Understanding resistance to EGFR inhibitors—impact on future treatment strategies
Open accessAbstract
EGFR is a tyrosine kinase that participates in the regulation of cellular homeostasis. Following ligand binding, EGFR stimulates downstream cell signaling cascades that influence cell proliferation, apoptosis, migration, survival and complex processes, including angiogenesis and tumorigenesis. EGFR has been strongly implicated in the biology of human epithelial malignancies, with therapeutic applications in cancers of the colon, head and neck, lung, and pancreas. Accordingly, targeting EGFR has been intensely pursued, with the development of a series of promising molecular inhibitors for use in clinical oncology. As is common in cancer therapy, challenges with respect to treatment resistance emerge over time. This situation is certainly true of EGFR inhibitor therapies, where intrinsic and acquired resistance is now well recognized. In this Review, we provide a brief overview regarding the biology of EGFR, preclinical and clinical development of EGFR inhibitors, and molecular mechanisms that underlie the development of treatment resistance. A greater understanding of the mechanisms that lead to EGFR resistance may provide valuable insights to help design new strategies that will enhance the impact of this promising class of inhibitors for the treatment of cancer.
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Other PI3K pathway activating lesions commonly found in GBM, such as activation of other RTKs, could also promote increased LDLR expression.
“Therefore, other PI3K pathway activating lesions commonly found in GBM, such as the activation of other RTKs (6, 12, 39), could also promote increased LDLR expression.”
From An LXR Agonist Promotes Glioblastoma Cell Death through Inhibition of an EGFR/AKT/SREBP-1/LDLR–Dependent Pathway (2011) · cites this paper as [39]
The ‘Role of IGF-1R in resistance to EGFR inhibitors’ section reports that IGF-1R, an RTK, was upregulated in two primary GBM cell lines and sustained PI3K/AKT signaling. That supports the citation attached to activation of other RTKs, but the section does not establish that such activation is commonly found in GBM. The proposed increase in LDLR expression is the citing authors’ own inference, not the point to which this citation is attached. (LLM, conf=0.82)
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Yes and Lyn play a role in nuclear translocation of the Epidermal Growth Factor Receptor
Iida, M., Brand, T. M., Campbell, D., Li, C.-R., & Wheeler, D. (2012) · Oncogene · doi:10.1038/onc.2012.90 · Cited by 84 · see citing works
Self-citationUnexpected Off-Targets and Paradoxical Pathway Activation by Kinase Inhibitors
Hantschel, O. D. (2014) · ACS Chemical Biology · doi:10.1021/cb500886n · Cited by 87 · see citing works
Epidermal growth factor receptor inhibits colitis-associated cancer in mice
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InsR/IGF1R Pathway Mediates Resistance to EGFR Inhibitors in Glioblastoma
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Antibodies directed against receptor tyrosine kinases
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RasGRP1 opposes proliferative EGFR–SOS1–Ras signals and restricts intestinal epithelial cell growth
Depeille, P., Henricks, L. M., van de Ven, R. A. H., Lemmens, E., Wang, C.-Y., Matli, M., Werb, Z., Haigis, K. M., Donner, D., Warren, R., et al. (2015) · Nature Cell Biology · doi:10.1038/ncb3175 · Cited by 80 · see citing works
Panitumumab in Patients with KRAS Wild-Type Colorectal Cancer after Progression on Cetuximab
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The proto-oncogene KRAS is targeted by miR-200c
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Cetuximab Resistance in Head and Neck Cancer Is Mediated by EGFR-K521 Polymorphism
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- Authors
- Wheeler, D. L., Dunn, E. F., & Harari, P. M.
- Affiliations
- University of Wisconsin–Madison (US)
- Corresponding author
- Wheeler, Deric L.
- Venue
- Nature Reviews Clinical Oncology
- Published
- 2010-06-15
- Volume
- 7
- Issue
- 9
- Pages
- 493-507
- ISSN
- 1759-4774 (ISSN-L)
- 1759-4782
- PMC
- PMC2929287
- OpenAlex
- W2053439872
- Cited by
- 683
- References
- 182
- Citations by year
- 2026: 21 · 2025: 20 · 2024: 35 · 2023: 29 · 2022: 31 · 2021: 29 · 2020: 44 · 2019: 25 · 2018: 36 · 2017: 50 · 2016: 46 · 2015: 61 · 2014: 66 · 2013: 68 · 2012: 64
- FWCI
- 6.61
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Clinical Oncology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (5t32ca009614-25)
- U.S. Public Health Service (P30CAO14520)
- National Cancer Institute (T-32 CA 0096-14, R01CA113448)
- National Center for Research Resources (UL1RR025011)
- Topics
- Health Sciences › Medicine › Oncology › HER2/EGFR in Cancer Research
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
- Health Sciences › Medicine › Oncology › Colorectal Cancer Treatments and Studies
- Keywords
- EGFR inhibitors, EGFR, acquired drug resistance, intrinsic resistance, tyrosine kinase inhibitors, resistance mechanisms, EGFR signaling, epithelial malignancies, lung cancer, head and neck cancer, colon cancer, pancreatic cancer, combination therapy
- MeSH terms
- Cetuximab, Erlotinib Hydrochloride, Gefitinib, Panitumumab, Antibodies, Monoclonal, Antineoplastic Agents, Humans, Neoplasms, Proto-Oncogene Proteins, Quinazolines, Proto-Oncogene Proteins p21(ras), Treatment Outcome, Disease Progression, ras Proteins, Drug Resistance, Neoplasm, Protein Kinase Inhibitors, Antibodies, Monoclonal, Humanized, ErbB Receptors
About these checks
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