The DNA Methyltransferase Inhibitor 5-Aza-4'-thio-2'-Deoxycytidine Induces C>G Transversions and Acute Lymphoid Leukemia Development.
Ryan M BertoliYang Jo ChungMichael J DifilippantonioAnthony WokaschMadison R B MarascoHaley L KlimaszewskiSusannah GammellYuelin Jack ZhuRobert L WalkerDengchao CaoAjay KhannaMatthew J WalterJames H DoroshowPaul S MeltzerPeter D AplanPublished in: Cancer research (2024)
DNA methyltransferase inhibitors (DNMTi), most commonly cytidine analogs, are compounds that decrease 5'-cytosine methylation. DNMTi are used clinically based on the hypothesis that cytosine demethylation will lead to re-expression of tumor suppressor genes. 5-Aza-4'-thio-2'-deoxycytidine (Aza-TdCyd or ATC) is a recently described thiol-substituted DNMTi that has been shown to have anti-tumor activity in solid tumor models. In this study, we investigated the therapeutic potential of ATC in a murine transplantation model of myelodysplastic syndrome. ATC treatment led to the transformation of transplanted wild-type bone marrow nucleated cells into lymphoid leukemia, and healthy mice treated with ATC also developed lymphoid leukemia. Whole-exome sequencing revealed 1,000 acquired mutations, almost all of which were C>G transversions in a specific 5'-NCG-3' context. These mutations involved dozens of genes involved in human lymphoid leukemia, such as Notch1, Pten, Pax5, Trp53, and Nf1. Human cells treated in vitro with ATC showed 1,000 acquired C>G transversions in a similar context. Deletion of Dck, the rate-limiting enzyme for the cytidine salvage pathway, eliminated C>G transversions. Taken together, these findings demonstrate a highly penetrant mutagenic and leukemogenic phenotype associated with ATC. Significance: Treatment with a DNA methyltransferase inhibitor generates a distinct mutation signature and triggers leukemic transformation, which has important implications for the research and clinical applications of these inhibitors.
Keyphrases
- bone marrow
- acute myeloid leukemia
- wild type
- cell proliferation
- induced apoptosis
- circulating tumor
- poor prognosis
- signaling pathway
- mesenchymal stem cells
- genome wide
- molecular docking
- gene expression
- combination therapy
- immune response
- liver failure
- single cell
- nucleic acid
- pi k akt
- lps induced
- adipose tissue
- cord blood
- high resolution
- binding protein
- endoplasmic reticulum stress
- nuclear factor
- circulating tumor cells
- toll like receptor
- transcription factor