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. 2011 May 12;11:39. doi: 10.1186/1472-6882-11-39

Table 2.

Expression of PPARγ, COX-2 and iNOS in human HCC cell lines

PPARγ expression COX-2 expression iNOS expression



IGF-1 L.obtusiloba extract IGF-1 and L.obtusiloba extract IGF-1 L.obtusiloba extract IGF-1 and L.obtusiloba extract IGF-1 L.obtusiloba extract IGF-1 and L.obtusiloba extract
HepG2 4.31 ± 0.51* 0.76 ± 0.14 1.15 ± 0.09# n.d. n.d. n.d. 1.17 ± 0.07 0.21 ± 0.14* 0.21 ± 0.09*;#
Hep3B 1.33 ± 0.12* 0.84 ± 0.09 0.81 ± 0.05# 2.28 ± 0.19* 0.77 ± 0.08* 1.09 ± 0.04*;# n.d. n.d. n.d.
Huh-7 1.17 ± 0.05 0.21 ± 0.10* 0.31 ± 0.12*;# n.d. n.d. n.d. n.d. n.d. n.d.
SK-Hep1 1.43 ± 0.11* 0.75 ± 0.09* 0.89 ± 0.07# 3.21 ± 0.34* 0.80 ± 0.07* 0.82 ± 0.09# 1.87 ± 0.12* 0.27 ± 0.12* 0.35 ± 0.06*;#

Cell lysates of HCC cell lines as described for Table 1, were subjected to specific western-blots for PPARγ, COX 2 and iNOS and for β actin as equal loading control. Densitometry of specific band intensity was normalized to β-actin expression. Mean values ± SD from three independent experiments. PPARγ, COX-2 and iNOS protein expression levels were calculated in relation to the respective untreated cells. Mean values ± SD from three independent experiments. *P < 0.05 compared to the untreated control, # P < 0.05 compared to IGF-1-treated cells, n.d. - not detected