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A combination of **SX-682** and **decitabine** is being investigated for the treatment of myelodysplastic syndromes (MDS). **SX-682** is a small molecule inhibitor targeting the chemokine receptors **CXCR1** and **CXCR2**, potentially reducing tumor-promoting inflammation and cellular migration. **Decitabine** is an FDA-approved DNA methylation inhibitor that acts as a hypomethylating agent by inhibiting **DNA methyltransferases**, leading to decreased DNA methylation and reactivation of tumor suppressor genes. This combination targets distinct pathogenic mechanisms in MDS, combining epigenetic modulation with chemokine receptor antagonism[1][2][5].
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