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Therapeutic application of extracellular vesicular EGFR isoform D as a co-drug to target squamous cell cancers with tyrosine kinase inhibitors.
- Source :
-
Developmental cell [Dev Cell] 2024 Aug 19; Vol. 59 (16), pp. 2189-2202.e8. Date of Electronic Publication: 2024 Jul 31. - Publication Year :
- 2024
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Abstract
- Targeting wild-type epidermal growth factor receptor (EGFR) using tyrosine kinase inhibitors (TKIs) never achieved its purported success in cancers such as head and neck squamous cell carcinoma, which are largely EGFR-dependent. We had previously shown that exceptional responders to TKIs have a genetic aberration that results in overexpression of an EGFR splice variant, isoform D (IsoD). IsoD lacks an integral transmembrane and kinase domain and is secreted in extracellular vesicles (EVs) in TKI-sensitive patient-derived cultures. Remarkably, the exquisite sensitivity to TKIs could be transferred to TKI-resistant tumor cells, and IsoD protein in the EV is necessary and sufficient to transfer the phenotype in vitro and in vivo across multiple models and drugs. This drug response requires an intact endocytic mechanism, binding to full-length EGFR, and signaling through Src-phosphorylation within the endosomal compartment. We propose a therapeutic strategy using EVs containing EGFR IsoD as a co-drug to expand the use of TKI therapy to EGFR-driven cancers.<br />Competing Interests: Declaration of interests N.G.I. has/had a consulting or advisory role in PairX Therapeutics, Verimmune therapeutics, and Invivo surgical; received honoraria from Agilent, and research funding from Merck, all of which are outside this submitted work. D.S.W.T. received honoraria from Bristol-Myers Squibb, Takeda Pharmaceuticals, Novartis, Roche, and Pfizer; has consulting or advisory role in Novartis, Merck, Loxo Oncology, AstraZeneca, Roche, and Pfizer and received research funding from Novartis (Inst), GlaxoSmithKline (Inst), and AstraZeneca (Inst), outside this submitted work. N.G.I., D.S.W.T., S.Y.T., H.S.L., F.T.C., and D.M.R.-J. are listed as co-inventors on the patent application entitled “Method of Modulating Sensitivity To Tyrosine Kinase Inhibitor” (International Publication: WO2022045976A1), which describes a significant proportion of the data here.<br /> (Copyright © 2024 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Humans
Mice
Cell Line, Tumor
Drug Resistance, Neoplasm drug effects
Head and Neck Neoplasms drug therapy
Head and Neck Neoplasms metabolism
Head and Neck Neoplasms pathology
Head and Neck Neoplasms genetics
Phosphorylation drug effects
Signal Transduction drug effects
Squamous Cell Carcinoma of Head and Neck drug therapy
Squamous Cell Carcinoma of Head and Neck metabolism
Squamous Cell Carcinoma of Head and Neck pathology
Squamous Cell Carcinoma of Head and Neck genetics
Carcinoma, Squamous Cell drug therapy
Carcinoma, Squamous Cell metabolism
Carcinoma, Squamous Cell pathology
ErbB Receptors metabolism
ErbB Receptors antagonists & inhibitors
ErbB Receptors genetics
Extracellular Vesicles metabolism
Protein Isoforms metabolism
Protein Isoforms genetics
Tyrosine Kinase Inhibitors pharmacology
Tyrosine Kinase Inhibitors therapeutic use
Subjects
Details
- Language :
- English
- ISSN :
- 1878-1551
- Volume :
- 59
- Issue :
- 16
- Database :
- MEDLINE
- Journal :
- Developmental cell
- Publication Type :
- Academic Journal
- Accession number :
- 39089249
- Full Text :
- https://doi.org/10.1016/j.devcel.2024.07.003