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Establishing Dual Resistance to EGFR-TKI and MET-TKI in Lung Adenocarcinoma Cells In Vitro with a 2-step Dose-escalation Procedure
Published on: August 11, 2017
Resistance to gefitinib
Hidetaka Uramoto1, Kenji Sugio, Tsunehiro Oyama
1Second Department of Surgery, School of Medicine, University of Occupational and Environmental Health, 1-1 Iseigaoka, Yahatanishi-ku, Kitakyushu 807-8555, Japan.
Abstract:
Subsets of patients with non-small cell lung cancer (NSCLC) who carry somatic mutations in the epidermal growth factor receptor (EGFR) have responded remarkably well to a tyrosine kinase inhibitor (TKI), gefitinib. Despite the dramatic response to this inhibitor, most patients nevertheless ultimately have a relapse. We herein report a case of advanced NSCLC in a patient carrying mutated EGFR (delE746-A750) who had a relapse after dramatic improvement by gefitinib treatment. The DNA sequence of the EGFR gene in a tumor biopsy specimen obtained from the relapse site revealed the presence of a second point mutation, resulting in a threonine-to-methionine amino acid substitution at position 790 of EGFR, which could not be detected in the tumor specimen taken before the treatment. Screening subjects with EGFR mutations therefore allows us to identify patients who can be successfully treated with gefitinib. Such observations should also help us in the search for more effective therapies against a specific subset of NSCLC.
Insights
Patients with non-small cell lung cancer (NSCLC) with EGFR mutations benefit from gefitinib. However, acquired resistance, like the T790M mutation, can cause relapse, necessitating new therapeutic strategies.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Non-small cell lung cancer (NSCLC) patients with specific epidermal growth factor receptor (EGFR) mutations often respond to tyrosine kinase inhibitors (TKIs) like gefitinib.
- Despite initial efficacy, acquired resistance frequently leads to treatment relapse in these patients.
Observation:
- A case study of advanced NSCLC with an EGFR delE746-A750 mutation treated with gefitinib is presented.
- The patient experienced initial dramatic improvement followed by relapse.
Findings:
- A secondary EGFR T790M mutation was identified in tumor biopsy from the relapse site.
- This T790M mutation was not present in the pre-treatment tumor biopsy, indicating acquired resistance.
Implications:
- Screening for EGFR mutations aids in identifying patients suitable for gefitinib therapy.
- The emergence of acquired resistance mutations like T790M highlights the need for developing alternative or combination therapies for NSCLC.
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