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Targeting MCL-1 in hematologic malignancies: Rationale and progress

  • Andrew H. Wei
  • , Andrew W. Roberts
  • , Andrew Spencer
  • , Aaron Seth Rosenberg
  • , David Siegel
  • , Roland B. Walter
  • , Sean Caenepeel
  • , Paul Hughes
  • , Zach McIver
  • , Khalid Mezzi
  • , Phuong Khanh Morrow
  • , Anthony Stein
  • Monash University
  • University of Melbourne
  • University of California at Davis
  • Fred Hutchinson Cancer Research Center
  • Amgen Incorporated
  • City of Hope National Med Center

Research output: Contribution to journal › Review article › peer-review

189 Scopus citations

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.

Original languageEnglish
Article number100672
JournalBlood Reviews
Volume44
DOIs
StatePublished - Nov 2020

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acute myeloid leukemia
  • BH3-mimetic
  • MCL-1 inhibitor
  • Multiple myeloma
  • Non-Hodgkin lymphoma

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