The cholesterol biosynthesis enzyme FAXDC2 couples Wnt/β-catenin to RTK/MAPK signaling

• Published in: The Journal of clinical investigation 2024-03, Vol.134 (6), p.1-18
• Main Authors: Madan, Babita, Wadia, Shawn R, Patnaik, Siddhi, Harmston, Nathan, Tan, Emile, Tan, Iain Bee Huat, Nes, W David, Petretto, Enrico, Virshup, David M
• Format: Article
• Language: English
• Subjects: Biosynthesis; Cholesterol; Dehydrogenases; Demethylation; Enzymes; Fatty acids; Genes; Homeostasis; Kinases; Ligands; MAP kinase; Mutation; Pancreatic cancer; Phosphorylation; Senescence; Signal transduction; Stem cells; Sterols; Tumors; Wnt protein; β-Catenin
• ISSN: 0021-9738; 1558-8238
• DOI: 10.1172/JCI171222.

Writs, cholesterol, and MAPK signaling are essential for development and adult homeostasis. Here, we report that fatty acid hydroxylase domain containing 2 (FAXDC2), a previously uncharacterized enzyme, functions as a methyl sterol oxidase catalyzing C4 demethylation in the Kandutsch-Russell branch of the cholesterol biosynthesis pathway. FAXDC2, a paralog of MSM01, regulated the abundance of the specific C4-methyl sterols lophenol and dihydro-T-MAS. Highlighting its clinical relevance, FAXDC2 was repressed in Wnt/ß-catenin-high cancer xenografts, in a mouse genetic model of Wnt activation, and in human colorectal cancers. Moreover, in primary human colorectal cancers, the sterol lophenol, regulated by FAXDC2, accumulated in the cancerous tissues and not in adjacent normal tissues. FAXDC2 linked Wnts to RTK/MAPK signaling. Wnt inhibition drove increased recycling of RTKs and activation of the МАРК pathway, and this required FAXDC2. Blocking Wnt signaling in Wnt-high cancers caused both differentiation and senescence; and this was prevented by knockout of FAXDC2. Our data show the integration of 3 ancient pathways, Wnts, cholesterol synthesis, and RTK/MAPK signaling, in cellular proliferation and differentiation.