Abstract

Summary

This study demonstrates that loss of the core circadian clock gene BMAL1 in intestinal epithelial cells increases tumor initiation in a mouse model of colorectal cancer, suggesting the intrinsic gut circadian clock suppresses early tumorigenesis. For lighting designers and healthcare environments, these findings reinforce the importance of maintaining robust circadian entrainment through appropriate light-dark cycles, particularly for shift workers at elevated colorectal cancer risk.
Abstract

Key Findings

  • APCmin/+ mice lacking BMAL1 (full knockout) produced approximately twice the number of intestinal tumors compared to controls.
  • Conditional knockout of BMAL1 specifically in intestinal epithelial cells increased tumor initiation events, but did not affect tumor growth or progression.
  • Prolonged inflammation further increased tumor initiation in both wild-type and conditional knockout animals, but was not implicated in BMAL1-/--induced tumor growth.
  • Clock mutant animals showed a slight decrease in intestinal cell turnover, suggesting disrupted tissue homeostasis as a potential mechanism.
Categories

Categories

The Science of Light: Investigates BMAL1, a core circadian clock gene, and its role in biological timing mechanisms relevant to understanding circadian disruption consequences.
Shift Work & Staff Wellbeing: Contextualizes findings within epidemiological evidence linking shift work and circadian disruption to elevated colorectal cancer risk.
Authors

Author(s)

C Trombley
Publication Date

Publication Year

2020
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