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6 results on '"Pan, Roy D."'

1. Isoquinoline thiosemicarbazone displays potent anticancer activity with in vivo efficacy against aggressive leukemias

Author

Sun, Daniel L, Poddar, Soumya, Pan, Roy D, Rosser, Ethan W, Abt, Evan R, Van Valkenburgh, Juno, Le, Thuc M, Lok, Vincent, Hernandez, Selena P, Song, Janet, Li, Joanna, Turlik, Aneta, Chen, Xiaohong, Cheng, Chi-An, Chen, Wei, Mona, Christine E, Stuparu, Andreea D, Vergnes, Laurent, Reue, Karen, Damoiseaux, Robert, Zink, Jeffrey I, Czernin, Johannes, Donahue, Timothy R, Houk, Kendall N, Jung, Michael E, and Radu, Caius G

Subjects
Medicinal and Biomolecular Chemistry, Organic Chemistry, Chemical Sciences, Genetics, Orphan Drug, Rare Diseases, Cancer, Hematology, 5.1 Pharmaceuticals, Pharmacology and Pharmaceutical Sciences, Medicinal and biomolecular chemistry, Organic chemistry
Abstract

A potent class of isoquinoline-based α-N-heterocyclic carboxaldehyde thiosemicarbazone (HCT) compounds has been rediscovered; based upon this scaffold, three series of antiproliferative agents were synthesized through iterative rounds of methylation and fluorination modifications, with anticancer activities being potentiated by physiologically relevant levels of copper. The lead compound, HCT-13, was highly potent against a panel of pancreatic, small cell lung carcinoma, prostate cancer, and leukemia models, with IC50 values in the low-to-mid nanomolar range. Density functional theory (DFT) calculations showed that fluorination at the 6-position of HCT-13 was beneficial for ligand-copper complex formation, stability, and ease of metal-center reduction. Through a chemical genomics screen, we identify DNA damage response/replication stress response (DDR/RSR) pathways, specifically those mediated by ataxia-telangiectasia and Rad3-related protein kinase (ATR), as potential compensatory mechanism(s) of action following HCT-13 treatment. We further show that the cytotoxicity of HCT-13 is copper-dependent, that it promotes mitochondrial electron transport chain (mtETC) dysfunction, induces production of reactive oxygen species (ROS), and selectively depletes guanosine nucleotide pools. Lastly, we identify metabolic hallmarks for therapeutic target stratification and demonstrate the in vivo efficacy of HCT-13 against aggressive models of acute leukemias in mice.

Published
2020

3. Evaluation of Potent Isoquinoline-Based Thiosemicarbazone Antiproliferatives Against Solid Tumor Models

Author

Sun, Daniel, primary, Poddar, Soumya, primary, Pan, Roy D., primary, Van Valkenburgh, Juno, primary, Rosser, Ethan, primary, Abt, Evan, primary, Lok, Vincent, primary, Capri, Joseph, primary, Hernandez, Selena, primary, Song, Janet, primary, Li, Joanna, primary, Vergnes, Laurent, primary, Cabebe, Anthony, primary, Armstrong, Wesley, primary, Plamthottam, Sheba, primary, Steele, Dalton, primary, Osto, Corey, primary, Stuparu, Andreea, primary, Le, Thuc, primary, Reue, Karen, primary, Damoiseaux, Robert, primary, Czernin, Johanes, primary, Jung, Michael, primary, and Radu, Caius, primary

Published
2019
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6. Isoquinoline thiosemicarbazone displays potent anticancer activity with in vivoefficacy against aggressive leukemiasThe authors declare the following competing financial interest(s): C. G. R., J. C., and M. E. J. are co-founders of Trethera Corporation. They and the University of California hold equity in Trethera Corporation. The University of California has patented additional intellectual property for thiosemicarbazone-based antiproliferative compounds.Electronic supplementary information (ESI) available. See DOI: 10.1039/c9md00594c

Author

SunThese authors contributed equally. EWR, Daniel L., RDP, manuscript., CGR wrote the, Poddar, Soumya, Pan, Roy D., Rosser, Ethan W., Abt, Evan R., Van Valkenburgh, Juno, Le, Thuc M., Lok, Vincent, Hernandez, Selena P., Song, Janet, Li, Joanna, Turlik, Aneta, Chen, Xiaohong, Cheng, Chi-An, Chen, Wei, Mona, Christine E., Stuparu, Andreea D., Vergnes, Laurent, Reue, Karen, Damoiseaux, Robert, Zink, Jeffrey I., Czernin, Johannes, Donahue, Timothy R., Houk, Kendall N., Jung, Michael E., and Radu, Caius G.

Abstract

A potent class of isoquinoline-based α-N-heterocyclic carboxaldehyde thiosemicarbazone (HCT) compounds has been rediscovered; based upon this scaffold, three series of antiproliferative agents were synthesized through iterative rounds of methylation and fluorination modifications, with anticancer activities being potentiated by physiologically relevant levels of copper. The lead compound, HCT-13, was highly potent against a panel of pancreatic, small cell lung carcinoma, prostate cancer, and leukemia models, with IC50values in the low-to-mid nanomolar range. Density functional theory (DFT) calculations showed that fluorination at the 6-position of HCT-13was beneficial for ligand-copper complex formation, stability, and ease of metal-center reduction. Through a chemical genomics screen, we identify DNA damage response/replication stress response (DDR/RSR) pathways, specifically those mediated by ataxia-telangiectasia and Rad3-related protein kinase (ATR), as potential compensatory mechanism(s) of action following HCT-13treatment. We further show that the cytotoxicity of HCT-13is copper-dependent, that it promotes mitochondrial electron transport chain (mtETC) dysfunction, induces production of reactive oxygen species (ROS), and selectively depletes guanosine nucleotide pools. Lastly, we identify metabolic hallmarks for therapeutic target stratification and demonstrate the in vivoefficacy of HCT-13against aggressive models of acute leukemias in mice.

Published
2020
Full Text
View/download PDF

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