Cancer Nanotechnology (Aug 2024)

Maximizing oxaliplatin's impact on EGFR + colorectal cancer through targeted extracellular vesicles

  • Shang-Tao Chien,
  • Yi-Jung Huang,
  • Ming-Yii Huang,
  • Yi-Ping Fang,
  • Shi-Wei Chao,
  • Chia-Tse Li,
  • Wun-Ya Jhang,
  • Yun-Han Hsu,
  • Shuo-Hung Wang,
  • Chih-Hung Chuang

DOI
https://doi.org/10.1186/s12645-024-00284-0
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 16

Abstract

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Abstract Purpose To investigate the ability of extracellular vesicles (EVs) to deliver oxaliplatin to epidermal growth factor receptor (EGFR+) colorectal cancer cells and increase oxaliplatin’s cytotoxicity. Method Oxaliplatin was passively loaded into a stable cell line expressing cetuximab in membranes. EVs were collected and characterized for size, and their ability to target EGFR+ cells was tested. Cytotoxicity experiments were performed, and a xenograft cancer animal model was used to confirm the specific accumulation of oxaliplatin-loaded EVs with cetuximab-expressing membranes in EGFR+ cells. Results EVs with cetuximab-expressing membranes were successfully produced and used to encapsulate oxaliplatin, resulting in consistently sized oxaliplatin-loaded EVs with cetuximab-expressing membranes. The oxaliplatin-loaded EVs with cetuximab-expressing membranes were specifically accumulated by EGFR+ cells, leading to significant cytotoxic effects on these cells. In the animal model, the oxaliplatin-loaded EVs with cetuximab-expressing membranes accumulated specifically in EGFR+ cells and significantly enhanced oxaliplatin’s therapeutic efficacy against EGFR+ cancer cells. Conclusion EVs with membrane-expressed bioactive molecules are a promising strategy for delivering therapeutic agents to EGFR+ colorectal cancer cells.

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