FCRL1 and BAFF mRNA Expression as Novel Diagnostic and Prognostic Biomarkers in Diffuse Large B-Cell Lymphoma: Expression Signatures Predict R-CHOP Therapy Response and Survival

Int J Mol Sci. 2025 Jan 31;26(3):1269. doi: 10.3390/ijms26031269.

Abstract

This study investigated the diagnostic, prognostic, and therapeutic significance of Fc receptor-like 1 (FCRL1) and B-cell activating factor (BAFF) mRNA expression in Egyptian patients with diffuse large B-cell lymphoma (DLBCL) undergoing the standard R-CHOP regimen (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone) using quantitative real-time PCR (RT-qPCR). The results demonstrated that FCRL1 and BAFF mRNA expression were significantly elevated in DLBCL patients compared to healthy controls. A strong positive correlation existed between BAFF and FCRL1 expression levels. Diagnostic performance assessed through combined ROC curve analysis revealed that BAFF, FCRL1, and lactate dehydrogenase (LDH) achieved perfect diagnostic accuracy (AUC = 1.0), demonstrating 100% sensitivity, specificity, and predictive values. Further prognostic analysis using COX regression identified elevated FCRL1 expression as the most significant predictor of poor clinical outcomes. Kaplan-Meier survival analysis reinforced this finding, with high FCRL1 expression showing significant associations with reduced overall survival (OS, p = 0.031) and progression-free survival (PFS, p = 0.038). The study underscores the potential utility of BAFF and FCRL1 mRNA as diagnostic markers for DLBCL, with FCRL1 emerging as a promising prognostic marker and potential therapeutic target enabling more tailored treatment approaches for DLBCL, the most common type of B-cell non-Hodgkin lymphoma, and patients receiving R-CHOP therapy.

Keywords: B-cell non-Hodgkin lymphoma; BAFF; DLBCL; FCRL1; R-CHOP therapy; mRNA expression.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols* / therapeutic use
  • B-Cell Activating Factor* / genetics
  • B-Cell Activating Factor* / metabolism
  • Biomarkers, Tumor* / genetics
  • Cyclophosphamide* / therapeutic use
  • Doxorubicin* / therapeutic use
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Kaplan-Meier Estimate
  • Lymphoma, Large B-Cell, Diffuse* / diagnosis
  • Lymphoma, Large B-Cell, Diffuse* / drug therapy
  • Lymphoma, Large B-Cell, Diffuse* / genetics
  • Lymphoma, Large B-Cell, Diffuse* / mortality
  • Male
  • Middle Aged
  • Prednisone* / therapeutic use
  • Prognosis
  • RNA, Messenger* / genetics
  • RNA, Messenger* / metabolism
  • Receptors, Fc / genetics
  • Receptors, Fc / metabolism
  • Rituximab* / therapeutic use
  • Vincristine* / therapeutic use

Substances

  • Cyclophosphamide
  • Vincristine
  • Doxorubicin
  • Prednisone
  • Rituximab
  • R-CHOP protocol
  • B-Cell Activating Factor
  • Biomarkers, Tumor
  • RNA, Messenger
  • TNFSF13B protein, human
  • Receptors, Fc

Grants and funding

This research did not receive any specific grant from funding agencies.