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Updated: Aug 14, 2026

Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
[Epidermal growth factor receptor (EGFR): therapeutic target in the treatment of lung adenocarcinoma]
Richárd Schwab1, István Peták, Ferenc Pintér
1Semmelweis Egyetem, Altalános Orvostudományi Kar, I. Patológiai es Kísérleti Rákkutató Intézet.
Abstract:
Revolution in biotechnology made possible to identify those gene errors, which via their encoded proteins (mostly kinase enzymes) are key players in tumor development, growth and progression, and could be considered as molecular targets in tumor diagnosis and therapy. Activity of EGFR (epidermal growth factor receptor), an outstanding representative of the regulatory cell surface receptors, can be inhibited by drugs proved for clinical use. In the past year many groups observed that those lung adenocarcinoma cells, which contain activating mutation in the tyrosine kinase domain of EGFR show remarkable sensitivity to anti-EGFR compounds. The basis of the effective therapy is the identification of the mutations. The clinical advantage of EGFR is an example from the coming age of tumor chemotherapy, when the presence of molecular targets will guide the therapeutic choice.
Insights
Biotechnology advances enable targeting gene errors in cancer. Identifying mutations in epidermal growth factor receptor (EGFR) allows effective lung adenocarcinoma treatment with anti-EGFR drugs.
Area of Science:
- Biotechnology and Molecular Oncology
Background:
- Gene errors encode proteins, particularly kinase enzymes, crucial for tumor development.
- Epidermal growth factor receptor (EGFR) is a key cell surface receptor involved in tumor progression.
- Activating mutations in EGFR's tyrosine kinase domain are linked to lung adenocarcinoma sensitivity to targeted therapies.
Purpose of the Study:
- To highlight the role of gene mutations in cancer therapy.
- To emphasize the significance of identifying specific molecular targets for effective treatment.
Main Methods:
- Leveraging biotechnological advancements for gene error identification.
- Observing the sensitivity of lung adenocarcinoma cells with EGFR mutations to anti-EGFR compounds.
Main Results:
- Biotechnology facilitates the identification of gene errors driving tumor growth.
- Lung adenocarcinoma cells with specific EGFR mutations demonstrate high sensitivity to anti-EGFR drugs.
- Mutation identification is the foundation for effective targeted cancer therapy.
Conclusions:
- Targeted therapies based on molecular diagnostics represent a new era in cancer chemotherapy.
- Identifying EGFR mutations guides therapeutic choices for improved patient outcomes.
- Personalized medicine, guided by molecular targets, is crucial for future tumor treatment.
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