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. Author manuscript; available in PMC: 2007 Nov 29.
Published in final edited form as: Toxicol Pathol. 2007;35(1):81–85. doi: 10.1080/01926230601063839

Table 2.

K-ras mutations in lung neoplasms from ethylene oxide-exposed B6C3F1 mice.

Codon 12 (GGT)
Codon 13 (GGC)
Codon 61 (CAA)
Treatment K-ras mutations (%) GAT TGT GTT CGT AGC CGC CGA CAT CAC
Controla 27/108 (25) 11b 5 1 0 0 3 2 4 1
Ethylene oxidec 23/23 (100)d 2 0 21 0 1 0 1 0 0
A/B adenoma 5/5 (100) 0 0 5 0 0 0 0 0 0
A/B carcinoma 18/18 (100) 2 0 16 0 1 0 1 0 0
50 ppm 8/8 (100) 0 0 8 0 0 0 0 0 0
100 ppm 15/15 (100) 2 0 13 0 1 0 1 0 0
a

Concurrent controls (8) combined with historical spontaneous lung neoplasms (100) from control B6C3F1 mice.

b

One mutation was from a concurrent control.

c

Male and female B6C3F1 mice were exposed to 0, 50, or 100 ppm ethylene oxide by inhalation 6 hours/day, 5 days/week for 2 years.

d

Two neoplasms had 2 mutations.