In addition, a global RNA microarray analysis of GIP administrated to MCF-7 breast cancer cell cultures for 8 days demonstrated that GIP was capable of the up- and/or down-regulation of the RNA of multiple outward/inward flux cation channel proteins resulting in cation channel regulation and cell cycle arrest in breast cancer cell cultures [5] (Table 1, Part I and Part II). The gene discussed is GIP; the disease is breast carcinoma.