Evidence map›Paper›PMID 39205564›Full record

ArticleAsian Pacific journal of cancer prevention : APJCP2024

Clinical Significance of TNFSF14/LIGHT and CD160 in Gastric Cancer and Peptic Ulcer Dyspepsia.

Mohsen Keykhosravi, Hossein Asgarian-Omran, Reza Valadan, Mohsen Tehrani, Seyed Mohammad Javadzadeh, Saeid Taghiloo, Ahmad Najafi, Qasem Fatehi, Islam Majd, Abolghasem Ajami

Abstract read
In one paragraph

Article in Asian Pacific journal of cancer prevention : APJCP, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

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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

2 citing papers in PubMed.

  1. Genetic variants ofFrontiers in immunology · 2026
    Article
  2. PPIFJournal of translational medicine · 2025
    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

10 authors.

Mohsen KeykhosraviDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.ORCID 0000-0002-2429-1418
Hossein Asgarian-OmranDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Reza ValadanDepartment of Immunology, Molecular and Cell Biology Research Center, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Mohsen TehraniDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Seyed Mohammad JavadzadehDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Saeid TaghilooDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Ahmad NajafiDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Qasem FatehiBabol University of Medical Science, Mazandaran, Babol, Iran.
Islam MajdArdebil University of Medical science, Ardebil, Iran.
Abolghasem AjamiDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrevious studies have reported the role of the Herpes Virus Entry Mediator (HVEM) in various cancer including gastric cancer. However, the expression level and clinical significance of CD160 and Tumor Necrosis Factor Ligand Superfamily Member 14 (TNFSF14) pathways in gastric cancer and gastric dyspepsia patients have remained unexplored.

methodsThe study involved the collection of gastric tissue biopsies from 42 patients with non-ulcerative dyspepsia (NUD) as the control group, 43 gastric cancer (GC) patients, and 48 patients with peptic-ulcerative dyspepsia (PUD). All the patients were endoscopically examined at Imam Khomeini Hospital in Sari, Mazandaran, Iran. The expression levels of TNFSF14 and CD160 mRNA were assessed using quantitative real-time PCR (qPCR) with the SYBR Green method. Statistical analysis was performed to investigate the potential association between the clinical and experimental data.

resultsAmong the 133 gastric endoscopic biopsies examined, LIGHT exhibited a significant overexpression in GC patients (p-value < 0.01). Moreover, the expression of TNFSF14 was higher in GC patients with stages I and II (p-value<0.05). Furthermore, GC patients with TNM stages III+IV were accompanied by high expression levels of LIGHT (p-value < 0.01) as well as CD160 (p-value<0.05). The expression of CD160 was also higher in younger adults with PUD (p-value<0.05). Whereas TNFSF14 exhibited higher expression in older adults with GC (p-value<0.05). Furthermore, this research provided insights into the potential biological pathways and significant gene enrichment of TNFSF14 and CD160, suggesting the potential role of CD160 and TNFSF14 in the regulation of immune system in GC and PUD.

conclusionThese findings suggest the possible role of LIGHT and CD160 expression in gastric cancer patients in immune dysregulation toward gastric cancer. Targeted immunotherapy that harnessing co-stimulatory molecules like LIGHT and CD160 could be a promising approach in the treatment of GC as well as potential GC tumor markers.

Indexed as

Antigens, CDDyspepsiaGPI-Linked ProteinsPeptic UlcerStomach NeoplasmsTumor Necrosis Factor Ligand Superfamily Member 14AdultAgedBiomarkers, TumorCase-Control StudiesClinical RelevanceFemaleFollow-Up StudiesHumansMaleMiddle AgedAntigens, CDBiomarkers, TumorCD160 protein, humanGPI-Linked ProteinsReceptors, ImmunologicRNA, MessengerTNFSF14 protein, humanTumor Necrosis Factor Ligand Superfamily Member 14CD160 antigenDyspepsiaGastric cancerTumor Necrosis Factor Ligand Superfamily Member 14

Identifiers

PMID39205564
PMCPMC11495460

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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.