Acute myeloid leukemia (AML) is a
hematologic malignancy that is
characterized by clonal proliferation of myeloid blasts. Despite the
progress that has been made in the treatment of various malignant
hematopoietic diseases, the effective treatment of AML remains very
challenging. Differentiation therapy has emerged as a promising approach
for leukemia treatment, and new and effective chemical agents to trigger
the differentiation of AML cells, especially drug-resistant cells,
are urgently required. Herein, the natural product jungermannenone
C, a tetracyclic diterpenoid isolated from liverworts, is reported
to induce cell differentiation in AML cells. Interestingly, the unnatural
enantiomer of jungermannenone C (1) was found to be more
potent than jungermannenone C in inducing cell differentiation. Furthermore,
compound 1 targets peroxiredoxins I and II by selectively
binding to the conserved cysteine residues and leads to cellular reactive
oxygen species accumulation. Accordingly, ent-jungermannenone
C (1) shows potential for further investigation as an
effective differentiation therapy against AML.