Development of Nanoscale Oil Bodies for Targeted Treatment of Lung Cancer
Chung-Jen Chiang, Li-Jen Lin, Chia-Pei Wu
1Department of Medical Research , China Medical University Hospital , Taichung 40447 , Taiwan.
Abstract:
Lung cancer is the most widespread disease and is frequently associated with a high level of epidermal growth factor receptor (EGFR). This study was thus conducted to provide a proof-of-concept approach for targeted therapy of lung cancer by development of nanoscale oil bodies (NOBs). This was carried out by fusion of anti-EGFR affibody (ZEGFR2) with oleosin (Ole), a structure protein of plant seed oils. The fusion protein (Ole-ZEGFR2) was produced in Escherichia coli. NOBs were spontaneously assembled from plant oil, phospholipids, and Ole-ZEGFR2. Consequently, Ole-ZEGFR2-based NOBs were selectively internalized by EGFR-positive lung cancer cells with an efficiency exceeding 90%. Furthermore, the hydrophobic anticancer drug, camptothecin (CPT), was encapsulated into Ole-ZEGFR2-based NOBs. The administration of the CPT formulation based on NOBs resulted in a strong antitumor activity both in vitro and in vivo.
Insights
Researchers developed novel nanoscale oil bodies (NOBs) for targeted lung cancer therapy. These NOBs effectively deliver anticancer drugs to epidermal growth factor receptor (EGFR)-positive cancer cells, showing significant antitumor activity.
Area of Science:
- Biotechnology
- Nanomedicine
- Oncology
Background:
- Lung cancer is a leading cause of mortality worldwide.
- High levels of epidermal growth factor receptor (EGFR) are common in lung cancer.
- Targeted therapies are crucial for improving lung cancer treatment outcomes.
Purpose of the Study:
- To develop nanoscale oil bodies (NOBs) as a targeted drug delivery system for lung cancer.
- To functionalize NOBs with an anti-EGFR affibody for specific cancer cell targeting.
- To evaluate the efficacy of drug-loaded NOBs in vitro and in vivo.
Main Methods:
- Fusion of anti-EGFR affibody (ZEGFR2) with oleosin (Ole) to create a fusion protein (Ole-ZEGFR2).
- Spontaneous assembly of NOBs using plant oil, phospholipids, and the Ole-ZEGFR2 fusion protein.
- Encapsulation of the hydrophobic anticancer drug camptothecin (CPT) into the NOBs.
- Assessment of NOB internalization by EGFR-positive lung cancer cells.
- Evaluation of antitumor activity of CPT-loaded NOBs in vitro and in vivo.
Main Results:
- Ole-ZEGFR2 fusion protein was successfully produced.
- NOBs were spontaneously assembled and characterized.
- Ole-ZEGFR2-based NOBs demonstrated selective internalization by EGFR-positive lung cancer cells (>90% efficiency).
- CPT-loaded NOBs exhibited significant antitumor activity in both in vitro and in vivo models.
Conclusions:
- Ole-ZEGFR2-based NOBs represent a promising platform for targeted lung cancer therapy.
- This approach enables efficient delivery of hydrophobic anticancer drugs to cancer cells.
- The developed NOB formulation shows strong potential for clinical translation in lung cancer treatment.
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