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. 2018 Jan 16;115(5):1045–1050. doi: 10.1073/pnas.1715930115

Fig. 1.

Fig. 1.

Effect of IGF1 and insulin on TXNIP gene expression. (A) Total RNA was obtained from individual LS and control lymphoblastoid cell lines and TXNIP mRNA levels were measured by RT-QPCR. The bars represent the mean ± SEM of three individual cell lines. **P < 0.01, significantly different versus controls. P69 (B) and M12 (C) prostate cells were deprived of serum for 24 h and then exposed to IGF1 (50 ng/mL, gray bars) or insulin (clear bars) for 1, 3, or 5 h. At the end of the incubation, cells were harvested and levels of TXNIP mRNA were measured by RT-QPCR. The bars represent the mean ± SEM of three independent experiments, each performed in triplicate. *P < 0.01 relative to serum-deprived conditions. A value of 1 was given to TXNIP mRNA levels in control cells (solid bars).