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. 2008 Apr 8;41(3):532–553. doi: 10.1111/j.1365-2184.2008.00528.x

Table 2.

Effects of pre‐treatments with individual PBPs 1–5, PBP‐mix and EGCG on latency period, multiplicity and incidence of DMBA‐initiated and TPA‐promoted mouse skin carcinogenesis

Group No. (as per Table 1a) Treatment Latency (in weeks) Multiplicity Time points (in weeks) Incidence (%) Time points (in weeks)
10 20 30 40 10 20 30 40
2 Acetone + TPA 11 ± 0.28 0.41 ± 0.001 4.00 ± 0.01 8.24 ± 0.09 12.00 ± 0.1 13 100 100 100
10  PBP1 + TPA 17 ± 1.72 0.05 ± 0.002* 0.91 ± 0.05* 1.90 ± 0.01  4.20 ± 0.04*  6  58*  76 100
11  PBP2 + TPA 14 ± 1.58* 0.00* 0.35 ± 0.001* 1.00 ± 0.05*  2.90 ± 0.05  0  31*  63*  69*
12  PBP3 + TPA 18 ± 1.01* 0.00* 0.59 ± 0.002* 2.50 ± 0.04*  4.21 ± 0.04*  0  38* 100 100
13  PBP4 + TPA 15 ± 1.44* 0.05 ± 0.001 1.42 ± 0.01 3.90 ± 0.04*  5.59 ± 0.04*  6  70 100 100
14  PBP5 + TPA 11 ± 1.21 0.39 ± 0.003 2.00 ± 0.05 4.10 ± 0.05*  7.01 ± 0.1 13  95 100 100
15 PBPmix + TPA 20 ± 1.58* 0.00* 0.81 ± 0.02 3.20 ± 0.02*  4.90 ± 0.09  0 100 100 100
16 EGCG + TPA 19 ± 1.92 0.00* 1.19 ± 0.004* 3.80 ± 0.02  5.20 ± 0.09  0  72 100 100

Mean ± SE; n = 10 mice per group.

*

P < 0.01 compared to group no. 2 – acetone + TPA‐treated, anova with Tukey's test for latency and multiplicity and Fisher's exact test for incidence.