Repurposing of Cetuximab in antibody-directed chemotherapy-loaded nanoparticles in EGFR therapy-resistant pancreatic tumours
Open accessAbstract
The use of CTX as a targeting agent for camptothecin-loaded polymeric nanoparticles directed against KRAS mutant CTX-resistant cancer cells was investigated. CTX increased CPT internalisation into cancer cells resulting in elevated cancer cell death.
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EGFR is a cell surface receptor expressed in many different types of cells, especially overexpressed in cancer cells.
“EGFR is a cell surface receptor expressed in many different types of cells, especially overexpressed in cancer cells.195”
From Smart nanoparticles for cancer therapy (2023) · cites this paper as [195]
The CTX coupled nano drug delivery system enhanced the ability of NPs to target the cell surface by interacting with EGFR.
“The results confirmed that the CTX coupled nano drug delivery system enhanced the ability of NPs to target the cell surface by interacting with EGFR.195”
From Smart nanoparticles for cancer therapy (2023) · cites this paper as [195]
The overexpression of EGFR is closely related to the differentiation and migration of cancer cells.
“Researchers have shown that the overexpression of EGFR is closely related to the differentiation and migration of cancer cells.”
From Smart nanoparticles for cancer therapy (2023) · cites this paper as [195]
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Smart nanoparticles for cancer therapy
Sun, L., Liu, H., Ye, Y., Lei, Y., Islam, R., Tan, S., Tong, R., Miao, Y.-B., & Cai, L. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01642-x · Cited by 1,073 · see citing works
- Authors
- McDaid, W. J., Greene, M. K., Johnston, M. C., Pollheimer, E., Smyth, P., McLaughlin, K., Van Schaeybroeck, S., Straubinger, R. M., Longley, D. B., & Scott, C. J.
- Affiliations
- Queen's University Belfast (GB)
- Centre for Cancer Research and Cell Biology
- State University of New York (US)
- Corresponding author
- Scott, Christopher J.
- ORCID
- Venue
- Nanoscale
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2019
- Volume
- 11
- Issue
- 42
- Pages
- 20261-20273
- ISSN
- 2040-3364 (ISSN-L)
- 2040-3372
- PMC
- PMC6861736
- OpenAlex
- W2981159739
- Cited by
- 58
- References
- 46
- Citations by year
- 2026: 5 · 2025: 8 · 2024: 9 · 2023: 7 · 2022: 12 · 2021: 9 · 2020: 8
- FWCI
- 2.05
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nanoscale (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Research Portal (Queen's University Belfast) (submittedVersion, other-oa)
- Funders
- Medical Research Council (MRC grant 1598124, MC_PC_15013)
- National Institutes of Health (R21CA168454, R01CA198096)
- Topics
- Physical Sciences › Materials Science › Biomaterials › Nanoparticle-Based Drug Delivery
- Health Sciences › Medicine › Oncology › Pancreatic and Hepatic Oncology Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Interference and Gene Delivery
- Keywords
- cetuximab, camptothecin, polymeric nanoparticles, PLGA nanoparticles, EGFR, KRAS mutation, pancreatic cancer, drug resistance, targeted drug delivery, PANC-1 cells, tumor growth inhibition
- MeSH terms
- Cetuximab, Ado-Trastuzumab Emtansine, Animals, Female, Humans, Neoplasm Proteins, Pancreatic Neoplasms, Mice, SCID, Immunoconjugates, Drug Resistance, Neoplasm, Xenograft Model Antitumor Assays, HCT116 Cells, Mice, Nanoparticles, ErbB Receptors
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