Back to Search Start Over

β-Hydroxybutyrate suppresses colorectal cancer.

Authors :
Dmitrieva-Posocco O
Wong AC
Lundgren P
Golos AM
Descamps HC
Dohnalová L
Cramer Z
Tian Y
Yueh B
Eskiocak O
Egervari G
Lan Y
Liu J
Fan J
Kim J
Madhu B
Schneider KM
Khoziainova S
Andreeva N
Wang Q
Li N
Furth EE
Bailis W
Kelsen JR
Hamilton KE
Kaestner KH
Berger SL
Epstein JA
Jain R
Li M
Beyaz S
Lengner CJ
Katona BW
Grivennikov SI
Thaiss CA
Levy M
Source :
Nature [Nature] 2022 May; Vol. 605 (7908), pp. 160-165. Date of Electronic Publication: 2022 Apr 27.
Publication Year :
2022

Abstract

Colorectal cancer (CRC) is among the most frequent forms of cancer, and new strategies for its prevention and therapy are urgently needed <superscript>1</superscript> . Here we identify a metabolite signalling pathway that provides actionable insights towards this goal. We perform a dietary screen in autochthonous animal models of CRC and find that ketogenic diets exhibit a strong tumour-inhibitory effect. These properties of ketogenic diets are recapitulated by the ketone body β-hydroxybutyrate (BHB), which reduces the proliferation of colonic crypt cells and potently suppresses intestinal tumour growth. We find that BHB acts through the surface receptor Hcar2 and induces the transcriptional regulator Hopx, thereby altering gene expression and inhibiting cell proliferation. Cancer organoid assays and single-cell RNA sequencing of biopsies from patients with CRC provide evidence that elevated BHB levels and active HOPX are associated with reduced intestinal epithelial proliferation in humans. This study thus identifies a BHB-triggered pathway regulating intestinal tumorigenesis and indicates that oral or systemic interventions with a single metabolite may complement current prevention and treatment strategies for CRC.<br /> (© 2022. The Author(s), under exclusive licence to Springer Nature Limited.)

Details

Language :
English
ISSN :
1476-4687
Volume :
605
Issue :
7908
Database :
MEDLINE
Journal :
Nature
Publication Type :
Academic Journal
Accession number :
35477756
Full Text :
https://doi.org/10.1038/s41586-022-04649-6