Table 3

Inhibition of clonogenic growth of primary CML cells by SMA-ZnPP

Control medium
SMA-ZnPP
CFU-GMBFU-ECFU-GEMMCFU-GMBFU-ECFU-GEMM
CML (MNC) no. 1 29 133 
CML (MNC) no. 2 18 160 
CML (MNC) no. 3 17 59 
Healthy donor (MNC) no. 1 27 20 
Healthy donor (MNC) no. 2 36 15 
Healthy donor (MNC) no. 3 37 35 
Healthy donor (CD34+ cells) 43 110 31 106 
CML (CD34+ cells) no. 1 12 107 
CML (CD34+ cells) no. 2 21 210 
CML (CD34+ cells) no. 3 18 22 
Control medium
SMA-ZnPP
CFU-GMBFU-ECFU-GEMMCFU-GMBFU-ECFU-GEMM
CML (MNC) no. 1 29 133 
CML (MNC) no. 2 18 160 
CML (MNC) no. 3 17 59 
Healthy donor (MNC) no. 1 27 20 
Healthy donor (MNC) no. 2 36 15 
Healthy donor (MNC) no. 3 37 35 
Healthy donor (CD34+ cells) 43 110 31 106 
CML (CD34+ cells) no. 1 12 107 
CML (CD34+ cells) no. 2 21 210 
CML (CD34+ cells) no. 3 18 22 

Primary mononuclear cells (MNC) were isolated from the peripheral blood of untreated CML patients or from healthy controls by Ficoll density centrifugation and were then cultured in control medium or SMA-ZnPP (10 μM) for 24 hours. Thereafter, cells were cultured in methylcellulose in the presence of cytokines as described in the text for 14 days. Then, cultures were examined for the number of colonies by an inverted microscope. Results show the numbers of colonies per 105 cells (MNC seeded on day 0) or colonies per 5 x 103 CD34+ cells and represent the mean of duplicates in each donor.

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