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. 2016 Sep 22;9:93. doi: 10.1186/s13045-016-0327-5

Fig. 3.

Fig. 3

Alantolactone selectively induced apoptosis of LSCs in primary AML cells. a Alantolactone induced the apoptosis of CD34+CD38 cells with a dose-dependent manner in primary AML cells from AML specimens after treatment of alantolactone for 18 h. Each point represents an AML specimen. b Alantolactone reduced the percentage of CD34+CD38 cells with a dose-dependent manner in primary AML cells after the treatment of alantolactone for 18 h. Each point represents an AML specimen. c Alantolactone selectively induced apoptosis of CD34+CD38 cells comparing with total cells in primary AML cells after the treatment of alantolactone for 18 h by flow cytometry. d Ara-C showed negligible cytotoxicity to CD34+CD38 and total cells in primary AML cells at the concentrations of 5 and 10 μM. e Alantolactone induced apoptosis of CD34+CD38 cells in primary AML cells by flow cytometry at the concentrations of 2.5, 5, and 10 μM. f Ara-C showed almost no effect on inducing apoptosis of CD34+CD38 cells in primary AML cells at the concentrations of 5 and 10 μM. g Alantolactone treatment demonstrated significantly less effect on inducing apoptosis of CD34+CD38 cells in normal hematopoietic cells comparing to that in primary AML cells at a concentration of 10 μM. *P < 0.05, **P < 0.01, ***P < 0.0001