Role Of Neuron-Specific Enolase and Ferritin in Neuroblastoma and Wilms Tumor
Keywords:
neuron-specific enolase, ferritin, neuroblastoma, wilms tumorAbstract
The role of enolase isozymes and ferritin as biomarkers in pediatric solid tumors, including neuroblastoma and Wilms tumor. While neuron-specific enolase (NSE) is well-established in neuroendocrine tumors, its expression patterns and prognostic significance in other childhood cancers remain underexplored. Similarly, ferritin, traditionally linked to iron metabolism and inflammation, may have unrecognized associations with tumor aggressiveness or treatment response in these malignancies. dysregulated enolase isoforms and altered ferritin levels correlate with disease progression, metastatic potential, or therapeutic outcomes in pediatric solid tumors. Patient and methods: This case-control study, conducted at Baghdad Teaching Hospital (February–December 2024), evaluated Neuron-Specific Enolase (NSE) and ferritin as potential biomarkers in pediatric solid tumors. The study included 98 children under 10 years old, divided into three groups: 34 neuroblastoma patients, 31 Wilms tumor patients, and 33 healthy controls. Serum levels of NSE and ferritin were measured using Sandwich ELISA. This case-control study evaluated serum neuron-specific enolase (NSE) and ferritin levels in pediatric solid tumors. Neuroblastoma patients exhibited dramatically elevated NSE (424.71±326.17 ng/mL; 43-fold higher than controls, p<0.001) and significantly higher levels than Wilms tumor cases (175.45±97.41 ng/mL, p<0.001). Conversely, Wilms tumor patients showed the highest ferritin levels (505.84±266.58 μg/L; 7.9-fold above controls, p<0.001), significantly exceeding neuroblastoma values (324.12±138.11 μg/L, p<0.001). These findings demonstrate distinct biomarker profiles: NSE shows exceptional elevation in neuroblastoma, while ferritin is markedly increased in Wilms tumor, suggesting their potential diagnostic utility in differentiating these pediatric malignancies
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Zimmermann E, Berentzen TL, Gamborg M, Sørensen TIA, Baker JL. Sex‐specific associations between birth weight and adult primary liver cancer in a large cohort of D anish children. Int J Cancer. 2016;138(6):1410–5.
Höllwarth ME. Wilms’ tumor. In: Pediatric surgery: diagnosis and management. Springer; 2023. p. 673–84.
de Carvalho LG, Kobayashi T, Cypriano M dos S, Caran EMM, Lederman HM, Alves MT de S, et al. Diagnostic errors in Wilms’ tumors: Learning from our mistakes. Front Pediatr. 2021;9:757377.
Gupta DK, Sharma S, Agarwala S, Carachi R. Saga of Wilms’ tumor: lessons learnt from the past. J Indian Assoc Pediatr Surg. 2005;10(4):217–28.
Horvat S, Kos J, Pišlar A. Multifunctional roles of γ-enolase in the central nervous system: more than a neuronal marker. Cell Biosci. 2024;14(1):61.
Faridova AT, Heřman H, Danačíková Š, Svoboda J, Otahal J. Serum biomarkers of hypoxic-ischemic brain injury. Physiol Res. 2023;72(Suppl 5):S461.
Class IPC, USPC A. Patent application title: Dopamine Receptor Agonists in the Treatment and Prevention of Hiv-Induced Dementia Inventors: Rosemarie M. Booze (Columbia, SC, US) Charles Mactutus (Columbia, SC, US). 2008;
Wajdi Ibrahim W, Talib Mosa M. The Role of Acute Phase Reactants (Fibrinogen, Ferritin, Albumin, Calcium) in Pregnant Women with Preterm Delivery. J Fac Med Baghdad [Internet]. 2022;64(3):133–8. Available from: https://doi.org/10.32007/jfacmedbagdad.6431943
Al-Rubaie HA, Hasan DD, Al-Rubaye RA. Classification of anemia in hemodialysis patients in relation to vascular access and its correlation with hepcidin and ferritin. J Fac Med Baghdad [Internet]. 2016;58(2):159–64. Available from: https://doi.org/10.32007/jfacmedbagdad.582232
A. Abdul Hussein Z, AL-Obaidy MWS, M. Hashim T, Al-Khairalla M. The Severity of COVID-19 in Patients with Hematological and Solid Malignancies: a Sample from Medical City in Baghdad. J Fac Med Baghdad [Internet]. 2024;66(1):1–10. Available from: https://doi.org/10.32007/jfacmedbagdad.6612086
Blatt J, Huntley D, Eagon PK. Synthesis of ferritin by neuroblastoma. Cancer Biochem Biophys. 1990 Apr;11(2):169–76.
Imashuku S, Yamanaka H, Morioka Y, Todo S. Serum ferritin in stage IV neuroblastoma. Am J Pediatr Hematol Oncol. 1988;10(1):39–41.
Hann HW, Stahlhut MW, Evans AE. Basic and acidic isoferritins in the sera of patients with neuroblastoma. Cancer. 1988 Sep;62(6):1179–82.
Iancu TC, Shiloh H, Kedar A. Neuroblastomas contain iron-rich ferritin. Cancer. 1988 Jun;61(12):2497–502.
Wei W. Ferritin involved in the tumor development. Chinese-German J Clin Oncol [Internet]. 2013;12(11):551–4. Available from: https://doi.org/10.1007/s10330-013-1237-4
Alkhateeb A, Leitzel K, Lipton A, Connor J. EXTRACELLULAR FERRITIN IS A TUMORIGENIC FACTOR AND IS SECRETED BY TUMOR-ASSOCIATED MACROPHAGES: A FUNCTIONAL LINK BETWEEN INFLMATION AND TUMORIGENESIS. Am J Hematol. 2013 May 1;88:E16–7.
Deng G, Li Y, Liang N, Hu P, Zhang Y, Qiao L, et al. Ferritin in cancer therapy: A pleiotropic tumoraffin nanocage-based transport. Cancer Med. 2023 May;12(10):11570–88.
Fan K, Gao L, Yan X. Human ferritin for tumor detection and therapy. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2013;5(4):287–98.
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