Evidence map›Paper›PMID 40783879›Full record

ArticleDiscover oncology2025

Genetically predicted inflammatory protein mediate the association between lipidome and colon cancer.

Sun Jiawei, Jiang Yixin, Shen Ting, Guan Yining

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Sun JiaweiShulan International Medical College, Zhejiang Shuren University, Hangzhou, 310052, China. itsjunenow@zju.edu.cn.
Jiang YixinShulan International Medical College, Zhejiang Shuren University, Hangzhou, 310052, China.
Shen TingShulan International Medical College, Zhejiang Shuren University, Hangzhou, 310052, China.
Guan YiningShulan International Medical College, Zhejiang Shuren University, Hangzhou, 310052, China.

Funding

Natural Science Foundation of Zhejiang Province LQ23H030001
6 · The paper itself

Abstract

backgroundPrevious studies show correlations between colon cancer, dyslipidemia, and inflammatory proteins. However, the exact causal relationships are still unclear and no comprehensive analysis exists.

methodsWe used a two-sample Mendelian Randomization (MR) strategy to assess the link between lipidomes and colon cancer risk. Bayesian Weighted Mendelian Randomization (BWMR) and MR-robust adjusted profile score (MR-RAPS) were employed to validate our findings. Furthermore, inverse MR analysis was conducted to investigate the possibility of reverse causation. Through a comprehensive two-step MR analysis, we identified the mediating effect of inflammatory factors. Various sensitivity analyses were carried out to ensure the reliability and robustness of our results.

resultsOur MR analysis highlighted negative correlations between Phosphatidylcholine (O-16:1_18:0) (OR, 95% CI 0.771, (0.610, 0.975)), Phosphatidylethanolamine (O-16:1_22:5) (OR, 95% CI 0.788, (0.664, 0.934)), Phosphatidylethanolamine (O-18:1_18:2) (OR, 95% CI 0.825, (0.708, 0.960)) and colon cancer. In contrast, we found positive correlations with Sterol ester (27:1/18:3) (OR, 95% CI 1.278, (1.068, 1.530)), Phosphatidylcholine (18:0_22:5) (OR, 95% CI 1.322, (1.118, 1.563)), Triacylglycerol (46:1) (OR, 95% CI 1.272, (1.047, 1.546)), Triacylglycerol (46:2) (OR, 95% CI 1.236, (1.034, 1.478)) and colon cancer. Furthermore, mediation analysis revealed that a fraction of the impacts of Phosphatidylcholine (18:0_22:5) and Phosphatidylethanolamine (O-16:1_22:5) on colon cancer were mediated by TNF-related apoptosis-inducing ligand levels.

conclusionThis study presents evidence supporting potential causal correlations between 7 lipidome levels and colon cancer, based on Mendelian randomization analyses. Additionally, inflammatory factors mediate some of these effects.

Indexed as

Causal relationshipColon cancerInflammatory proteinLipidomeMendelian randomizationSingle nucleotide polymorphism

Identifiers

PMID40783879
PMCPMC12336103

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.