Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt

Abstract Evading apoptosis fuels the aggressive nature of acute lymphoblastic leukemia (ALL). This study explored the potential roles of TNF-α, a pro-apoptotic cytokine, and TGF-β, a pro-proliferative factor, in the risk of developing ALL in Egyptian children. We investigated the TNF-α rs1800629 pol...

Full description

Saved in:
Bibliographic Details
Main Authors: Roqaia E. Radwan, Wafaa M. El-kholy, Afaf Elsaed, Ahmad Darwish
Format: Article
Language:English
Published: BMC 2024-12-01
Series:BMC Cancer
Subjects:
Online Access:https://doi.org/10.1186/s12885-024-13224-3
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1846121819907555328
author Roqaia E. Radwan
Wafaa M. El-kholy
Afaf Elsaed
Ahmad Darwish
author_facet Roqaia E. Radwan
Wafaa M. El-kholy
Afaf Elsaed
Ahmad Darwish
author_sort Roqaia E. Radwan
collection DOAJ
description Abstract Evading apoptosis fuels the aggressive nature of acute lymphoblastic leukemia (ALL). This study explored the potential roles of TNF-α, a pro-apoptotic cytokine, and TGF-β, a pro-proliferative factor, in the risk of developing ALL in Egyptian children. We investigated the TNF-α rs1800629 polymorphism and serum TGF-β levels in 100 ALL patients and 100 healthy controls. Notably, specific variations in TNF-α (GA, AA genotypes, and dominant model) were associated with an increased risk of ALL, suggesting impaired apoptosis. Conversely, ALL patients exhibited significantly lower TGF-β levels, potentially promoting uncontrolled proliferation. Our findings suggest that lower TGF-β and the TNF-α (-308) dominant model are associated with an increased risk of ALL. Additionally, TGF-β demonstrated exceptional accuracy (AUC 0.995) as a potential marker, with 100% sensitivity and 96% specificity. These findings suggest that TNF-α and TGF-β may be associated with ALL susceptibility, though further research with larger and more diverse populations is necessary to confirm these results.
format Article
id doaj-art-c9a14cea39e04c1e91366b6ccce72bcf
institution Kabale University
issn 1471-2407
language English
publishDate 2024-12-01
publisher BMC
record_format Article
series BMC Cancer
spelling doaj-art-c9a14cea39e04c1e91366b6ccce72bcf2024-12-15T12:09:32ZengBMCBMC Cancer1471-24072024-12-0124111310.1186/s12885-024-13224-3Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in EgyptRoqaia E. Radwan0Wafaa M. El-kholy1Afaf Elsaed2Ahmad Darwish3Physiology Section, Zoology Department, Faculty of Science, Mansoura UniversityPhysiology Section, Zoology Department, Faculty of Science, Mansoura UniversityGenetics Unit, Children Hospital, Mansoura UniversityHematology, Oncology and Bone Marrow Transplantation Unit, Pediatric Department, Faculty of Medicine, Mansoura UniversityAbstract Evading apoptosis fuels the aggressive nature of acute lymphoblastic leukemia (ALL). This study explored the potential roles of TNF-α, a pro-apoptotic cytokine, and TGF-β, a pro-proliferative factor, in the risk of developing ALL in Egyptian children. We investigated the TNF-α rs1800629 polymorphism and serum TGF-β levels in 100 ALL patients and 100 healthy controls. Notably, specific variations in TNF-α (GA, AA genotypes, and dominant model) were associated with an increased risk of ALL, suggesting impaired apoptosis. Conversely, ALL patients exhibited significantly lower TGF-β levels, potentially promoting uncontrolled proliferation. Our findings suggest that lower TGF-β and the TNF-α (-308) dominant model are associated with an increased risk of ALL. Additionally, TGF-β demonstrated exceptional accuracy (AUC 0.995) as a potential marker, with 100% sensitivity and 96% specificity. These findings suggest that TNF-α and TGF-β may be associated with ALL susceptibility, though further research with larger and more diverse populations is necessary to confirm these results.https://doi.org/10.1186/s12885-024-13224-3ALLTNF-alphaTGF-betaSNPsCytokine levels
spellingShingle Roqaia E. Radwan
Wafaa M. El-kholy
Afaf Elsaed
Ahmad Darwish
Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt
BMC Cancer
ALL
TNF-alpha
TGF-beta
SNPs
Cytokine levels
title Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt
title_full Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt
title_fullStr Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt
title_full_unstemmed Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt
title_short Genetic predisposition meets cytokine imbalance: the influence of TNF-α (-308) polymorphism and TGF-β levels in pediatric acute lymphoblastic leukemia in Egypt
title_sort genetic predisposition meets cytokine imbalance the influence of tnf α 308 polymorphism and tgf β levels in pediatric acute lymphoblastic leukemia in egypt
topic ALL
TNF-alpha
TGF-beta
SNPs
Cytokine levels
url https://doi.org/10.1186/s12885-024-13224-3
work_keys_str_mv AT roqaiaeradwan geneticpredispositionmeetscytokineimbalancetheinfluenceoftnfa308polymorphismandtgfblevelsinpediatricacutelymphoblasticleukemiainegypt
AT wafaamelkholy geneticpredispositionmeetscytokineimbalancetheinfluenceoftnfa308polymorphismandtgfblevelsinpediatricacutelymphoblasticleukemiainegypt
AT afafelsaed geneticpredispositionmeetscytokineimbalancetheinfluenceoftnfa308polymorphismandtgfblevelsinpediatricacutelymphoblasticleukemiainegypt
AT ahmaddarwish geneticpredispositionmeetscytokineimbalancetheinfluenceoftnfa308polymorphismandtgfblevelsinpediatricacutelymphoblasticleukemiainegypt