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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: Cancer Prev Res (Phila). 2011 Oct 25;4(11):1752–1760. doi: 10.1158/1940-6207.CAPR-11-0366

Table 4.

Histopathological analysis of tumors in A/J mice receiving NNK with or without nicotinea

Group Treatment Incidence (percent of mice) Multiplicity (Average per Mouse ± SD)

Adenoma Adenoma with dysplasia Carcinoma Adenoma Adenoma with dysplasia Carcinoma
1 (n=14) No nicotine/saline 7 7 0 0.07 ± 0.27 0.07 ± 0.27 0.0
2 (n = 15) Nicotine 0–46 weeks/saline 8 0 15 0.08 ± 0.28 0.0 0.15 ± 0.40
3 (n= 18) No nicotine/NNK 83 56 28 3.4 ± 2.4 0.83 ± 0.92 0.44 ± 0.78
4 (n = 18) Nicotine 0–46 weeks/NNK 89 61 44 4.4 ± 2.7 1.0 ± 1.1 0.67 ± 0.91
5 (n = 19) Nicotine 0–2 weeks/NNK 95 63 28 4.8 ± 3.5 1.0 ± 0.94 0.37 ± 0.68
6 (n = 20) Nicotine 2–46 weeks/NNK 85 65 50 4.4 ± 2.6 0.8 ± 0.70 0.70 ± 0.80
a

Treatments were as described in Fig. 1 and Table 3. Histological analysis was not carried out on lungs from 5 mice in Groups 1 and 2. Premature deaths occurred in Groups 2–5 as follows: Group 2, one death, week 3, cause of death – unknown, no microscopic analysis of tissues; Group 3, one death week 5 cause of death – unknown and one death at week 29 cause of death – disseminated lymphoma, pulmonary adenomas present; Group 4, one death week 43 cause of death – respiratory distress, adenocarcinoma with multifocal pulmonary adenomas, bronchiolar epithelial hyperplasia, alveolar histiocytosis and hemorrhage and one death at week 37 after NNK injection. Cause of death – dorsal skin tumor (a large non-malignant hematoma) pulmonary adenomas present; Group 5, one death at week 11 euthanized due to “labored breathing” no microscopic analysis of tissues.