Mechanism of Resistance to the WDR5 Inhibitor in MLL-Rearranged Leukemia.
Lulu LiuLingling ShenZhilou DingMiao HeEn LiJohn A TallaricoRishi K JainHe WangPublished in: ACS chemical biology (2023)
Drug resistance is a major problem often limiting the long-term effectiveness of targeted cancer therapeutics. Resistance can be acquired through mutations or amplification of the primary drug targets or activation of bypass signaling pathways. Considering the multifaceted function of WDR5 in human malignancies, WDR5 has emerged as an attractive drug target for the discovery of small-molecule inhibitors. In this study, we investigated if cancer cells might develop resistance to a highly potent WDR5 inhibitor. We established a drug-adapted cancer cell line and discovered that WDR5 P173L mutation occurs in the resistant cells, which confers resistance by preventing target engagement of the inhibitor. This work elucidated the WDR5 inhibitor's potential resistance mechanism in a preclinical study as a reference for future study in the clinical stage.
Keyphrases
- small molecule
- acute myeloid leukemia
- endothelial cells
- randomized controlled trial
- bone marrow
- squamous cell carcinoma
- signaling pathway
- cell death
- stem cells
- systematic review
- cell proliferation
- protein protein
- epithelial mesenchymal transition
- drug delivery
- nucleic acid
- lymph node metastasis
- mass spectrometry
- pi k akt
- electronic health record