Journal article

Quantitative Plasma Proteomics to Identify Candidate Biomarkers of Relapse in Pediatric/Adolescent Hodgkin Lymphoma


Authors listRepetto, Ombretta; Caggiari, Laura; De Zorzi, Mariangela; Elia, Caterina; Mussolin, Lara; Buffardi, Salvatore; Pillon, Marta; Muggeo, Paola; Casini, Tommaso; Steffan, Agostino; Mauz-Koerholz, Christine; Mascarin, Maurizio; De Re, Valli

Publication year2022

JournalInternational Journal of Molecular Sciences

Volume number23

Issue number17

ISSN1661-6596

eISSN1422-0067

Open access statusGold

DOI Linkhttps://doi.org/10.3390/ijms23179911

PublisherMDPI


Abstract
Classical pediatric Hodgkin Lymphoma (HL) is a rare malignancy. Therapeutic regimens for its management may be optimized by establishing treatment response early on. The aim of this study was to identify plasma protein biomarkers enabling the prediction of relapse in pediatric/adolescent HL patients treated under the pediatric EuroNet-PHL-C2 trial. We used untargeted liquid chromatography-tandem mass spectrometry (LC-MS/MS)-based proteomics at the time of diagnosis-before any therapy-as semiquantitative method to profile plasma proteins specifically associated with relapse in 42 children with nodular sclerosing HL. In both the exploratory and the validation cohorts, six proteins (apolipoprotein E, C4b-binding protein alpha chain, clusterin, fibrinogen gamma chain, prothrombin, and vitronectin) were more abundant in the plasma of patients whose HL relapsed (vertical bar fold change vertical bar >= 1.2, p < 0.05, Student's t-test). Predicting protein function with the Gene Ontology classification model, the proteins were included in four biological processes (p < 0.01). Using immunoblotting and Luminex assays, we validated two of these candidate biomarkers-C4b-binding protein alpha chain and clusterin-linked to innate immune response function (GO:0045087). This study identified C4b-binding protein alpha chain and clusterin as candidate early plasma biomarkers of HL relapse, and important for the purpose of shedding light on the molecular scenario associated with immune response in patients treated under the EuroNet-PHL-C2 trial.



Citation Styles

Harvard Citation styleRepetto, O., Caggiari, L., De Zorzi, M., Elia, C., Mussolin, L., Buffardi, S., et al. (2022) Quantitative Plasma Proteomics to Identify Candidate Biomarkers of Relapse in Pediatric/Adolescent Hodgkin Lymphoma, International Journal of Molecular Sciences, 23(17), Article 9911. https://doi.org/10.3390/ijms23179911

APA Citation styleRepetto, O., Caggiari, L., De Zorzi, M., Elia, C., Mussolin, L., Buffardi, S., Pillon, M., Muggeo, P., Casini, T., Steffan, A., Mauz-Koerholz, C., Mascarin, M., & De Re, V. (2022). Quantitative Plasma Proteomics to Identify Candidate Biomarkers of Relapse in Pediatric/Adolescent Hodgkin Lymphoma. International Journal of Molecular Sciences. 23(17), Article 9911. https://doi.org/10.3390/ijms23179911



Keywords


B-CELLSC4B-BINDING PROTEINC4b-binding protein alpha chainCD40clusterinCLUSTERIN EXPRESSIONLABELlabel-free quantificationpediatric Hodgkin LymphomaRELAPSE

Last updated on 2025-10-06 at 11:44