Evidence map›Paper›PMID 38166604›Full record

ArticleBMC genomics2024

Prognostic value of oxidative stress-related genes in colorectal cancer and its correlation with tumor immunity.

Leilei Yang, Chengfeng Fang, Ruili Zhang, Shenkang Zhou

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 9 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Leilei Yang *Department of Gastrointestinal Surgery, Key Laboratory of Minimally Invasive Techniques & Rapid Rehabilitation of Digestive System Tumor of Zhejiang Province (Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University), No. 150, Ximen Street, Linhai, Taizhou, 317000, Zhejiang, China.
Chengfeng Fang *Department of Gastrointestinal Surgery, Key Laboratory of Minimally Invasive Techniques & Rapid Rehabilitation of Digestive System Tumor of Zhejiang Province (Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University), No. 150, Ximen Street, Linhai, Taizhou, 317000, Zhejiang, China.
Ruili ZhangDepartment of Gastrointestinal Surgery, Key Laboratory of Minimally Invasive Techniques & Rapid Rehabilitation of Digestive System Tumor of Zhejiang Province (Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University), No. 150, Ximen Street, Linhai, Taizhou, 317000, Zhejiang, China. zhangrl@enzemed.com.
Shenkang ZhouDepartment of Gastrointestinal Surgery, Key Laboratory of Minimally Invasive Techniques & Rapid Rehabilitation of Digestive System Tumor of Zhejiang Province (Taizhou Hospital of Zhejiang Province affiliated to Wenzhou Medical University), No. 150, Ximen Street, Linhai, Taizhou, 317000, Zhejiang, China. 13736249308@163.com.
Wenzhou Medical University · CN

Funding

Taizhou Science and Technology Department Project 21ywa08, 22ywa13Zhejiang Medical and Health Science and Technology Plan Project 2022PY028
6 · The paper itself

Abstract

Oxidative stress (OS) plays an essential role in chronic diseases such as colorectal cancer (CRC). In this study, we aimed to explore the relation between oxidative stress-related genes and CRC prognosis and their involvement in the immune microenvironment. Totally 101 OS-related genes were selected from the MsigDB database. Then, univariate Cox regression was used to explore the prognostic value of the selected genes correlated with the CRC patient survival in the TCGA database. A total of 9 prognostic OS-related genes in CRC were identified. Based on consensus clustering, CRC patients were then categorized into two molecular subtypes. A prognostic risk model containing 8 genes was established using Lasso regression, and CRC patients were divided into high or low-risk groups based on the median risk scores. The predictive value of the 8 genes in CRC prognosis was validated using ROC curves, which indicate that CTNNB1, STK25, RNF112, SFPQ, MMP3, and NOL3 were promising prognostic biomarkers in CRC. Furthermore, the immune cell infiltration levels in different risk groups or CRC subtypes were analyzed. We found that the high-risk or C1 subtype had immunosuppressive microenvironment, which might explain the unfavorable prognosis in the two groups of CRC patients. Additionally, functional experiments were conducted to investigate the effects of OS-related genes on CRC cell proliferation, stemness, and apoptosis. We found that CTNNB1, HSPB1, MMP3, and NOL3 were upregulated in CRC tissues and cells. Knockdown of CTNNB1, HSPB1, MMP3, and NOL3 significantly suppressed CRC cell proliferation, stemness and facilitated CRC cell apoptosis. In conclusion, we established prognostic CRC subtypes and an eight-gene risk model, which may provide novel prognostic indicators and benefit the design of individualized therapeutic strategies for CRC patients.

Indexed as

Colorectal NeoplasmsMatrix Metalloproteinase 3ApoptosisCell ProliferationHippo KinasesHumansIntracellular Signaling Peptides and ProteinsPrognosisProtein Serine-Threonine KinasesTumor MicroenvironmentHippo KinasesIntracellular Signaling Peptides and ProteinsMatrix Metalloproteinase 3Protein Serine-Threonine KinasesSTK25 protein, humanBiomarkerColorectal cancerOxidative stressPrognosisRisk model

Identifiers

PMID38166604
PMCPMC10759670
OpenAlexW4390495511

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.