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Table 1 Summary of soft agar colony formation assay and xenograft propagation experiment: NHA and NIH3T3 cells infected with retroviral vectors expressing hTERT (T), SV40ER (S), H-RasV12 (R), myrAKT (A), and/or MGMT as well as parental NHA cells were subjected to the soft-agar colony formation and xenograft propagation assays.

From: O6-methylguanine-DNA methyltransferase is downregulated in transformed astrocyte cells: implications for anti-glioma therapies

Cell types

Colony numbers a

% Tumor incidence (n) b

NHA (parental)

0

ND

NHA/TS

0

0 (3)

NHA/TSR

664 ± 19

100 (3)

NHA/TSRA

736 ± 51

100 (3)

NHA/TSR + MGMT

649 ± 34

ND

NIH3T3/R

1440 ± 56

ND

NIH3T3/R + MGMT

1344 ± 88

ND

  1. aNHA (2 × 104) and NIH3T3 cells (1 × 104) were plated in soft-agar (0.36% top agar containing 5% fetal calf serum in 60-mm dishes) and incubated for 21 days and 14 days, respectively. Colonies were stained with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide, and the numbers of stained colonies were counted. Results represent mean ± SD from two independent triplicate experiments.
  2. b3 × 106 cells were injected s.c. into nude mice. n, number of animals treated. ND, not done.