Single-cell transcriptomics of pediatric Burkitt lymphoma reveals intra-tumor heterogeneity and markers of therapy resistance

Burkitt lymphoma (BL) is the most frequent B-cell lymphoma in pediatric patients. While most patients are cured, a fraction of them are resistant to therapy. To investigate BL heterogeneity and the features distinguishing therapy responders (R) from non-responders (NR), we analyzed by single-cell (sc)-transcriptomics diagnostic EBV-negative BL specimens. Analysis of the non-tumor component revealed a predominance of immune cells and a small representation of fibroblasts, enriched in NR. Tumors displayed patient-specific features, as well as shared subpopulations that expressed transcripts related to cell cycle, signaling pathways and cell-of-origin signatures. Several transcripts were differentially expressed in R versus NR. The top candidate, Tropomyosin 2 (TPM2), a member of the tropomyosin actin filament binding protein family, was confirmed to be significantly higher in NR both at the transcript and protein level. Stratification of patients based on TPM2 expression at diagnosis significantly correlated with prognosis, independently of TP53 mutations. These results indicate that BL displays transcriptional heterogeneity and identify candidate biomarkers of therapy resistance.

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Publication Details

Journal
Leukemia
Published
2024-10-18
DOI
https://doi.org/10.1038/s41375-024-02431-3
Citations
8
Primary Topic
Lymphoma Diagnosis and Treatment
Type
article
Field-Weighted Citation Impact
3.40

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article

Single-cell transcriptomics of pediatric Burkitt lymphoma reveals intra-tumor heterogeneity and markers of therapy resistance

Kenneth Ofori, Govind Bhagat, Roberto Chiarle, Antony B. Holmes et al.
8 citations
Leukemia
Lymphoma Diagnosis and Treatment
3.40
article

Single-cell transcriptomics of pediatric Burkitt lymphoma reveals intra-tumor heterogeneity and markers of therapy resistance

Kenneth Ofori, Govind Bhagat, Roberto Chiarle, Antony B. Holmes, Shafinaz Hussein, Angelo Paolo Dei Tos, Ilaria Gallingani, Emanuele S. G. d'Amore, Marian H. Harris, Umberto Mortara, Lara Mussolin, Elisa Carraro, Federica Lovisa, Anna Tosato, Qiong Shen, Lavinia Ferrone, Luca Molinaro, Katia Basso, Clarissa Corinaldesi, Marco Pizzi, Marta Pillon, Gaia Martire, Domenico Rizzato, Bo Ngan, Kimberly Davies
article en
8 citations

Abstract

Burkitt lymphoma (BL) is the most frequent B-cell lymphoma in pediatric patients. While most patients are cured, a fraction of them are resistant to therapy. To investigate BL heterogeneity and the features distinguishing therapy responders (R) from non-responders (NR), we analyzed by single-cell (sc)-transcriptomics diagnostic EBV-negative BL specimens. Analysis of the non-tumor component revealed a predominance of immune cells and a small representation of fibroblasts, enriched in NR. Tumors displayed patient-specific features, as well as shared subpopulations that expressed transcripts related to cell cycle, signaling pathways and cell-of-origin signatures. Several transcripts were differentially expressed in R versus NR. The top candidate, Tropomyosin 2 (TPM2), a member of the tropomyosin actin filament binding protein family, was confirmed to be significantly higher in NR both at the transcript and protein level. Stratification of patients based on TPM2 expression at diagnosis significantly correlated with prognosis, independently of TP53 mutations. These results indicate that BL displays transcriptional heterogeneity and identify candidate biomarkers of therapy resistance.

LeukemiaVol. 39(1)
Boston Children's Hospital (US), Harvard University (US), University of Padua (IT), Columbia University Irving Medical Center (US), Dana-Farber Cancer Institute (US), SickKids Foundation (CA), Cancer Genetics (United States) (US), Ospedale San Bortolo (IT), Città della Speranza Foundation (IT), University of Turin (IT), European Institute of Oncology (IT), Columbia University (US), Icahn School of Medicine at Mount Sinai (US)
Lymphoma Research Foundation, Fondazione Città della Speranza, National Institutes of Health, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 7%
Lymphoma Diagnosis and Treatment
3.40
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