Abstract
Non-small cell lung cancer (NSCLC) is the most common type of lung cancer and that accounts for 85% of lung cancer patients. Although several EGFR-targeted drugs have been developed in the treatment of NSCLC, the clinical efficacy of EGFR-targeted drugs in NSCLC is limited by the occurrence of drug resistance. In this regard, Hsp90 represents great promise as a therapeutic target of cancer due to its potential to simultaneously disable multiple signaling pathways. In this study, we discovered that a natural product, flavokawain B disrupted Hsp90 chaperoning function and impaired the growth of gefitinib-resistant non-small cell lung cancer (H1975). The result suggested that flavokawain B could serve as a potential lead compound to overcome the drug resistance in cancer chemotherapy.
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Seo, Y. H., & Oh, Y. J. (2013). Synthesis of flavokawain B and its anti-Proliferative activity against gefitinib-Resistant non-Small cell lung cancer (NSCLC). Bulletin of the Korean Chemical Society, 34(12), 3782–3786. https://doi.org/10.5012/bkcs.2013.34.12.3782
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