Table 2.

Effects of anti-bcr-abl siRNAs on colony formation of primary CML cells

Cell sample/siRNACFU-GMBFU-E
CML-PBMNCs   
 No. 1   
  GL2 15  
  b3a2_1 13  
 No. 2   
  GL2 45 64  
  b3a2_1 43 43  
 No. 3   
  GL2 2  
  b3a2_1 1  
 No. 4   
  GL2 23 53  
  b3a2_1 22 45 
CML-CD34+ cells   
 No. 5   
  GL2 30 17  
  b3a2_1 32 17  
  No STI571 29 14  
  1 μM STI571 2  
 No. 5   
  GL2 139 62  
  b3a2_1 132 68  
 No. 6   
  GL2 128 72  
  b3a2_1 88 66 
Cell sample/siRNACFU-GMBFU-E
CML-PBMNCs   
 No. 1   
  GL2 15  
  b3a2_1 13  
 No. 2   
  GL2 45 64  
  b3a2_1 43 43  
 No. 3   
  GL2 2  
  b3a2_1 1  
 No. 4   
  GL2 23 53  
  b3a2_1 22 45 
CML-CD34+ cells   
 No. 5   
  GL2 30 17  
  b3a2_1 32 17  
  No STI571 29 14  
  1 μM STI571 2  
 No. 5   
  GL2 139 62  
  b3a2_1 132 68  
 No. 6   
  GL2 128 72  
  b3a2_1 88 66 

Standard colony assays were performed with PBMNCs (patient samples 1-4) after electroporation with the respective siRNA. Purified CD34+ cells from patient sample 5 were initially cultured in standard colony assays, and the samples “No STI571” and “1 μM STI571” were not electroporated. The last 4 lanes show CD34+ cells (patient samples 5, 6) first grown in suspension culture for 3 days and then plated into standard colony assays. No viable cells were found after suspension culture in the presence of 1 μM STI571 after 3 days (patient sample 5).

CFU-GM indicates colony-forming unit granulocyte macrophage; and BFU-E, burst-forming unit erythroid.

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