Evidence map›Paper›PMID 38357542›Full record

ArticleFrontiers in immunology2024

Unraveling the potential of CD8, CD68, and VISTA as diagnostic and prognostic markers in patients with pancreatic ductal adenocarcinoma.

Fereshteh Rezagholizadeh, Fatemeh Tajik, Morteza Talebi, Seyed Reza Taha, Mahdieh Shariat Zadeh, Pooya Farhangnia, Hamideh Sadat Hosseini, Aram Nazari, Shabnam Mollazadeh Ghomi, Seyede Mahtab Kamrani Mousavi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 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
2.8field-weighted citation impact, top 8% 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, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Exploring the Therapeutic Potential ofCurrent pharmaceutical design · 2025
    Article
  5. Review
  6. Article
  7. VISTA-mediated immune evasion in cancer.Experimental & molecular medicine · 2024
    Review
  8. Article
  9. Review
  10. Article
  11. 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

14 authors at 1 institution in 1 country.

Fereshteh RezagholizadehCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Fatemeh TajikOncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Morteza TalebiCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Seyed Reza Taha *Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Mahdieh Shariat Zadeh *Oncopathology Research Center, Iran University of Medical Sciences, Tehran, Iran.
Pooya Farhangnia *Department of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Hamideh Sadat HosseiniCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Aram NazariCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Shabnam Mollazadeh GhomiCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Seyede Mahtab Kamrani MousaviCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Niloofar Haeri MoghaddamCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Hossein KhorramdelazadDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mohammad Taghi JoghataeiCellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran.
Elahe SafariDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Iran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Pancreatic cancer is a truculent disease with limited treatment options and a grim prognosis. Immunotherapy has shown promise in treating various types of cancer, but its effectiveness in pancreatic cancer has been lacking. As a result, it is crucial to identify markers associated with immunological pathways in order to improve the treatment outcomes for this deadly cancer. The purpose of this study was to investigate the diagnostic and prognostic significance of three markers, CD8, CD68, and VISTA, in pancreatic ductal adenocarcinoma (PDAC), the most common subtype of pancreatic cancer. Methods: We analyzed gene expression data from Gene Expression Omnibus (GEO) database using bioinformatics tools. We also utilized the STRING online tool and Funrich software to study the protein-protein interactions and transcription factors associated with CD8, CD68, and VISTA. In addition, tissue microarray (TMA) and immunohistochemistry (IHC) staining were performed on 228 samples of PDAC tissue and 10 samples of normal pancreatic tissue to assess the expression levels of the markers. We then correlated these expression levels with the clinicopathological characteristics of the patients and evaluated their survival rates. Results: The analysis of the GEO data revealed slightly elevated levels of VISTA in PDAC samples compared to normal tissues. However, there was a significant increase in CD68 expression and a notable reduction in CD8A expression in pancreatic cancer. Further investigation identified potential protein-protein interactions and transcription factors associated with these markers. The IHC staining of PDAC tissue samples showed an increased expression of VISTA, CD68, and CD8A in pancreatic cancer tissues. Moreover, we found correlations between the expression levels of these markers and certain clinicopathological features of the patients. Additionally, the survival analysis revealed that high expression of CD8 was associated with better disease-specific survival and progression-free survival in PDAC patients. Conclusion: These findings highlight the potential of CD8, CD68, and VISTA as diagnostic and prognostic indicators in PDAC.

Indexed as

Carcinoma, Pancreatic DuctalPancreatic NeoplasmsB7 AntigensCD68 MoleculeCD8 AntigensCD8-Positive T-LymphocytesHumansPrognosisTranscription FactorsB7 AntigensCD68 antigen, humanCD68 MoleculeCD8 AntigensTranscription FactorsVSIR protein, humanbiomarkerCD68CD8pancreatic ductal adenocarcinomaPDACprognosisVISTA

Identifiers

PMID38357542
PMCPMC10865497
OpenAlexW4391359086

What OpenQuestion holds

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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.