Next we tested whether selenium levels modulate AP-1 activity, VEGF, and IL-8 also in the animal organism and affect growth of early tumor stages. Because the IL-8 gene is not conserved in rats, its analog CXCL1 was investigated. The Solt-Farber model of rat hepatocarcinogenesis was used with and without selenium supplementation. Selenium supplementation increased serum selenium levels (Table 1). In the promotion phase, cell proliferation as well as volume of preneoplastic liver nodules were reduced from 38% to 14% volume fraction in the selenium-supplemented rats.25 Hepatic mRNA expression of VEGF and c-fos was reduced in the

promotion but not in the progression phase (Table 1). Nuclear translocation of selleck chemical c-jun and expression of CXCL1 were not influenced by selenium (Table 1). Serum VEGF and CXCL1 proteins were below the detection limit of commercially available ELISAs. Thus, in this rat model selenium supplementation decreases VEGF and c-fos expression as shown above in vitro; this effect is associated with a dramatic reduction of nodule growth.

Finally, we analyzed the effects of selenium and LOOH on growth factors and tumor GW-572016 ic50 size in patients with HCC. LOOH-Ab in blood plasma were determined similar to work published previously.33-35 Interestingly, LOOH-Ab levels were significantly higher in HCC patients than in healthy controls (Fig. 上海皓元 5A), suggesting higher amounts of circulating LOOH. Selenium levels inversely correlated with VEGF and IL-8

and also with tumor size in HCC patients, the latter only in those with tumors diameters up to 3 cm (Table 2; Fig. 5B). LOOH-Ab levels correlated positively with VEGF (only in patients with HCC <3 cm) and IL-8 and also with nuclear localization of c-jun indicating AP-1 activation (Table 2; Fig. 5C,D). These correlations in HCC patients are consistent with the above finding that LOOH enhances VEGF and IL-8 expression and AP-1 activation in cultured HCC cells, and that selenium antagonizes these effects. Finally, we reevaluated published gene expression data from HCC tissue of 60 patients.24 GPx4 but not GPx2 inversely correlated with VEGF and c-fos expression. GPx correlations with IL-8 and c-jun expression were not statistically significant, but VEGF positively correlated with IL-8 (Supporting Table 5). These data agree with the inhibitory role of the selenium-inducible GPx4 on VEGF expression in HCC cells found in vitro (see above). Inflammation and associated formation of ROS are widely accepted risk factors in hepatocarcinogenesis but important mechanistic details are still unknown. Here we report that peroxides of linoleic acid (LOOH) can activate the transcription factor AP-1, a sensor of oxidative stress36-38 and important promoter of hepatocarcinogenesis.