TY - JOUR T1 - Synthesis and Evaluation of a Novel Deguelin Derivative, L80, which Disrupts ATP Binding to the C-terminal Domain of Heat Shock Protein 90 JF - Molecular Pharmacology JO - Mol Pharmacol SP - 245 LP - 255 DO - 10.1124/mol.114.096883 VL - 88 IS - 2 AU - Su-Chan Lee AU - Hye-Young Min AU - Hoon Choi AU - Ho Shin Kim AU - Kyong-Cheol Kim AU - So-Jung Park AU - Myeong A Seong AU - Ji Hae Seo AU - Hyun-Ju Park AU - Young-Ger Suh AU - Kyu-Won Kim AU - Hyun-Seok Hong AU - Hee Kim AU - Min-Young Lee AU - Jeewoo Lee AU - Ho-Young Lee Y1 - 2015/08/01 UR - http://molpharm.aspetjournals.org/content/88/2/245.abstract N2 - The clinical benefit of current anticancer regimens for lung cancer therapy is still limited due to moderate efficacy, drug resistance, and recurrence. Therefore, the development of effective anticancer drugs for first-line therapy and for optimal second-line treatment is necessary. Because the 90-kDa molecular chaperone heat shock protein (Hsp90) contributes to the maturation of numerous mutated or overexpressed oncogenic proteins, targeting Hsp90 may offer an effective anticancer therapy. Here, we investigated antitumor activities and toxicity of a novel deguelin-derived C-terminal Hsp90 inhibitor, designated L80. L80 displayed significant inhibitory effects on the viability, colony formation, angiogenesis-stimulating activity, migration, and invasion of a panel of non–small cell lung cancer cell lines and their sublines with acquired resistance to paclitaxel with minimal toxicity to normal lung epithelial cells, hippocampal cells, vascular endothelial cells, and ocular cells. Biochemical analyses and molecular docking simulation revealed that L80 disrupted Hsp90 function by binding to the C-terminal ATP-binding pocket of Hsp90, leading to the disruption of the interaction between hypoxia-inducible factor (HIF)-1α and Hsp90, downregulation of HIF-1α and its target genes, including vascular endothelial growth factor (VEGF) and insulin-like growth factor 2 (IGF2), and decreased the expression of various Hsp90 client proteins. Consistent with these in vitro findings, L80 exhibited significant antitumor and antiangiogenic activities in H1299 xenograft tumors. These results suggest that L80 represents a novel C-terminal Hsp90 inhibitor with effective anticancer activities with minimal toxicities. ER -