Evidence map›Paper›PMID 42683370›Full record

ArticleIranian journal of basic medical sciences2026

Modulation of CCL5 and CXCR4 as EMT signaling biomarkers by cold atmospheric plasma and Anti-PD-1 combination therapy in melanoma: Insights from integrated bioinformatics and

Zeinab Rostami, Fatemeh Akhoundi, Zahra Yazdani, Mohammad Eslamijouybari, Mansooreh Mirzaei, Forouzan Bousaeedi, Ghazaleh Rostami, Alireza Rafiei

Abstract read
In one paragraph

Article in Iranian journal of basic medical sciences, 2026. 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
–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

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.

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

8 authors.

Zeinab RostamiDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Fatemeh AkhoundiDepartment of Genetics, Faculty of Basic Sciences, Shahrekord University, Shahrekord, Iran.
Zahra YazdaniDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Mohammad EslamijouybariGastrointestinal Cancer Research Center, Non-Communicable Diseases Institute, Mazandaran University of Medical Sciences, Sari, Iran.
Mansooreh MirzaeiDepartment of Anatomy, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Forouzan BousaeediDepartment of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Ghazaleh RostamiStudent Research Committee, School of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Alireza RafieiDepartment 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

Objectives: Cold atmospheric plasma (CAP) has emerged as a promising non-thermal modality with anticancer effects. Combining CAP with immune checkpoint blockade (ICB) may enhance therapeutic efficacy, yet the molecular targets underlying this synergy remain incompletely understood. Materials and Methods: Epithelial--mesenchymal transition (EMT)--associated genes responsive to CAP and Anti-PD-1 therapy were identified by integrating bioinformatics analyses of melanoma transcriptomic data with Results: WGCNA highlighted CCL5 and CXCR4 as hub genes enriched in EMT-related pathways. MTT assays showed that CAP reduced B16F10 cell viability, an effect further enhanced by Anti-PD-1, while sparing L929 fibroblasts. In tumor-bearing mice, combination therapy produced the most pronounced tumor regression and down-regulation of CCL5 and CXCR4 compared with single treatments. Minimal viability or expression changes were observed in normal fibroblasts or untreated controls. Conclusion: CAP and Anti-PD-1 combination therapy effectively suppressed melanoma cell viability and modulated EMT-associated gene expression both

Indexed as

Anti-PD-1C-C motif chemokine ligand - 5 (CCL5)Cold atmospheric plasma - (CAP)C-X-C chemokine receptor - type 4 (CXCR4)Epithelial-mesenchymal - transition (EMT)Melanoma

Identifiers

PMID42683370
PMCPMC13531678

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.