Card
Series GSE240252 Query DataSets for GSE240252
Status Public on Oct 24, 2024
Title Single-cell transcriptomics of pediatric Burkitt lymphoma
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary Burkitt lymphoma (BL) is the most frequent B-cell lymphoma in pediatric patients. While most patients are currently cured, a fraction of them are resistant to therapy. In order to investigate BL heterogeneity and the features distinguishing the non-responders (NR) to therapy, we analyzed pediatric EBV-negative BL specimens collected at diagnosis by single-cell (sc)-transcriptomics. Analysis of the non-tumor component revealed a predominance of immune cell infiltrates and a small representation of fibroblasts that was enriched in NR. Tumor cells displayed patient-specific features, as well as subpopulations that were common to most patients and expressed transcripts related to cell cycle, signaling pathways and cell-of-origin signatures.
 
Overall design Paired single-cell transcriptomics and immunoglobulin repertoire analyses were performed on 12 sporadic EBV-negative BL specimens (11 patients), including 8 pleural or abdominal effusions and 4 nodal tumor masses, which were collected at diagnosis and frozen as viable single cell suspensions.
 
Contributor(s) Basso K, Holmes AB, Mussolin L, Dalla-Favera R
Citation(s)
  • Corinaldesi C, Holmes AB, Martire G, Tosato A et al. Single-cell transcriptomics of pediatric Burkitt lymphoma reveals intra-tumor heterogeneity and markers of therapy resistance. Leukemia 2025 Jan;39(1):189-198. PMID: 39424708
Submission date Aug 07, 2023
Last update date Oct 24, 2024
Contact name Riccardo Dalla-Favera
E-mail(s) rd10@cumc.columbia.edu
Organization name Columbia University
Street address 1130 St Nicholas Avenue
City New York
State/province NY
ZIP/Postal code 10032
Country USA
 
Platforms (1)
GPL24676 Illumina NovaSeq 6000 (Homo sapiens)