Period 2 Mutation Accelerates ApcMin/+ Tumorigenesis

• Published in: Molecular cancer research Vol. 6; no. 11; pp. 1786 - 1793
• Main Authors: Wood, Patricia A, Yang, Xiaoming, Taber, Andrew, Oh, Eun-Young, Ansell, Christine, Ayers, Stacy E, Al-Assaad, Ziad, Carnevale, Kevin, Berger, Franklin G, Peña, Maria Marjorette O, Hrushesky, William J M
• Format: Journal Article
• Language: English
• Published: United States American Association for Cancer Research 01.11.2008
• Subjects: Animals; Apc; beta Catenin - genetics; beta Catenin - metabolism; Cell Cycle Proteins - genetics; Cell Cycle Proteins - metabolism; Cell Line, Tumor; Cell Proliferation; circadian clock; Circadian Rhythm; Colon - pathology; Colonic Neoplasms - genetics; Colonic Neoplasms - pathology; Colonic Polyps - pathology; colorectal cancer; Cyclin D; Cyclins - metabolism; Disease Models, Animal; Down-Regulation; Genes, APC; Humans; Intestinal Mucosa - pathology; Intestinal Polyps - pathology; Mice; Mutation; Neoplasm Invasiveness - genetics; Nuclear Proteins - genetics; Nuclear Proteins - metabolism; Per2; Period Circadian Proteins; RNA Interference; Transcription Factors - genetics; Transcription Factors - metabolism; β-catenin
• ISSN: 1541-7786; 1557-3125
• DOI: 10.1158/1541-7786.MCR-08-0196

Colorectal cancer risk is increased in shift workers with presumed circadian disruption. Intestinal epithelial cell proliferation is gated throughout each day by the circadian clock. Period 2 ( Per2 ) is a key circadian clock gene. Per2 mutant ( Per2 m/m ) mice show an increase in lymphomas and deregulated expression of cyclin D and c-Myc genes that are key to proliferation control. We asked whether Per2 clock gene inactivation would accelerate intestinal and colonic tumorigenesis. The effects of PER2 on cell proliferation and β-catenin were studied in colon cancer cell lines by its down-regulation following RNA interference. The effects of Per2 inactivation in vivo on β-catenin and on intestinal and colonic polyp formation were studied in mice with Per2 mutation alone and in combination with an Apc mutation using polyp-prone Apc Min/+ mice. Down-regulation of PER2 in colon cell lines (HCT116 and SW480) increases β-catenin, cyclin D, and cell proliferation. Down-regulation of β-catenin along with Per2 blocks the increase in cyclin D and cell proliferation. Per2 m/m mice develop colonic polyps and show an increase in small intestinal mucosa β-catenin and cyclin D protein levels compared with wild-type mice. Apc Min/+ Per2 m/m mice develop twice the number of small intestinal and colonic polyps, with more severe anemia and splenomegaly, compared with Apc Min/+ mice. These data suggest that Per2 gene product suppresses tumorigenesis in the small intestine and colon by down-regulation of β-catenin and β-catenin target genes, and this circadian core clock gene may represent a novel target for colorectal cancer prevention and control. (Mol Cancer Res 2008;6(11):1786–93)