TABLE 1.
SL3-3 virus | Tumor incidence (no. of mice with tumor development/no. injected) | Mean tumor latency (no. of days ± SD) | Histopathologya | Clonal DNA rearrangementsb (no. of tumors with clonal rearrangements/no. investigated)
|
Complex enhancer changesc (no. of tumors with complex enhancer changes/no. examined) | |
---|---|---|---|---|---|---|
Igκe | TCRβ | |||||
wt | 13/13 | 60 ± 9 | Pre-TLLd | 0/11 | 11/11 | ND |
mEa/s | 24/24 | 58 ± 8 | ND | 0/11 | 11/11 | 0/24 |
3mGR | 21/21 | 57 ± 6 | Pre-TLL | 0/11 | 11/11 | 0/21 |
3mGR+mEa/s | 25/25 | 55 ± 9 | ND | 0/11 | 11/11 | 2/24 |
3mEgre | 23/23 | 109 ± 44 | Various types | 13/23 | ||
14/23 | 105 ± 35 | Pre-TLL | 0/14 | 14/14 | 12/14 | |
2/23 | 98 ± 0 | PCT/Pre-TLL | 2/2 | 2/2 | 0/2 | |
2/23 | 156 ± 55 | PCT | ND | ND | 0/2 | |
2/23 | 125 ± 134 | ML w.M | 0/2 | 0/2 | 0/2 | |
2/23 | 87 ± 16 | ML wo.M | 0/2 | 0/2 | 1/2 | |
1/23 | 111 | PCT/MKL | 1/1 | ND | 0/1 | |
3mEgre+mEa/s | 21/21 | 180 ± 41 | Various types | 12/21 | ||
9/21 | 213 ± 15 | PCT/STL | 9/9 | 9/9f | 5/9 | |
5/21 | 144 ± 41 | Pre-TLL | 3/5 | 4/5 | 3/5 | |
2/21 | 133 ± 18 | PCT/Pre-TLL | 1/2 | 2/2 | 1/1 | |
2/21 | 153 ± 49 | PCT | 2/2 | 1/2 | 1/2 | |
1/21 | 187 | ML | 1/1 | 1/1 | 0/1 | |
1/21 | 187 | PCT/ML wo.M | 1/1 | 0/1 | 1/1 | |
1/21 | 206 | PCT/ML | 0/1 | 0/1 | 0/1 |
Tumor phenotypes were determined by histopathological examination. ML w.M, myeloid leukemia with maturation; ML wo.M, myeloid leukemia without maturation; ML, myeloid leukemia, not otherwise specified; MKL, megakaryoblastic leukemia; PCT, plasmacytomas; pre-TLL, preT-cell lymphoblastic lymphoma; STL, small T-cell lymphoma; and ND, not determined. Some animals developed tumors of mixed phenotypes (data not shown).
Detected by the Southern blot analysis of HindIII-digested genomic tumor DNA with TCRβ (J1 and J2) and Igκ light chain-specific probes.
Complex secondary enhancer changes found in virus-induced tumors by PCR analysis.
Diagnosed for another series of mice injected with wt SL3-3 at the same facility.
All Igκ rearrangements were represented by very weak bands.
T-cell rearrangements observed in four of the nine cases were weak.