The Circadian Clock Gene, Bmal1, Regulates Intestinal Stem Cell Signaling and Represses Tumor Initiation
Document Type
Article
Publication Date
1-1-2021
Publication Title
Cellular and Molecular Gastroenterology and Hepatology
Volume
12
Issue
5
First Page
1847
Keywords
Circadian Rhythms, Colorectal Cancer, Hippo Pathway, Intestinal Stem Cells
Last Page
1872.e0
Abstract
Background & Aims: Circadian rhythms are daily physiological oscillations driven by the circadian clock: a 24-hour transcriptional timekeeper that regulates hormones, inflammation, and metabolism. Circadian rhythms are known to be important for health, but whether their loss contributes to colorectal cancer is not known. We tested the nonredundant clock gene Bmal1 in intestinal homeostasis and tumorigenesis, using the Apcmin model of colorectal cancer. Methods: Bmal1 mutant, epithelium-conditional Bmal1 mutant, and photoperiod (day/night cycle) disrupted mice bearing the Apcmin allele were assessed for tumorigenesis. Tumors and normal nontransformed tissue were characterized. Intestinal organoids were assessed for circadian transcription rhythms by RNA sequencing, and in vivo and organoid assays were used to test Bmal1-dependent proliferation and self-renewal. Results: Loss of Bmal1 or circadian photoperiod increases tumor initiation. In the intestinal epithelium the clock regulates transcripts involved in regeneration and intestinal stem cell signaling. Tumors have no self-autonomous clock function and only weak clock function in vivo. Apcmin clock-disrupted tumors show high Yes-associated protein 1 (Hippo signaling) activity but show low Wnt (Wingless and Int-1) activity. Intestinal organoid assays show that loss of Bmal1 increases self-renewal in a Yes-associated protein 1–dependent manner. Conclusions: Bmal1 regulates intestinal stem cell pathways, including Hippo signaling, and the loss of circadian rhythms potentiates tumor initiation. Transcript profiling: GEO accession number: GSE157357.
DOI
10.1016/j.jcmgh.2021.08.001
E-ISSN
2352345X
Recommended Citation
Stokes, Kyle; Nunes, Malika; Trombley, Chantelle; Flôres, Danilo E.F.L.; Wu, Gang; Taleb, Zainab; Alkhateeb, Abedalrhman; Banskota, Suhrid; Harris, Chris; Love, Oliver P.; Khan, Waliul I.; Rueda, Luis; Hogenesch, John B.; and Karpowicz, Phillip. (2021). The Circadian Clock Gene, Bmal1, Regulates Intestinal Stem Cell Signaling and Represses Tumor Initiation. Cellular and Molecular Gastroenterology and Hepatology, 12 (5), 1847-1872.e0.
https://scholar.uwindsor.ca/glierpub/490
PubMed ID
34534703