Evidence map›Paper›PMID 32337262›Full record

ArticleBioMed research international2020

Construction of a CXC Chemokine-Based Prediction Model for the Prognosis of Colon Cancer.

Kaisheng Liu, Minshan Lai, Shaoxiang Wang, Kai Zheng, Shouxia Xie, Xiao Wang

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.3field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. The Significance of CXCL1 in Cancer: An Overview of Molecular Mechanisms.International journal of molecular sciences · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Kaisheng Liu *The First Affiliated Hospital of Southern University of Science and Technology, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen, Guangdong, China.
Minshan Lai *School of Pharmaceutical Sciences, Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Shaoxiang WangSchool of Pharmaceutical Sciences, Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Kai ZhengSchool of Pharmaceutical Sciences, Shenzhen University Health Science Center, Shenzhen, Guangdong, China.
Shouxia XieThe First Affiliated Hospital of Southern University of Science and Technology, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0002-3327-6332
Xiao WangThe First Affiliated Hospital of Southern University of Science and Technology, The Second Clinical Medical College of Jinan University, Shenzhen People's Hospital, Shenzhen, Guangdong, China.ORCID https://orcid.org/0000-0001-8824-6280
Jinan University · CNShenzhen University Health Science Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colon cancer is the third most common cancer, with a high incidence and mortality. Construction of a specific and sensitive prediction model for prognosis is urgently needed. In this study, profiles of patients with colon cancer with clinical and gene expression data were downloaded from Gene Expression Omnibus and The Cancer Genome Atlas (TCGA). CXC chemokines in patients with colon cancer were investigated by differential expression gene analysis, overall survival analysis, receiver operating characteristic analysis, gene set enrichment analysis (GSEA), and weighted gene coexpression network analysis. CXCL1, CXCL2, CXCL3, and CXCL11 were upregulated in patients with colon cancer and significantly correlated with prognosis. The area under curve (AUC) of the multigene forecast model of CXCL1, CXCL11, CXCL2, and CXCL3 was 0.705 in the GSE41258 dataset and 0.624 in TCGA. The prediction model was constructed using the risk score of the multigene model and three clinicopathological risk factors and exhibited 92.6% and 91.8% accuracy in predicting 3-year and 5-year overall survival of patients with colon cancer, respectively. In addition, by GSEA, expression of CXCL1, CXCL11, CXCL2, and CXCL3 was correlated with several signaling pathways, including NOD-like receptor, oxidative phosphorylation, mTORC1, interferon-gamma response, and IL6/JAK/STAT3 pathways. Patients with colon cancer will benefit from this prediction model for prognosis, and this will pave the way to improve the survival rate and optimize treatment for colon cancer.

Indexed as

Chemokine CXCL1Chemokine CXCL11Chemokine CXCL2Chemokines, CXCColonic NeoplasmsFemaleGene Expression Regulation, NeoplasticGene Regulatory NetworksHumansInterferon-gammaInterleukin-6MaleMechanistic Target of Rapamycin Complex 1Middle AgedMultivariate AnalysisNLR ProteinsChemokine CXCL1Chemokine CXCL11Chemokine CXCL2Chemokines, CXCCXCL11 protein, humanCXCL1 protein, humanCXCL2 protein, humanCXCL3 protein, humanInterferon-gammaInterleukin-6Mechanistic Target of Rapamycin Complex 1NLR Proteins

Identifiers

PMID32337262
PMCPMC7150705
OpenAlexW3015100666

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Registered trials

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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.