Evidence map›Paper›PMID 37404760›Full record

ArticleFrontiers in oncology2023

Identification of a six-gene signature to predict survival and immunotherapy effectiveness of gastric cancer.

Qi Wang, Biyuan Zhang, Haiji Wang, Mingming Hu, Hui Feng, Wen Gao, Haijun Lu, Ye Tan, Yinying Dong, Mingjin Xu and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
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

12 authors at 2 institutions in 1 country.

Qi WangDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Biyuan ZhangDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Haiji WangDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Mingming HuDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Hui FengDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Wen GaoDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Haijun LuDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Ye TanDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Yinying DongDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Mingjin XuDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Tianhui GuoDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Xiaomeng JiDepartment of Radiation Oncology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong, China.
Qingdao University · CNAffiliated Hospital of Qingdao University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gastric cancer (GC) ranks as the fifth most prevalent malignancy and the second leading cause of oncologic mortality globally. Despite staging guidelines and standard treatment protocols, significant heterogeneity exists in patient survival and response to therapy for GC. Thus, an increasing number of research have examined prognostic models recently for screening high-risk GC patients. Methods: We studied DEGs between GC tissues and adjacent non-tumor tissues in GEO and TCGA datasets. Then the candidate DEGs were further screened in TCGA cohort through univariate Cox regression analyses. Following this, LASSO regression was utilized to generate prognostic model of DEGs. We used the ROC curve, Kaplan-Meier curve, and risk score plot to evaluate the signature's performance and prognostic power. ESTIMATE, xCell, and TIDE algorithm were used to explore the relationship between the risk score and immune landscape relationship. As a final step, nomogram was developed in this study, utilizing both clinical characteristics and a prognostic model. Results: There were 3211 DEGs in TCGA, 2371 DEGs in GSE54129, 627 DEGs in GSE66229, and 329 DEGs in GSE64951 selected as candidate genes and intersected with to obtain DEGs. In total, the 208 DEGs were further screened in TCGA cohort through univariate Cox regression analyses. Following this, LASSO regression was utilized to generate prognostic model of 6 DEGs. External validation showed favorable predictive efficacy. We studied interaction between risk models, immunoscores, and immune cell infiltrate based on six-gene signature. The high-risk group exhibited significantly elevated ESTIMATE score, immunescore, and stromal score relative to low-risk group. The proportions of CD4 Conclusion: In conclusion, we discovered a 6 gene signature to forecast GC patients' OS. This risk signature proves to be a valuable clinical predictive tool for guiding clinical practice.

Indexed as

bioinformaticsgastric carcinomamicroenvironmentnomogramprognostic model

Identifiers

PMID37404760
PMCPMC10316024
OpenAlexW4381251826

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.