| Literature DB >> 32204955 |
Andrew H Wei1, Andrew W Roberts2, Andrew Spencer3, Aaron Seth Rosenberg4, David Siegel5, Roland B Walter6, Sean Caenepeel7, Paul Hughes7, Zach McIver7, Khalid Mezzi7, Phuong Khanh Morrow7, Anthony Stein8.
Abstract
Myeloid cell leukemia sequence 1 (MCL-1) is an antiapoptotic protein that plays a key role in promoting cell survival in multiple myeloma (MM), acute myeloid leukemia (AML), and non-Hodgkin lymphoma (NHL). Overexpression of MCL-1 is associated with treatment resistance and poor prognosis; thus, MCL-1 inhibitors are rational therapeutic options for malignancies depending on MCL-1. Several MCL-1 inhibitors have entered clinical trials, including AZD5991, S64315, AMG 176, and AMG 397. A key area of investigation is whether MCL-1 inhibitors will complement the activity of BCL-2 inhibitors, such as venetoclax, and synergistically enhance anti-tumor efficacy when given in combination with other anti-cancer drugs. Another important question is whether a safe therapeutic window can be found for this new class of inhibitors. In summary, inhibition of MCL-1 shows potential as a treatment for hematologic malignancies and clinical evaluation of MCL-1 inhibitors is currently underway.Entities:
Keywords: Acute myeloid leukemia; BH3-mimetic; MCL-1 inhibitor; Multiple myeloma; Non-Hodgkin lymphoma
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Year: 2020 PMID: 32204955 PMCID: PMC7442684 DOI: 10.1016/j.blre.2020.100672
Source DB: PubMed Journal: Blood Rev ISSN: 0268-960X Impact factor: 8.250