Evidence map›Paper›PMID 39361074›Full record

ArticleMolecular biology reports2024

Assessment of the circulating levels of immune system checkpoint selected biomarkers in patients with lung cancer.

Banafsheh Safizadeh, Maryam Sadeh, Ali Karami Robati, Taghi Riahi, Masoumeh Tavakoli-Yaraki

Abstract read
PubMed Publisher
In one paragraph

Article in Molecular biology reports, 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

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

2 citing papers in PubMed.

  1. Development and validation of a transformer-based deep learning model for predicting distant metastasis in non-small cell lung cancer usingClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  2. 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

5 authors.

Banafsheh SafizadehDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, P.O. Box: 1449614535, Tehran, Iran.
Maryam SadehDepartment of Internal Medicine, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Ali Karami RobatiDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, P.O. Box: 1449614535, Tehran, Iran.
Taghi RiahiDepartment of Internal Medicine, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Masoumeh Tavakoli-YarakiDepartment of Biochemistry, School of Medicine, Iran University of Medical Sciences, P.O. Box: 1449614535, Tehran, Iran. tavakoli.m@iums.ac.ir.ORCID https://orcid.org/0000-0003-4449-9248

Funding

Iran University of Medical Sciences 1400-1-4-19493
6 · The paper itself

Abstract

backgroundLung cancer is recognized as one of the leading causes of cancer-related deaths globally, with a significant increase in incidence and intricate pathogenic mechanisms. This study examines the expression profiles of Programmed Cell Death Protein 1 (PD-1), PD-1 ligand (PDL-1), β-catenin, CD44, interleukin 6 (IL-6), and interleukin 10 (IL-10), as well as their correlations with the clinic-pathological features and diagnostic significance in lung cancer patients. METHODS AND

resultsThe research involved lung cancer patients exhibiting various pathological characteristics, alongside demographically matched healthy controls. The expression levels of PD-1, PDL-1, β-catenin, and CD44 were analyzed using Real-Time PCR, while circulating levels of IL-6 and IL-10 were assessed through ELISA assays. This investigation focused on peripheral blood mononuclear cells (PBMC) to evaluate these factors non-invasively. Findings indicated that levels of PD-1, PDL-1, and CD44 were significantly elevated in patients compared to controls, which coincided with a decrease in β-catenin levels. Additionally, a concurrent rise in IL-6 and IL-10, both pro-inflammatory cytokines, was observed in patients, suggesting a potential regulatory role for these cytokines on the PD-1/PDL-1 axis, which may help tumors evade immune system checkpoints. The predictive value of these factors concerning lung tumors and metastasis was significant (Regression analysis). Furthermore, these markers demonstrated diagnostic potential in differentiating between patients and healthy controls, as well as between individuals with metastatic and non-metastatic tumors (ROC curve analysis).

conclusionsThis study provides insights into the expression profiles of PD-1/PDL-1 immune system checkpoints and their regulatory factors in lung cancer, potentially paving the way for new therapeutic and diagnostic approaches.

Indexed as

B7-H1 Antigenbeta CateninBiomarkers, TumorHyaluronan ReceptorsInterleukin-10Interleukin-6Lung NeoplasmsProgrammed Cell Death 1 ReceptorAdultAgedCase-Control StudiesFemaleHumansImmune Checkpoint ProteinsLeukocytes, MononuclearMaleB7-H1 Antigenbeta CateninBiomarkers, TumorCD274 protein, humanCD44 protein, humanCTNNB1 protein, humanHyaluronan ReceptorsIL10 protein, humanImmune Checkpoint ProteinsInterleukin-10Interleukin-6PDCD1 protein, humanProgrammed Cell Death 1 ReceptorCD44Interleukin 10Interleukin 6Lung cancerPD-1PDL-1Β-catenin

Identifiers

What OpenQuestion 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 OpenQuestion graph.