 receptors, patented in 2025 (U.S. Patent No. 12,305,171).
  • No human trials have been conducted; preclinical results require further validation.

bioAffinity’s findings contribute to the growing field of RNA therapeutics, particularly for non-melanoma skin cancers, which affect millions annually. The company is leveraging its expertise in diagnostics (e.g., CyPath® Lung) to expand into targeted oncology treatments, a strategic shift that could diversify its revenue streams if preclinical success translates clinically.

Clinical Translation Risk
Whether in vitro selectivity will translate to human trials, given the historical challenges of siRNA therapies.
Regulatory Pathway
The pace at which bioAffinity can secure FDA approval for an IND application and advance into clinical testing.
Competitive Positioning
How this technology differentiates from existing topical treatments or emerging RNA-based cancer therapies in development.