It has been published that ORs in cancer when activated, can increase the Ca2+ concentration in the cytosol [92], phosphorylate p38 and Erk1/2 MAPK [21], stimulate the cAMP/PKA pathway and EGFR and AKT signaling cascades, and increase cell proliferation, angiogenesis, cell cycle arrest, cell survival, and apoptosis [71,79,93]. The gene discussed is EGFR; the disease is cancer.