Genetic deletion of microsomal prostaglandin E synthase-1 suppresses mouse mammary tumor growth and angiogenesis

• Published in: Prostaglandins & other lipid mediators 2013-10, Vol.106, p.99-105
• Main Authors: Howe, Louise R., Subbaramaiah, Kotha, Kent, Claire V., Zhou, Xi K., Chang, Sung-Hee, Hla, Timothy, Jakobsson, Per-Johan, Hudis, Clifford A., Dannenberg, Andrew J.
• Format: Article
• Language: English
• Subjects: Angiogenesis; Animals; Aromatase; Aromatase - metabolism; Breast cancer; Carcinogenesis - genetics; Cell Line, Tumor; Cell Proliferation; Female; Gene Deletion; Gene Expression Regulation, Neoplastic; Humans; Intramolecular Oxidoreductases - deficiency; Intramolecular Oxidoreductases - genetics; Mammary Glands, Animal - metabolism; Mammary Neoplasms, Experimental - blood supply; Mammary Neoplasms, Experimental - enzymology; Mammary Neoplasms, Experimental - genetics; Mammary Neoplasms, Experimental - pathology; Medicin och hälsovetenskap; Mice; Mice, Transgenic; Microvessels - metabolism; Mouse; mPGES-1; Neovascularization, Pathologic - genetics; PGE2; Prostaglandin-E Synthases; Receptor, ErbB-2 - genetics; Vascular Endothelial Growth Factor A - metabolism
• ISSN: 1098-8823
• DOI: 10.1016/j.prostaglandins.2013.04.002

•Knocking out mPGES-1 suppresses mouse mammary tumor growth.•Angiogenesis is reduced by genetic ablation of mPGES-1.•Aromatase activity is substantially reduced in mPGES-1-deficient mammary glands. The cyclooxygenase/prostaglandin (COX/PG) signaling pathway is of central importance in inflammation and neoplasia. COX inhibitors are widely used for analgesia and also have demonstrated activity for cancer prophylaxis. However, cardiovascular toxicity associated with this drug class diminishes their clinical utility and motivates the development of safer approaches both for pain relief and cancer prevention. The terminal synthase microsomal PGE synthase-1 (mPGES-1) has attracted considerable attention as a potential target. Overexpression of mPGES-1 has been observed in both colorectal and breast cancers, and gene knockout and overexpression approaches have established a role for mPGES-1 in gastrointestinal carcinogenesis. Here we evaluate the contribution of mPGES-1 to mammary tumorigenesis using a gene knockout approach. Mice deficient in mPGES-1 were crossed with a strain in which breast cancer is driven by overexpression of human epidermal growth factor receptor 2 (HER2/neu). Loss of mPGES-1 was associated with a substantial reduction in intramammary PGE2 levels, aromatase activity, and angiogenesis in mammary glands from HER2/neu transgenic mice. Consistent with these findings, we observed a significant reduction in multiplicity of tumors ≥1mm in diameter, suggesting that mPGES-1 contributes to mammary tumor growth. Our data identify mPGES-1 as a potential anti-breast cancer target.