Abstract
Irinotecan (CTP-11) is a topoisomerase I inhibitor used in the treatment of colorectal cancer and non-small cell lung cancer (NSCLC). Despite an initial response to therapy, resistance to irinotecan reduces its efficacy. We isolated irinotecan-resistant human NSCLC A549 cells, termed A549/CTP-11R cells. A549/CTP-11R cells were resistant to irinotecan, as well as paclitaxel, gemcitabine and carboplatin. Curcumin, a nuclear factor-κB (NF-κB) inhibitor, increased the sensitivity to irinotecan of A549/CTP-11R cells. The expression level of Bcl-XL and X-linked inhibitor of apoptosis protein, target genes of NF-κB, in A549/CTP-11R cells was higher than that in A549 cells. Our result suggests that the addition of curcumin to irinotecan reverses irinotecan resistance in NSCLC.
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CITATION STYLE
Ikeda, R., Vermeulen, L. C., Lau, E., Jiang, Z., Pomplun, M., & Kolesar, J. M. (2010). Establishment and characterization of irinotecan-resistant human non-small cell lung cancer A549 cells. Molecular Medicine Reports, 3(6), 1031–1034. https://doi.org/10.3892/mmr.2010.366
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