Evidence map›Paper›PMID 39118076›Full record

ArticleBMC cancer2024

Exploring the potential of IL-10 for risk assessment and early intervention in pediatric ALL.

Roqaia E Radwan, Ahmad Darwish, Afaf M Elsaid, Wafaa M El-Kholy

Abstract read
In one paragraph

Article in BMC cancer, 2024. 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
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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

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

4 authors.

Roqaia E RadwanPhysiology Section, Zoology Department, Faculty of Science, Mansoura University, Mansoura, Egypt. rookas.ahmed@gmail.com.ORCID http://orcid.org/0009-0001-4619-8409
Ahmad DarwishHematology, Oncology and Bone Marrow Transplantation Unit, Pediatric Department, Faculty of Medicine, Mansoura University, Mansoura, Egypt.
Afaf M ElsaidGenetics Unit, Children Hospital, Mansoura University, Mansoura, Egypt.
Wafaa M El-KholyPhysiology Section, Zoology Department, Faculty of Science, Mansoura University, Mansoura, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute lymphoblastic leukemia (ALL), a leading cause of childhood cancer, targets immune system B and T cells. While understanding its causes is crucial, predicting susceptibility holds immense power for early diagnosis and intervention. This study explored the potential of interleukin 10 (IL-10), a key immune regulator, as a predictive tool in Egyptian children. Investigating 100 ALL patients and 100 healthy controls, we analyzed the IL10 gene polymorphism (-1082 A/G) and serum levels. Strikingly, both the G allele and higher serum IL-10 levels were significantly associated with increased ALL risk (p < 0.05, OR > 1). Moreover, IL-10 emerged as a remarkably accurate predictor, boasting an AUC of 0.995, with a sensitivity of 97% and specificity of 96%. These findings unveil the potential of IL-10 as a powerful predictive tool for pediatric ALL in the studied Egyptian population. Identifying individuals with the GG/AG haplotype and elevated IL-10 levels could enable early intervention and potentially improve outcomes. While further validation in larger and more diverse populations is needed, this study paves the way for personalized risk assessment and potentially revolutionizes how we combat this childhood killer.

Indexed as

Genetic Predisposition to DiseaseInterleukin-10Precursor Cell Lymphoblastic Leukemia-LymphomaAdolescentAllelesBiomarkers, TumorCase-Control StudiesChildChild, PreschoolEgyptFemaleGenotypeHumansInfantMalePolymorphism, Single NucleotideBiomarkers, TumorIL10 protein, humanInterleukin-10ALLCytokine levelsGene polymorphismIL10

Identifiers

PMID39118076
PMCPMC11308622

What Socratic holds

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LicenceCC BY
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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 Socratic graph.