Evidence map›Paper›PMID 35173464›Full record

ArticleInternational journal of general medicine2022

SEMA3D Plays a Critical Role in Peptic Ulcer Disease-Related Carcinogenesis Induced by

Zhiyu Wang, Yaning Wei, Lin An, Kunjie Wang, Dan Hong, Yan Shi, Aimin Zang, Shenyong Su, Wenwen Li

Open access · goldAbstract read
In one paragraph

Article in International journal of general medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 54% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

9 authors at 1 institution in 1 country.

Zhiyu WangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Yaning WeiDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Lin AnDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Kunjie WangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Dan HongDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Yan ShiDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Aimin ZangDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Shenyong SuDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Wenwen LiDepartment of Medical Oncology, Affiliated Hospital of Hebei University, Baoding, Hebei Province, People's Republic of China.
Affiliated Hospital of Hebei University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune cell infiltration plays a critical role in regulating peptic ulcer disease (PUD) and gastrointestinal cancer (GC). However, regulators of the cell signaling hubs remain unclear.

aimThis study characterizes genes that are differentially expressed in PUD and GC tissue samples. Bioinformatics is used to define the immune-associated hub genes associated with the malignant transfer process of PUD to GC.

methodsTotal expression data from PUD and early-stage GC tissue samples were obtained from GEO and TCGA. Differentially expressed genes were assessed and immunological enrichment analysis was performed. Protein-protein interaction (PPI) and Cytoscape analysis were used together to identify the hub genes. CIBERSORT and COX analysis were used to analyze the differentially infiltrated immune cell landscapes and determine HR scores of the hub genes.

resultsExpression data identified 437 DEGs as common to both GC and PUD tissue. Of these, 49 immune-related DEGs were grouped by function, and seven hub genes were identified by PPI analysis. The NRP2 and SEMA3D genes were then selected for survival analysis. SEMA3D had a higher hazard ratio than NRP2 and was defined as the hub for PUD carcinogenesis.

conclusionSEMA3D was characterized as the hub gene for PUD carcinogenesis.

Indexed as

gastric cancerH. pyloriimmunological micro-environmentpeptic ulcer diseaseSEMA3D

Identifiers

PMID35173464
PMCPMC8841493
OpenAlexW4210878438

What OpenQuestion holds

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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.