Table 2.

Tumorigenicity of mouse primary bone marrow cells expressing distinct Bcr-Abl proteins

Bcr-Abl Form Incidence*Latency (d) Tumor Mass (g)
p185 (No 85)2-153,2-155 5/5  21  4.5 ± 0.7  
p185 (No 103)2-153,2-155 4/4   21 5.4 ± 0.3  
p210 (No 102)2-155 0/5  150  0  
p210 (No 106)2-155 0/4  130  0  
p230 (No 83)2-155 0/5  160 0  
p230 (No 97)2-155,2-154 0/8  105-127  0  
p230 (No 105)2-155 0/4  130  
Bcr-Abl Form Incidence*Latency (d) Tumor Mass (g)
p185 (No 85)2-153,2-155 5/5  21  4.5 ± 0.7  
p185 (No 103)2-153,2-155 4/4   21 5.4 ± 0.3  
p210 (No 102)2-155 0/5  150  0  
p210 (No 106)2-155 0/4  130  0  
p230 (No 83)2-155 0/5  160 0  
p230 (No 97)2-155,2-154 0/8  105-127  0  
p230 (No 105)2-155 0/4  130  
*

Number of mice with tumors/total number of mice injected.

Time in days when tumors were first observed (p185) or time at which animals without tumors were killed (p210 and p230).

Mean mass of tumors ± 1 SD.

F2-153

All mice injected with p185 Bcr-Abl–expressing primary mouse bone marrow cells developed elevated white blood counts and splenomegaly with circulating GFP-positive lymphoid precursors consistent with the development of lymphoid leukemia.

F2-155

Indicates independently derived primary mouse bone marrow cultures.

F2-154

Five mice in this set died on days 105 to 128 but were free of tumor. The remaining 3 mice from this set were killed between days 121 and 127 and were also free from tumor; however, 2 of these mice had elevated white blood counts, splenomegaly, and polycythemia with circulating GFP-positive myeloid cells consistent with the development of a myeloid leukemia.

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