Neuroendocrine Differentiation in Acquired Resistance to Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor.
- Author:
Youjin CHANG
1
;
Seon Ye KIM
;
Yun Jung CHOI
;
Kwang Sup SO
;
Jin Kyung RHO
;
Woo Sung KIM
;
Jae Cheol LEE
;
Jin Haeng CHUNG
;
Chang Min CHOI
Author Information
- Publication Type:Original Article
- Keywords: Small Cell Lung Carcinoma; Cell Transformation, Neoplastic; Drug Resistance, Neoplasm
- MeSH: 1-Methyl-3-isobutylxanthine; Adenocarcinoma; Blotting, Western; Cell Line; Cell Transformation, Neoplastic; Chromogranin A; Cisplatin; Drug Resistance, Neoplasm; Epidermal Growth Factor; Etoposide; Humans; Lung; Lung Neoplasms; Parents; Piperidines; Poly(ADP-ribose) Polymerases; Protein-Tyrosine Kinases; Quinazolines; Receptor, Epidermal Growth Factor; Small Cell Lung Carcinoma; Synaptophysin; Erlotinib Hydrochloride
- From:Tuberculosis and Respiratory Diseases 2013;75(3):95-103
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND: Small cell lung cancer (SCLC) transformation during epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) treatment in lung cancer has been suggested as one of possible resistance mechanisms. METHODS: We evaluated whether SCLC transformation or neuroendocrine (NE) differentiation can be found in the cell line model. In addition, we also investigated its effect on responses to conventional chemotherapeutic drugs of the SCLC treatment. RESULTS: Resistant cell lines to various kinds of EGFR-TKIs such as gefitinib, erlotinib, CL-387,785 and ZD6474 with A549, PC-9 and HCC827 lung adenocarcinoma cell lines were established. Among them, two resistant cell lines, A549/GR (resistant to gefitinib) and PC-9/ZDR (resistant to ZD6474) showed increased expressions of CD56 while increased synaptophysin, Rb, p16 and poly(ADP-ribose) polymerase were found only in A549/GR in western blotting, suggesting that NE differentiation occurred in A549/GR. A549/GR cells were more sensitive to etoposide and cisplatin, chemotherapeutic drugs for SCLC, compared to parental cells. Treatment with cAMP and IBMX induced synaptophysin and chromogranin A expression in A549 cells, which also made them more sensitive to etoposide and cisplatin than parental cells. Furthermore, we found a tissue sample from a patient which showed increased expressions of CD56 and synaptophysin after development of resistance to erlotinib. CONCLUSION: NE differentiation can occur during acquisition of resistance to EGFR-TKI, leading to increased chemosensitivity.
