Engineered extracellular vesicles with polypeptide for targeted delivery of doxorubicin against EGFR‑positive tumors

Yuqing Yang1, Fang Wang2, Yuqin Li1

  • 1Department of Pharmacology, Jinan University, Guangzhou, Guangdong 510632, P.R. China.

Oncology Reports
|September 27, 2024
PubMed

Insights

Engineered extracellular vesicles (EVs) loaded with doxorubicin target and kill epidermal growth factor receptor (EGFR)-positive tumor cells effectively. This novel drug delivery system shows higher safety and accuracy than traditional chemotherapy.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Oncology

Background:

  • Chemotherapy faces challenges with tumor-specific drug delivery.
  • Extracellular vesicles (EVs) show promise as biocompatible drug carriers.
  • Targeting epidermal growth factor receptor (EGFR) is crucial for certain cancers.

Purpose of the Study:

  • To develop GE11 peptide-modified extracellular vesicles (GE11-EVs) for targeted delivery of doxorubicin (Dox).
  • To evaluate the efficacy and safety of Dox-GE11-EVs in EGFR-positive tumor cells.

Main Methods:

  • Formulation of GE11 peptide-modified EVs loaded with doxorubicin (Dox-GE11-EVs).
  • In vitro assessment of targeting efficiency, drug delivery, cell proliferation inhibition, and apoptosis induction in EGFR-positive tumor cells.
  • Evaluation of cytotoxicity on normal cells.

Main Results:

  • GE11-EVs demonstrated highly efficient targeting and drug delivery to EGFR-positive tumor cells.
  • Dox-GE11-EVs significantly inhibited tumor cell proliferation and increased apoptosis compared to free Dox or non-modified EVs.
  • Dox-GE11-EVs exhibited limited cytotoxicity to normal cells, unlike free Dox or Dox-EVs.

Conclusions:

  • Engineered Dox-GE11-EVs provide accurate and safer treatment for EGFR-positive tumors.
  • This targeted drug delivery system overcomes limitations of traditional chemotherapy.