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. 2022 Sep 26;13:5657. doi: 10.1038/s41467-022-33410-w

Fig. 2. GDYO showed anti-leukemia efficacy against DNMT3A mutant AML cells.

Fig. 2

a Cell viability assay of OCI-AML2 and OCI-AML3 treated with different carbon-based nanomaterials for 24 h. n = 3 biologically independent experiments. b Schematic illustration showing the structures of GDYO and GO. Carbon and oxygen atoms were shown in blue and red respectively. c C 1 s spectra of XPS scan for GDYO. d Cell viability assay of DNMT3A-mutant AML cell lines (OCI-AML2, OCI-AML3) and DNMT3A wildtype AML cell lines (HL-60, THP-1) treated with GO or GDYO at different concentrations for 24 h. n = 3 biologically independent experiments. e Apoptotic rates in OCI-AML3 and HL-60 treated with 20 μg/mL GO/GDYO for 48 h. n = 3 biologically independent experiments. f Cell adhesion assay on fibronectin for OCI-AML3 and HL-60 treated with 20 μg/mL GO/GDYO for 24 h. n = 3 biologically independent experiments. g Wright-Giemsa staining showing signs of maturation in GDYO-treated OCI-AML3. Scale bar, 20 μm. h–i Flow cytometry analysis of leukemic progenitor cells and leukemic stem cells in OCI-AML3 and HL-60 treated with 20 μg/mL GO/GDYO for 72 h. n = 3 biologically independent experiments. The data were shown as the mean ± SD. Statistical significance was tested with a two-tailed, unpaired Student’s t test. Source data are provided as a Source Data file.