# Netrin‐1 and B‐cell maturation antigen expression in a large cohort of 361 lymphomas: sensitive and specific staining in plasmablastic lymphomas, and therapeutic perspectives

**Authors:** Marie Donzel, Alexis Trecourt, Hervé Ghesquières, Thi‐Thuy‐Trinh Nguyen, Sara Dandash, Morgane Denis, Emeline Cros‐Perrial, Juliette Fontaine, Charles Dumontet, Alexandra Traverse‐Glehen

PMC · DOI: 10.1002/2056-4538.70027 · The Journal of Pathology: Clinical Research · 2025-04-15

## TL;DR

This study examines Netrin-1 and BCMA in lymphomas, finding high expression in plasmablastic lymphomas, suggesting potential for diagnosis and therapy.

## Contribution

The study provides a comprehensive analysis of Netrin-1 and BCMA expression in a large lymphoma cohort, highlighting their diagnostic and therapeutic potential.

## Key findings

- Netrin-1 showed 96% sensitivity and 100% specificity in plasmablastic lymphomas.
- BCMA exhibited 85% sensitivity and 95% specificity in plasmablastic lymphomas.
- Netrin-1 and BCMA expression was rare in other lymphoma subtypes.

## Abstract

Netrin‐1 and B‐cell maturation antigen (BCMA) are currently being evaluated as therapeutic targets in oncology. However, studies investigating their expression in mature human lymphoid malignancies are sparse. This study aimed to investigate the expression of BCMA and Netrin‐1 in a large cohort of lymphomas to determine their potential role as biomarkers or therapeutic targets. BCMA and Netrin‐1 expression was investigated comprehensively using immunohistochemistry in a cohort that included 261 B‐cell lymphomas, 45 T‐cell lymphomas, and 55 classical Hodgkin lymphomas. Netrin‐1 displayed a cytoplasmic staining pattern in plasmablastic lymphomas (27/28, 96%) and classical Hodgkin lymphomas (8/55, 15%). BCMA displayed cytoplasmic staining in most plasmablastic lymphomas (17/20, 85%). Among mature B‐cell lymphomas, Netrin‐1 and BCMA displayed sensitive (96% and 85%, respectively) and specific (100% and 95%, respectively) staining in plasmablastic lymphomas. These results suggest that these proteins may help pathologists in complex diagnoses and reinforce the interest in developing clinical trials assessing Netrin‐1 or BCMA‐targeted therapies in plasmablastic lymphoma and classical Hodgkin lymphomas, for which our therapeutic arsenal is weak.

## Linked entities

- **Proteins:** Ntn1 (netrin 1), TNFRSF17 (TNF receptor superfamily member 17)
- **Diseases:** plasmablastic lymphoma (MONDO:0017347), classical Hodgkin lymphoma (MONDO:0009348), B-cell lymphoma (MONDO:0015759), T-cell lymphoma (MONDO:0015760)

## Full-text entities

- **Genes:** TNFRSF17 (TNF receptor superfamily member 17) [NCBI Gene 608] {aka BCM, BCMA, CD269, TNFRSF13A}, NTN1 (netrin 1) [NCBI Gene 9423] {aka MRMV4, NET1, NTN1L}
- **Diseases:** B-cell lymphomas (MESH:D016393), lymphoid malignancies (MESH:D008223), plasmablastic lymphoma (MESH:D000069293), classical Hodgkin lymphomas (MESH:D006689), T-cell lymphomas (MESH:D016399)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12000542/full.md

## References

26 references — full list in the complete paper: https://tomesphere.com/paper/PMC12000542/full.md

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Source: https://tomesphere.com/paper/PMC12000542