| Literature DB >> 22870135 |
Ryuji Ikeda1, Lee C Vermeulen, Elim Lau, Zhisheng Jiang, Shannon M Kavanaugh, Katsushi Yamada, Jill M Kolesar.
Abstract
Erlotinib, an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, is an effective therapy for non-small cell lung cancer (NSCLC). However, resistance to erlotinib reduces its efficacy. To investigate the basis of erlotinib resistance, we isolated erlotinib-resistant human NSCLC A549 cells, termed A549/ER cells. The A549/ER cells were found to be resistant to erlotinib, as well as paclitaxel and gemcitabine. We then performed a PCR array to investigate the resistance to erlotinib in A549/ER cells. EGFR expression in A549/ER cells was decreased compared to A549 cells. The expression of fibroblast growth factor 2 (FGF2) and p21 in A549/ER was increased when compared to A549 cells. Our results suggest that the down-regulation of EGFR and up-regulation of FGF2 is related to resistance to erlotinib in A549/ER cells.Entities:
Year: 2010 PMID: 22870135 PMCID: PMC3412472 DOI: 10.3892/ol.2010.198
Source DB: PubMed Journal: Oncol Lett ISSN: 1792-1074 Impact factor: 2.967