Malic Enzyme 1 (ME1) is pro-oncogenic in Apc Min/+ mice

• Published in: Scientific reports Vol. 8; no. 1; p. 14268
• Main Authors: Fernandes, Lorenzo M, Al-Dwairi, Ahmed, Simmen, Rosalia C M, Marji, Meera, Brown, Dustin M, Jewell, Sarah W, Simmen, Frank A
• Format: Journal Article
• Language: English
• Published: England 24.09.2018
• Subjects: Adenomatous Polyposis Coli Protein - genetics; Animals; Carcinogenesis - genetics; Cell Proliferation - genetics; Colonic Neoplasms - genetics; Colonic Neoplasms - pathology; DNA-Binding Proteins - genetics; Epithelial Cells - metabolism; Epithelial Cells - pathology; Gastrointestinal Tract - metabolism; Gastrointestinal Tract - pathology; Gene Expression Regulation, Neoplastic - genetics; Humans; Intestinal Mucosa; Malate Dehydrogenase - antagonists & inhibitors; Malate Dehydrogenase - genetics; Mice; Oncogenes; Rats; Transcription Factors - genetics
• ISSN: 2045-2322

Cytosolic Malic Enzyme (ME1) provides reduced NADP for anabolism and maintenance of redox status. To examine the role of ME1 in tumor genesis of the gastrointestinal tract, we crossed mice having augmented intestinal epithelial expression of ME1 (ME1-Tg mice) with Apc mice to obtain male Apc /ME1-Tg mice. ME1 protein levels were significantly greater within gut epithelium and adenomas of male Apc /ME1-Tg than Apc mice. Male Apc /ME1-Tg mice had larger and greater numbers of adenomas in the small intestine (jejunum and ileum) than male Apc mice. Male Apc /ME1-Tg mice exhibited greater small intestine crypt depth and villus length in non-adenoma regions, correspondent with increased KLF9 protein abundance in crypts and lamina propria. Small intestines of male Apc /ME1-Tg mice also had enhanced levels of Sp5 mRNA, suggesting Wnt/β-catenin pathway activation. A small molecule inhibitor of ME1 suppressed growth of human CRC cells in vitro, but had little effect on normal rat intestinal epithelial cells. Targeting of ME1 may add to the armentarium of therapies for cancers of the gastrointestinal tract.