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. Author manuscript; available in PMC: 2011 Jun 1.
Published in final edited form as: Cancer Prev Res (Phila). 2010 Jun 1;3(6):707–717. doi: 10.1158/1940-6207.CAPR-09-0162

TABLE 2.

Gene expression analyses by quantitative real-time PCR

3 weeks 8 weeks 20 weeks

Gene P value FDR Fold-change P value FDR Fold-change P value FDR Fold-change
Cyp1b1 2.16E-03 4.33E-03 22.58 2.16E-03 2.89E-03 22.58 2.16E-03 3.46E-03 19.05
Cry1 2.16E-03 4.33E-03 4.30 2.16E-03 2.89E-03 2.79 2.16E-03 3.46E-03 2.94
Cbr3 2.16E-03 4.33E-03 3.56 2.16E-03 2.89E-03 2.55 2.16E-03 3.46E-03 2.79
Ces3 6.49E-02 6.49E-02 2.38 8.66E-03 9.89E-03 1.68 4.11E-02 4.70E-02 1.57
Tef 2.16E-03 4.33E-03 2.53 6.49E-02 6.49E-02 1.54 4.33E-03 5.77E-03 1.87
Ugt1a6a 6.49E-02 6.49E-02 1.71 2.16E-03 2.89E-03 2.58 6.49E-02 6.49E-02 1.46
Col3a1 1.52E-02 2.42E-02 0.54 2.16E-03 2.89E-03 0.30 2.16E-03 3.46E-03 0.38
Hdc 6.49E-02 6.49E-02 0.91 2.16E-03 2.89E-03 0.43 2.16E-03 3.46E-03 0.43

Total RNA was assayed by RT-PCR. Samples were analyzed in quadruplicate, and the resulting data were expressed as the average cycle threshold (Ct). The housekeeping gene Hprt1 was used for data normalization (ΔCt). Comparisons between control and smoke-exposed samples for statistical significance were determined using the Mann-Whitney test (P-value) and the step-up method of Benjamini & Hochberg (False Discovery Rate (FDR)). Fold-change was calculated using the Comparative Ct method (ΔΔCt). Genes induced or repressed following smoke exposure are indicated by a fold-change >1 or <1, respectively.