High-fat diet driven post-operative colon cancer recurrence is dependent upon genetic susceptibility to deoxycholic acid

Cancer Lett. 2025 Oct 28:631:217943. doi: 10.1016/j.canlet.2025.217943. Epub 2025 Jul 22.

Abstract

The development of postoperative recurrent tumors or metastasis following surgical resection of colorectal cancer remains a major obstacle to colon cancer cure. While a high-fat diet is a risk factor for the development of recurrence, studies that examine the molecular mechanism by which diet drives postoperative tumors have been lacking. Here, using a murine model that mimics postoperative tumor formation, we show that the tumorigenic influence of a high-fat diet strongly depends on the genetic backbone of the primary tumor cells. We identify deoxycholic acid as a major contributor to the promotion of tumor recurrence only when the primary cancer cell has an APC-driving mutation. We investigate the deoxycholic acid effect on the proliferation of organoids and identify the organoid response to deoxycholic acid treatment, including the transcriptome expression and transfer RNA abundance, modification, and charging. The integrated analysis of mRNA and tRNA sequencing results reveals enhanced decoding of codons in proliferation-promoting genes. Our results provide a new understanding of how both diet and tumor genetics together lead to postoperative colorectal cancer recurrence.

Keywords: Bile acid; Cancer genetics; Colorectal cancer; High-fat diet; Protein synthesis; Recurrence.

MeSH terms

  • Animals
  • Cell Proliferation / drug effects
  • Colonic Neoplasms* / genetics
  • Colonic Neoplasms* / pathology
  • Colonic Neoplasms* / surgery
  • Deoxycholic Acid* / adverse effects
  • Deoxycholic Acid* / toxicity
  • Diet, High-Fat* / adverse effects
  • Disease Models, Animal
  • Gene Expression Regulation, Neoplastic / drug effects
  • Genetic Predisposition to Disease*
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Neoplasm Recurrence, Local* / chemically induced
  • Neoplasm Recurrence, Local* / genetics
  • Neoplasm Recurrence, Local* / pathology

Substances

  • Deoxycholic Acid