Copyright
©The Author(s) 2015.
World J Pharmacol. Jun 9, 2015; 4(2): 180-192
Published online Jun 9, 2015. doi: 10.5497/wjp.v4.i2.180
Published online Jun 9, 2015. doi: 10.5497/wjp.v4.i2.180
Figure 1 Simplified diagram of oncogenic targets in pancreatic cancer.
The binding of ligands (including VEGF, EGF, IGF-1 and HGF) to receptors activates signalling pathways including the PI3K-Akt and the Ras pathways affecting downstream targets such as mTOR and MAPK. VEGF: Vascular endothelial growth factor; EGF: Epidermal growth factor; IGF-1: Insulin growth like factor-1; HGF: Hepatocyte growth factor; PI3K: Phosphatidylinositide 3-kinases; mTOR: Mammalian target of rapamycin; RAS: Rat activated sarcoma; GDP: Guanosine diphosphate; GTP: Guanosine triphosphate; MAP: Mitogen activated kinase; CD: Cytoplasmic domain; PTC1: Patched; SMO: Smooth muscle, GL1.
- Citation: Thillai K, Sarker D, Ross P. Progress in pancreatic cancer therapeutics: The potential to exploit molecular targets. World J Pharmacol 2015; 4(2): 180-192
- URL: https://www.wjgnet.com/2220-3192/full/v4/i2/180.htm
- DOI: https://dx.doi.org/10.5497/wjp.v4.i2.180