Mebendazole Mediates Proteasomal Degradation of GLI Transcription Factors in Acute Myeloid Leukemia

Fabian Freisleben1, Franziska Modemann1,2, Jana Muschhammer1

  • 1Department of Oncology, Hematology and Bone Marrow Transplantation with Section Pneumology, Hubertus Wald University Cancer Center, University Medical Center Hamburg-Eppendorf, 20251 Hamburg, Germany.

Insights

Mebendazole (MBZ) effectively targets leukemia stem cells by inhibiting the Hedgehog (HH) pathway, offering a new strategy to overcome chemotherapy resistance in acute myeloid leukemia (AML). This study demonstrates MBZ

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • Elderly patients with acute myeloid leukemia (AML) face poor prognoses due to chemotherapy resistance.
  • Aberrant activation of GLI transcription factors in the Hedgehog (HH) pathway contributes to leukemic transformation.

Purpose of the Study:

  • To investigate the anti-leukemic effects of mebendazole (MBZ) in AML.
  • To explore MBZ's potential to overcome chemotherapy resistance by targeting the HH pathway.

Main Methods:

  • Assessed MBZ's anti-leukemic effects on AML cells in vitro.
  • Utilized luciferase reporter assays to measure GLI promoter activity.
  • Performed molecular dynamics simulations of the MBZ-HSP90 complex.
  • Analyzed MBZ treatment in two refractory AML patients.

Main Results:

  • MBZ demonstrated dose-dependent anti-leukemic effects and sensitized AML cells to cytarabine.
  • MBZ significantly reduced GLI1/GLI2 protein levels and GLI promoter activity.
  • MBZ induced proteasomal degradation of GLI transcription factors by inhibiting HSP70/90 chaperone activity.
  • Patient data showed MBZ reduced GLI signaling and blast counts in one case.

Conclusions:

  • MBZ acts as an effective GLI inhibitor by targeting HSP70/90 chaperone activity.
  • MBZ shows promise as an adjunct therapy to conventional chemotherapy for AML.
  • Further clinical evaluation of MBZ in combination therapy for AML is warranted.