Genetic and microenvironmental evolution of colorectal liver metastases under chemotherapy

Cell Rep Med. 2024 Dec 17;5(12):101838. doi: 10.1016/j.xcrm.2024.101838. Epub 2024 Dec 3.

Abstract

Drug resistance limits the efficacy of chemotherapy for colorectal cancer liver metastasis (CRLM). However, the evolution of CRLM during drug treatment remains poorly elucidated. Multi-omics and treatment response data from 115 samples of 49 patients with CRLM undergoing bevacizumab (BVZ)-based chemotherapy show little difference in genomic alterations in 92% of cases, while remarkable differences are observed at the transcriptomic level. By decoupling intrinsic and acquired resistance, we find that hepatocyte and myeloid cell infiltration contribute to 38.5% and 23.1% of acquired resistance, respectively. Importantly, SMAD4 mutations and chr20q copy-number gain are associated with intrinsic chemoresistance. Gene interference experiments suggest that SMAD4R361H/C mutations confer BVZ and 5-fluorouracil (5-FU) resistance through STAT3 signaling. Notably, supplementing BVZ and 5-FU with the STAT3 inhibitor GB201 restores therapeutic efficacy in SMAD4R361H/C cancer cells. Our study uncovers the evolutionary dynamics of CRLM and its microenvironment during treatment and offers strategies to overcome drug resistance.

Keywords: Bevacizumab; SMAD4 mutation; cancer genomics; chemoresistance; chr20q copy-number gain; colorectal liver metastases; tumor microenvironment.

MeSH terms

  • Animals
  • Bevacizumab* / pharmacology
  • Bevacizumab* / therapeutic use
  • Cell Line, Tumor
  • Colorectal Neoplasms* / drug therapy
  • Colorectal Neoplasms* / genetics
  • Colorectal Neoplasms* / pathology
  • Drug Resistance, Neoplasm* / genetics
  • Female
  • Fluorouracil* / pharmacology
  • Fluorouracil* / therapeutic use
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Liver Neoplasms* / drug therapy
  • Liver Neoplasms* / genetics
  • Liver Neoplasms* / secondary
  • Male
  • Mutation* / genetics
  • STAT3 Transcription Factor* / genetics
  • STAT3 Transcription Factor* / metabolism
  • Signal Transduction / drug effects
  • Smad4 Protein* / genetics
  • Smad4 Protein* / metabolism
  • Tumor Microenvironment* / drug effects
  • Tumor Microenvironment* / genetics

Substances

  • Bevacizumab
  • STAT3 Transcription Factor
  • Fluorouracil
  • Smad4 Protein
  • SMAD4 protein, human
  • STAT3 protein, human