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Editorials
A new kid on the block for acute myeloid leukemia treatment? Homoharringtonine interferes with key pathways in acute myeloid leukemia cells
Stefan K. Bohlander
Marijana Kumerich Chair in Leukaemia and Lymphoma Research, Leukaemia and Blood Cancer Research Unit, Department of Molecular Medicine and Pathology, The University of Auckland, Auckland, New Zealand
E-mail: STEFAN K. BOHLANDER - s.bohlander@auckland.ac.nz doi:10.3324/haematol.2019.234880
Treatment for acute myeloid leukemia (AML) has not changed substantially in the past 40 years. We still largely rely on the substances (antimetabolites and topoisomerase inhibitors) that were introduced for AML treatment in the 1970s. Although treatment out- comes for AML, other than acute promyelocytic leukemia (APM), have improved over the years, these improvements have been slow and incremental and been largely achieved by optimizing dosing schedules and bet- ter supportive care.1 However, substantial improvements in treatment, with high cure rates, have been achieved in genetically well defined subgroups of leukemia like acute promyelocytic leukemia (driven by the PML/RARA fusion)2 and chronic myeloid leukemia (driven by the BCR/ABL fusion).3 AML, however, is a different beast. It is not a single disease but a genetically highly heteroge- neous group of malignant diseases of the hematopoietic stem cell that have similar phenotypes. The great genetic heterogeneity of AML, which was recognizable even in the early cytogenetic studies, has become very apparent with the advent of next-generation sequencing which has allowed the analysis of AML genomes at base pair reso- lution.4,5
Considering that AML is a highly heterogeneous group of malignant diseases, it is not surprising that a 'one size fits all' standard treatment approach can not achieve sat- isfactory cure rates. One critical question is: how het- erogenous is AML? How many different diseases are we dealing with? If we simply looked at the number of genes that have been shown to harbor somatic mutation in AML and the number of somatic mutations in each AML sample, the number of potential combinations, and thus AML subgroups, would be astronomical. However, this is most likely an overestimate of the heterogeneity and complexity of AML, and there is likely only a much smaller number of crucial pathways that are disrupted in AML pathogenesis. Identifying and targeting these cru- cial pathways should greatly improve AML therapy.
In their report in this issue of the Journal, Chen et al. present convincing evidence that homoharringtonine (HHT) (omacetaxine mepesuccinate), an alkaloid found in the Hainan plum yew,6 is targeting such a critical path- way in AML pathogenesis.7 HHT has been used in China for several years for the treatment of AML8,9 and was approved in 2012 by the US Food and Drug Administration (FDA) for the treatment of chronic myeloid leukemia (CML) with resistance to tyrosine kinase inhibitors.10 The mode of action of HHT in CML was reported to be through the inhibition of protein syn- thesis by binding to the A site of the ribosome.11
Building on the success of HHT in the treatment of AML patients in China, where a remission rate of 83%
was achieved when HHT was used in combination with cytarabine and aclarubicin to treat de novo AML patients,9 Chen et al. explored the mechanism of HHT efficacy in murine and human AML cell lines as well as in murine and xenotransplant AML models. HHT treatment led to apoptosis and differentiation in cell lines and resulted in increased survival in murine AML transplantation models and in human AML xenograft models. Then the group set out to elucidate the molecular mechanism responsible for the observed effects of HHT treatment.
In a series of elegant experiments, Chen et al. showed that HHT binds to the transcription factor SP1, thereby inhibiting the binding of SP1 to its cognate DNA sequences. However, the route to this discovery was not straightforward. Initially, the group examined global 5- hydroxymethylcytosine (5hmC) levels in cells treated with HHT and noticed a remarkable reduction in global 5hmC levels. 5hmC is generated by the oxidation of methylcytosine groups in DNA through the action of the three dioxygenase enzymes TET1, 2 and 3.12 As only the expression of the TET1 gene, and not of TET2 or TET3, was significantly down-regulated after HHT treatment, the authors concluded that the reduction in TET1 expres- sion, and hence a reduced TET1 enzymatic activity, was probably the cause of the reduced 5hmC levels. Examining the promoter region of TET1, they found mul- tiple binding motifs for the transcription factor SP1 and reasoned that SP1 might be important for the HHT- induced downregulation of TET1 expression. And indeed, they could show that HHT treatment reduced binding of SP1 to its binding motifs in the TET1 promoter region. Furthermore, a drug affinity responsive target sta- bility assay and a cellular thermal shift assay provided strong evidence that HHT is indeed binding to the SP1 protein and preventing SP1 from binding to its recogni- tion sites in the TET1 promoter region.
What are the consequences of the HHT-induced reduc- tion in TET1 transcription and, consequently, the global reduction in 5hmC levels? The 5hmC mark is associated with active transcription. Thus, the reduction in 5hmC levels was accompanied by a genome-wide reduction in gene transcription. More than 1,600 genes showed reduced expression. Very interestingly, one of the most strongly repressed genes was FLT3, which codes for the tyrosine kinase receptor FLT3. The authors confirmed that the FLT3 gene was one of the direct targets of TET1 action with chromatin immunoprecipiation-quantitative polymerase chain reaction (ChIP-qPCR). FLT3 signaling is critical in the maintenance of the leukemic phenotype and activates a number of genes, including HOXA9 and MEIS1, which are highly expressed in hematopoietic stem and progenitor cells. There is a positive feed-back
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