Evidence map›Paper›PMID 38028180›Full record

ArticleOncology letters2024

Effect of IFN‑γ encapsulated liposomes on major signal transduction pathways in the lymphocytes of patients with lung cancer.

Maysa Alhawamdeh, Belal Almajali, Wafa Hourani, Hamid Ali Nagi Al-Jamal, Abdullah Saleh Al-Wajeeh, Nesrin Riad Mwafi, Yousef Al-Hajaya, Hanan Kamel M Saad, Diana Anderson, Mahmoud Odeh and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 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
1.4field-weighted citation impact, top 15% 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

2 citing papers in PubMed, 6 citations in OpenAlex.

  1. 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

11 authors at 8 institutions in 4 countries.

Maysa AlhawamdehDepartment of Medical Laboratory Sciences, Faculty of Allied Medical Sciences, Mutah University, Al-Karak 61710, Jordan.
Belal AlmajaliDepartment of Medical Laboratory Science, Faculty of Allied Medical Sciences, Al-Ahliyya Amman University, Amman 19111, Jordan.
Wafa HouraniFaculty of Pharmacy, Philadelphia University, Amman 19392, Jordan.
Hamid Ali Nagi Al-JamalSchool of Biomedicine, Faculty of Health Sciences, Universiti Sultan Zainal Abidin, Kuala Nerus, Terengganu 21300, Malaysia.
Abdullah Saleh Al-WajeehMetabolomics Department, Anti-Doping Lab Qatar, Doha 27775, Qatar.
Nesrin Riad MwafiDepartment of Biochemistry and Molecular Biology, Faculty of Medicine, Mutah University, Al-Karak 61710, Jordan.
Yousef Al-HajayaDepartment of Medical Laboratory Sciences, Faculty of Allied Medical Sciences, Mutah University, Al-Karak 61710, Jordan.
Hanan Kamel M SaadSchool of Biomedicine, Faculty of Health Sciences, Universiti Sultan Zainal Abidin, Kuala Nerus, Terengganu 21300, Malaysia.
Diana AndersonDivision of Medical Sciences, Faculty of Life Sciences, University of Bradford, Bradford, BD7 1DP, UK.
Mahmoud OdehBusiness Faculty, Zarqa University, Zarqa 13110, Jordan.
Ibraheam A TarawnehSchool of Graduate Studies, Management and Science University, Shah Alam, Selangor 40100, Malaysia.
Mutah University · JOSultan Zainal Abidin University · MYAl-Ahliyya Amman University · JOAnti-Doping Laboratory · QAManagement and Science University · MYPhiladelphia University · JOUniversity of Bradford · GBZarqa University · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Globally, lung cancer affected 2.2 million individuals and caused 1.8 million deaths in 2021. Lung cancer is caused by smoking, genetics and other factors. IFN-γ has anticancer activity. However, the mechanism by which IFN-γ has an effect on lung cancer is not fully understood. The present study aimed to assess the effect of IFN-γ on the peripheral lymphocytes of patients with lung cancer compared with healthy controls. The efficacy of IFN-γ against oxidative stress was assessed using a comet repair assay and the effects of IFN-γ on p53, PARP1 and OGG1 genes and protein levels in lymphocytes was evaluated by RT-qPCR and western blotting. DNA damage was significantly reduced in the lymphocytes of patients treated with IFN-γ. However, there was no effect in the cells of healthy individuals after treatment with naked IFN-γ [IFN-γ (N)] and liposomal IFN-γ [IFN-γ (L)]. Following treatment with IFN-γ (N) and IFN-γ (L), the p53, PARP1 and OGG1 protein and gene expression levels were significantly increased (P<0.001). It has been suggested that IFN-γ may induce p53-mediated cell cycle arrest and DNA repair in patients. These findings supported the idea that IFN-γ (N) and IFN-γ (L) may serve a significant role in the treatment of lung cancer, via cell cycle arrest of cancer cells and repair mechanisms.

Indexed as

IFN-γliposomesLung cancerlymphocytesOGG1p53PARP1

Identifiers

PMID38028180
PMCPMC10664063
OpenAlexW4388553776

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.