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. Author manuscript; available in PMC: 2017 Aug 29.
Published in final edited form as: Amino Acids. 2011 Dec 21;43(3):1157–1169. doi: 10.1007/s00726-011-1171-0

Table 4. Genes significantly changed by acute nicotine treatment as confirmed by real-time PCR.

Gene symbol Gene Ratio ± SDa p value FDRb
DUSP Dual specificity phosphatase 2 1.23 ± 0.04 0.005 0.025
IL6ST Interleukin 6 signal transducer 0.81 ± 0.04 0.013 0.028
TRAF6 Tnf receptor-associated factor 6 0.90 ± 0.01 0.027 0.035
TGFBR2 Transforming growth factor, beta receptor 2 0.73 ± 0.07 0.009 0.028
ITGB1 Integrin beta 1 0.73 ± 0.10 0.004 0.025
HMGN1 High mobility group nucleosomal binding domain 1 1.37 ± 0.07 0.028 0.035
DAXX Fas death domain-associated protein 1.12 ± 0.06 0.023 0.035
MAPK14 Mitogen-activated protein kinase 14 1.14 ± 0.05 0.014 0.028
a

The ratio shown in this column is between gene expression in the nicotine-treated and control groups. For the ten genes verified by real-time PCR, the expression of eight is significantly (p < 0.05) different in response to acute nicotine treatment. For the other two genes, i.e., ARAF1 and RPS6KB1, the p value is 0.197 and 0.519, respectively. Although the expression change of the two genes did not reach significance, they showed a trend in the same direction as that detected with the microarray approach

b

FDR is calculated from the p values of the ten genes verified by real-time PCR via the method of Benjamini and Hochberg (1995). For ARAF1 and RPS6KB1, the FDR is 0.219 and 0.519, respectively; the values are not shown in the table, because the expression difference in the two genes was not significant in real-time PCR tests