弥漫性大B细胞淋巴瘤B细胞单细胞转录组数据集

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• 源站标题：Table_2_Unraveling the enigma of B cells in diffuse large B-cell lymphoma: unveiling cancer stem cell-like B cell subpopulation at single-cell resolution.xlsx
• DOI：10.3389/fimmu.2023.1310292.s003
• 发布日期：2023-12-11
• 文件数：1 个
• 文件总体积：41.14 KB
• 源站页面：https://frontiersin.figshare.com/articles/dataset/Table_2_Unraveling_the_enigma_of_B_cells_in_diffuse_large_B-cell_lymphoma_unveiling_cancer_stem_cell-like_B_cell_subpopulation_at_single-cell_resolution_xlsx/24784515

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• Table_2_Unraveling the enigma of B cells in diffuse large B-cell lymphoma: unveiling cancer stem cell-like B cell subpopulation at single-cell resolut.xlsx（41.14 KB）

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数据说明

BackgroundDiffuse large B-cell lymphoma (DLBCL) represents the most prevalent form of aggressive non-Hodgkin lymphoma. Despite receiving standard treatment, a subset of patients undergoes refractory or recurrent cases, wherein the involvement of cancer stem cells (CSCs) could be significant.
MethodsWe comprehensively characterized B cell subpopulations using single-cell RNA sequencing data from three DLBCL samples and one normal lymph tissue. The CopyKat R package was employed to assess the malignancy of B cell subpopulations based on chromosomal copy number variations. CIBERSORTx software was utilized to estimate the proportions of B cell subpopulations in 230 DLBCL tissues. Furthermore, we employed the pySCENIC to identify key transcription factors that regulate the functionality of B cell subpopulations. By employing CellphoneDB, we elucidated the interplay among tumor microenvironment components within the B cell subpopulations. Finally, we validated our findings through immunofluorescence experiments.
ResultsOur analysis revealed a specific cancer stem cell-like B cell subpopulation exhibiting self-renewal and multilineage differentiation capabilities based on the exploration of B cell subpopulations in DLBCL and normal lymph tissues at the single-cell level. Notably, a high infiltration of cancer stem cell-like B cells correlated with a poor prognosis, potentially due to immune evasion mediated by low expression of major histocompatibility complex molecules. Furthermore, we identified key transcription factor regulatory networks regulated by HMGB3, SAP30, and E2F8, which likely played crucial roles in the functional characterization of the cancer stem cell-like B cell subpopulation. The existence of cancer stem cell-like B cells in DLBCL was validated through immunofluorescent staining. Finally, cell communication between B cells and tumor-infiltrating T cell subgroups provided further insights into the functional characterization of the cancer stem cell-like B cell subpopulation.
ConclusionsOur research provides a systematic description of a specific cancer stem cell-like B cell subpopulation associated with a poor prognosis in DLBCL. This study enhances

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引用

学术使用请引用 DOI 10.3389/fimmu.2023.1310292.s003（source: https://frontiersin.figshare.com/articles/dataset/Table_2_Unraveling_the_enigma_of_B_cells_in_diffuse_large_B-cell_lymphoma_unveiling_cancer_stem_cell-like_B_cell_subpopulation_at_single-cell_resolution_xlsx/24784515）。