PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
April 5, 2026Cancer Research0 citations

Abstract 6156: Omega-6 lipid-gene module linked to colorectal cancer pre-metastatic niche

View Full Paper
RSRamani SoundararajanLPLance PfliegerGUGunjan Upadhyay

Key Points

  • The aim is to explore the connection between omega-6 fatty acids and inflammatory gene expression in colorectal cancer.
  • Conducted multi-omics analysis of arachidonic acid-derived lipid mediators and transcriptomes from human colorectal cancer samples.
  • Analyzed gene expression in syngeneic mouse models fed omega-6:omega-3 diets.
  • Correlated macrophage gene expression signatures with identified lipid-gene modules.
  • Identified a pro-inflammatory lipid-gene module significantly associated with metastasis in human tumors.
  • Observed significant enrichment of coagulation and EMT-related genes in murine tumors fed an omega-6 diet.
  • Noted a decrease in Serpina1 protein expression in the liver, indicating localized inflammation associated with metastasis.

Abstract

Abstract Introduction: We recently reported (Soundararajan et. al., GUT, 2024) a strong pro-inflammatory lipid mediator bias in colorectal cancer (CRC), possibly related to the omega-6 rich fatty acid preponderance in western-style diets. The current project expands on those findings, linking omega-6 fatty acids to expression of inflammatory genes in human CRC and mouse models. Method: We performed an integrative, multi-omics, weighted gene co-expression network analysis (WGCNA) of 25 quantified arachidonic acid-derived lipid mediators with whole transcriptomes from 293 primary and 77 metastatic human CRCs, to identify a lipid-gene module significantly associated with metastasis. In mice fed omega-6:omega-3 (10:1 w/w) vs. control (1:1 w/w) diets, we analyzed syngeneic CRC subcutaneous tumors using whole transcriptome RNA-sequencing. THP1-derived gene expression signatures for M0, M1 and M2 macrophages were correlated with the lipid-gene module. Results: In the human tumors using an unsupervised analysis, we identified a pro-inflammatory lipid-gene module, linked to the clinical feature of metastasis (P 1.1e-42), with prominence of “hallmark” genes linked to coagulation, complement, inflammation and EMT/tumor progression and associated with M1 macrophages. Analysis of murine tumors derived from animals fed a diet enriched with omega-6 fatty acids revealed a significant (p 3.7329E-06), shared enrichment of 18 coagulation and EMT related genes --orthologous to those identified in the pro-inflammatory human lipid-gene module. Among the 18 genes, SerpinA1b, SerpinA1d, SerpinA3k, Ambp and Plg with anti-inflammatory and coagulation- inhibitory properties were downregulated in omega-6 fed mice. Moreover, we observed a dramatic decrease in Serpina1 protein expression in the hepatic sinusoids in omega-6 mice. Conclusion: A human tumor pro-inflammatory lipid-gene module was identified, and its gene expression was shared with tumors derived from mice fed with an omega-6-rich diet. Hallmark gene analysis found inflammation and deranged coagulation prominent. In omega-6 fed mice, decrease in Serpina1 protein expression in liver sinusoidal endothelial cells---the first target of metastasizing cells---suggests localized inflammation with enhanced coagulation. Collectively, these data suggest omega-6 enriched murine and human western diets may foster the development of an inflammatory, coagulopathic pre-metastatic liver niche, with M1 macrophages as the main contributors of CRC inflammation. Citation Format: Ramani Soundararajan, Lance Pflieger, Gunjan Upadhyay, Michelle M. Maurin, Mingli Yang, Michael Schell, McKayla Carr, Ahalya Sekhar, Rachel Kenis, Heiman Wang, Michael Nebozhyn, Andrey Loboda, Aejaz Nasir, W Jack Pledger, Ganesh V. Halade, Timothy J. Yeatman. Omega-6 lipid-gene module linked to colorectal cancer pre-metastatic niche abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 6156.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Soundararajan et al. (2026) studied this question.

synapsesocial.com/papers/69d1fdf7a79560c99a0a4608https://doi.org/10.1158/1538-7445.am2026-6156
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Abstract 5046: Integrating omics data unravels potential mechanisms linking diet-related inflammation and colorectal cancer risk2026
  2. 2Integrative multi-omics identification and functional validation of potential targets linking metabolism–immune–colorectal cancer causal pathway2025 · 3 citations
  3. 3Abstract 6126: Multiomics integration unveils a shifted balance in the sphingosine-1 phosphate/ceramide rheostat fueled by macrophage immunosuppression in metastatic colorectal cancer2026
  4. 4Abstract 2316: Circulating lipid and bile acid metabolites as predictors of colorectal cancer risk: A multi-cohort metabolomics meta-analysis2026
  5. 5Macrophage-derived IL-6 reprograms lipid metabolism to promote colorectal cancer development through USP14-mediated FASN deubiquitination2026