Evidence map›Paper›PMID 36389694›Full record

ArticleFrontiers in immunology2022

A novel oxidative stress- and ferroptosis-related gene prognostic signature for distinguishing cold and hot tumors in colorectal cancer.

Xu Wang, Yuanmin Xu, Longfei Dai, Zhen Yu, Ming Wang, Shixin Chan, Rui Sun, Qijun Han, Jiajie Chen, Xiaomin Zuo and 7 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 2 pooled it
5.6field-weighted citation impact, top 3% 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

24 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

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  13. Ferroptosis: the balance between death and survival in colorectal cancer.International journal of biological sciences · 2024
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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

17 authors at 3 institutions in 1 country.

Xu WangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yuanmin XuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Longfei DaiDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Zhen YuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Ming WangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Shixin ChanDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Rui SunDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Qijun HanDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Jiajie ChenDepartment of Dermatology, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Xiaomin ZuoDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Zhenglin WangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Xianyu HuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yang YangDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Hu ZhaoDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Kongwang HuDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Huabing ZhangDepartment of Biochemistry and Molecular Biology, Metabolic Disease Research Center, School of Basic Medicine, Anhui Medical University, Hefei, Anhui, China.
Wei ChenDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
First Affiliated Hospital of Anhui Medical University · CNAnhui Medical University · CNChuzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress and ferroptosis exhibit crosstalk in many types of human diseases, including malignant tumors. We aimed to develop an oxidative stress- and ferroptosis-related gene (OFRG) prognostic signature to predict the prognosis and therapeutic response in patients with colorectal cancer (CRC). Thirty-four insertion genes between oxidative stress-related genes and ferroptosis-related genes were identified as OFRGs. We then performed bioinformatics analysis of the expression profiles of 34 OFRGs and clinical information of patients obtained from multiple datasets. Patients with CRC were divided into three OFRG clusters, and differentially expressed genes (DEGs) between clusters were identified. OFRG clusters correlated with patient survival and immune cell infiltration. Prognosis-related DEGs in three clusters were used to calculate the risk score, and a prognostic signature was constructed according to the risk score. In this study, patients in the low-risk group had better prognosis, higher immune cell infiltration levels, and better responses to fluorouracil-based chemotherapy and immune checkpoint blockade therapy than high-risk patients; these results were successfully validated with multiple independent datasets. Thus, low-risk CRC could be defined as hot tumors and high-risk CRC could be defined as cold tumors. To further identify potential biomarkers for CRC, the expression levels of five signature genes in CRC and adjacent normal tissues were further verified

Indexed as

Colorectal NeoplasmsFerroptosisBiomarkers, TumorGene Expression Regulation, NeoplasticHumansOxidative StressPrognosisBiomarkers, Tumorchemotherapycolorectal cancerferroptosisimmunotherapyoxidative stressprognosistumor microenvironment

Identifiers

PMID36389694
PMCPMC9660228
OpenAlexW4307871565

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.