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. Author manuscript; available in PMC: 2024 Sep 2.
Published in final edited form as: Toxicol Pathol. 2023 Apr 3;51(1-2):39–55. doi: 10.1177/01926233231157322

Table 3.

Summary of Kras and Egfr Mutations in Nontumor Lung Tissue and Alveolar/bronchiolar Adenomas and Carcinomas from Wistar Han Rats in the 2-Year Inhalation Study of Antimony Trioxidea

Tissue: Antimony Trioxide Mutation Frequencyb
Kras Codons
Egfr Exons
Concentration Kras Egfr 16 18 19 20 21

Nontumor lung: 0 mg/m3 0/11 (0) 0/11(0) 0 0 0 0 0
Lung tumors: 0 mg/m3 0/4 (0) 0/4 (0) 0 0 0 0 0
3 mg/m3 0/5 (0) 3c/5 (60) 0 2 2 0 1
10 mg/m3 1/11 (9) 6/11 (55) 1 2 2 1 1
30 mg/m3 0/10 (0) 4/10 (40) 0 0 1 2 1

All exposed groups combined 1/26 (4) 13c/26 (50) 1 4 5 3 3
 Without pulmonary overload 0/5 (0) 3c/5 (60) 0 2 2 0 1
 With pulmonary overload 1/21 (5) 10/21 (48) 1 2 3 3 2
a

Male and female Wistar Han rats were exposed to 0, 3, 10, or 30 mg/m3 antimony trioxide daily by inhalation for 2 years. Silent mutations are not included. There were no significant differences from the chamber control group by the one-sided Fisher’s exact test and no significant exposure-concentration trend by the Cochran-Armitage trend test.

b

Number of tissues with mutation/number of tissues assayed (% with mutation).

c

Same animal with double mutations (M246 with Egfr 19 and 21; M257 with Egfr 18 and 19).