Evidence map›Paper›PMID 39051082›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2024

[Genetic drivers for inflammatory protein markers in colorectal cancer: a Mendelian randomization approach to clinical prognosis study].

H Li, G Li, X Zhang, Y Wang

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2024. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

4 authors.

H LiDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 511340, China.
G LiDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 511340, China.
X ZhangDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 511340, China.
Y WangDepartment of General Surgery, Nanfang Hospital, Southern Medical University, Guangzhou 511340, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the causal relationship between inflammatory protein markers and the risk of colorectal cancer using a Mendelian randomization (MR) approach.

methodsWe obtained data pertaining to colorectal cancer from Genome-Wide Association Study (GWAS) datasets and used 91 inflammatory protein markers as the exposure variables. A two-sample MR analysis model was used to assess the causal link between the inflammatory markers and colorectal cancer risk. The robustness of the results was evaluated through heterogeneity, pleiotropy, and sensitivity analyses using 5 MR models: Inverse Variance Weighted (IVW), Weighted Median, MR Egger, Simple Mode, and Weighted Mode. We examined the mRNA expressions of

resultsUsing the IVW model, MR analysis revealed significant causal associations between a reduced risk of colorectal cancer and lowered expressions of AXIN1 (OR=0.866, 95%

conclusionLowered expressions of inflammatory protein markers AXIN1, β-NGF, and PD-L1 are causally correlated with a reduced risk of colorectal cancer and their expression levels are associated with TNM staging and tumor differentiation. These markers may thus serve as potential targets for colorectal cancer treatment and prevention.

Indexed as

Axin ProteinColorectal NeoplasmsGenome-Wide Association StudyMendelian Randomization AnalysisB7-H1 AntigenBiomarkers, TumorFemaleHumansInflammationMaleMiddle AgedPrognosisRisk FactorsAXIN1 protein, humanAxin ProteinB7-H1 AntigenBiomarkers, TumorCD274 protein, humanclinical studycolorectal cancerinflammatory protein markersMendelian randomization

Identifiers

PMID39051082
PMCPMC11270664

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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 Socratic graph.