Copyright
©2012 Baishideng Publishing Group Co.
World J Gastroenterol. Apr 21, 2012; 18(15): 1781-1788
Published online Apr 21, 2012. doi: 10.3748/wjg.v18.i15.1781
Published online Apr 21, 2012. doi: 10.3748/wjg.v18.i15.1781
Figure 4 Effect of glyceraldehyde-derived advanced glycation end-products on the angiogenesis of hepatocellular carcinoma cells.
A and B: Hep3B and HepG2 cells were incubated with control unglycated bovine serum albumin (BSA) or glyceraldehyde-derived advanced glycation end-products (Glycer-AGEs) for 24 h. Vascular endothelial growth factor (VEGF) mRNA expression was analyzed using real-time reverse transcription-polymerase chain reactions, and results were normalized to the β-actin mRNA level; C and D: Hep3B and HepG2 cells were incubated with control unglycated BSA or Glycer-AGEs for 24 or 48 h. The conditioned medium was collected, and VEGF expression levels of the cells were determined by enzyme-linked immunosorbent assay. The open and filled bars represent results for cells treated with control unglycated BSA and Glycer-AGEs, respectively. Data are shown as the mean ± SD (n = 3), bP < 0.01 vs control unglycated BSA.
- Citation: Takino J, Yamagishi S, Takeuchi M. Glycer-AGEs-RAGE signaling enhances the angiogenic potential of hepatocellular carcinoma by upregulating VEGF expression. World J Gastroenterol 2012; 18(15): 1781-1788
- URL: https://www.wjgnet.com/1007-9327/full/v18/i15/1781.htm
- DOI: https://dx.doi.org/10.3748/wjg.v18.i15.1781