Discovery of Mcl-1-specific inhibitor AZD5991 and preclinical activity in multiple myeloma and acute myeloid leukemia
Autor: | Nancy Su, Brian Aquila, Gareth P. Gregory, Stephen Fawell, J. Adam Hendricks, Ammar Adam, Lawrence H. Boise, Jeffrey W. Johannes, Kevin J. Embrey, Edwin Clark, Philip B. Rawlins, Justin Cidado, Francis D. Gibbons, Ricky W. Johnstone, Qing Ye, Elisabetta Chiarparin, Steven L. Kazmirski, Michelle Lamb, J. Paul Secrist, Wenzhan Yang, Alexander Hird, Daniel W. Robbins, Adriana E. Tron, Alwin Schuller, Martin J. Packer, David J. Hargreaves, Xiaolan Zheng, Matthew A. Belmonte, Eric Gangl, Ajay K. Nooka, Shannon M. Matulis, Jason Grant Kettle, Bo Peng, David Matthew Wilson |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Myeloid General Physics and Astronomy Apoptosis Mice SCID medicine.disease_cause Crystallography X-Ray Bortezomib chemistry.chemical_compound Mice 0302 clinical medicine immune system diseases hemic and lymphatic diseases lcsh:Science Multiple myeloma Sulfonamides Multidisciplinary Myeloid leukemia Leukemia Leukemia Myeloid Acute medicine.anatomical_structure 030220 oncology & carcinogenesis Multiple Myeloma medicine.drug Science Antineoplastic Agents General Biochemistry Genetics and Molecular Biology Article 03 medical and health sciences Rats Nude Cell Line Tumor medicine Animals Humans neoplasms Venetoclax business.industry General Chemistry medicine.disease Bridged Bicyclo Compounds Heterocyclic Xenograft Model Antitumor Assays Rats Mice Inbred C57BL 030104 developmental biology chemistry Cancer cell Cancer research Myeloid Cell Leukemia Sequence 1 Protein lcsh:Q Carcinogenesis business |
Zdroj: | Nature Communications, Vol 9, Iss 1, Pp 1-14 (2018) Nature Communications |
ISSN: | 2041-1723 |
DOI: | 10.1038/s41467-018-07551-w |
Popis: | Mcl-1 is a member of the Bcl-2 family of proteins that promotes cell survival by preventing induction of apoptosis in many cancers. High expression of Mcl-1 causes tumorigenesis and resistance to anticancer therapies highlighting the potential of Mcl-1 inhibitors as anticancer drugs. Here, we describe AZD5991, a rationally designed macrocyclic molecule with high selectivity and affinity for Mcl-1 currently in clinical development. Our studies demonstrate that AZD5991 binds directly to Mcl-1 and induces rapid apoptosis in cancer cells, most notably myeloma and acute myeloid leukemia, by activating the Bak-dependent mitochondrial apoptotic pathway. AZD5991 shows potent antitumor activity in vivo with complete tumor regression in several models of multiple myeloma and acute myeloid leukemia after a single tolerated dose as monotherapy or in combination with bortezomib or venetoclax. Based on these promising data, a Phase I clinical trial has been launched for evaluation of AZD5991 in patients with hematological malignancies (NCT03218683). High expression of Mcl-1 promotes tumorigenesis and resistance to anticancer therapies. Here they report a macrocyclic molecule with high selectivity and affinity for Mcl-1 that exhibits potent anti-tumor effects as single agent and in combination with bortezomib or venetoclax in preclinical models of multiple myeloma and acute myeloid leukemia. |
Databáze: | OpenAIRE |
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