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

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. 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. 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. EVs with membrane-expressed bioactive molecules are a promising strategy for delivering therapeutic agents to EGFR+ colorectal cancer cells.

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Publication Details

Journal
Cancer Nanotechnology
Published
2024-08-16
DOI
https://doi.org/10.1186/s12645-024-00284-0
Citations
2
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.47

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article

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

Shi-Wei Chao, Wun-Ya Jhang, Shuo-Hung Wang, Chia-Tse Li et al.
2 citations
Cancer Nanotechnology
Extracellular vesicles in disease
0.47
article

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

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

Abstract

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. 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. 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. EVs with membrane-expressed bioactive molecules are a promising strategy for delivering therapeutic agents to EGFR+ colorectal cancer cells.

Cancer NanotechnologyVol. 15(1)
Kaohsiung Medical University (TW), Kaohsiung Medical University Chung-Ho Memorial Hospital (TW), Kaohsiung Armed Forces General Hospital (TW), Fooyin University (TW)
Ministry of Science and Technology, Taiwan, Kaohsiung Medical University, Kaohsiung Medical University Chung-Ho Memorial Hospital
Good health and well-being
Openalex Percentile: Top 36%
Extracellular vesicles in disease
0.47
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