4.7 Article

Proteomic Landscape of Extracellular Vesicles for Diffuse Large B-Cell Lymphoma Subtyping

期刊

出版社

MDPI
DOI: 10.3390/ijms222011004

关键词

extracellular vesicles; exosomes; DLBCL; diffuse large B-cell lymphoma; proteomics; mass spectrometry

资金

  1. Fundacao para a Ciencia e a Tecnologia
  2. Lisboa Portugal Regional Operational Programme (Lisboa2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF) [iNOVA4Health-UIDB/04462/2020]
  3. FEDER funds through the COMPETE 2020 Programme
  4. National Funds through FCT-Portuguese Foundation for Science and Technology [PTDC/BTMTEC/30087/2017, PTDC/BTM-TEC/30088/2017]
  5. Champalimaud Foundation
  6. EMBO Installation Grant [3921]
  7. Fundação para a Ciência e a Tecnologia [PTDC/BTM-TEC/30088/2017] Funding Source: FCT

向作者/读者索取更多资源

The study analyzed the proteome of EVs in DLBCL subtypes and found that they can effectively separate cells into GCB and ABC categories. Through functional and enrichment analysis, it was discovered that DEPs are significantly enriched in immune response pathways, suggesting the potential of using EVs as diagnostic and therapeutic tools.
The role of extracellular vesicles (EVs) proteome in diffuse large B-cell lymphoma (DLBCL) pathology, subclassification, and patient screening is unexplored. We analyzed by state-of-the-art mass spectrometry the whole cell and secreted extracellular vesicles (EVs) proteomes of different molecular subtypes of DLBCL, germinal center B cell (GCB subtype), and activated B cell (ABC subtype). After quality control assessment, we compared whole-cell and secreted EVs proteomes of the two cell-of-origin (COO) categories, GCB and ABC subtypes, resulting in 288/1115 significantly differential expressed proteins from the whole-cell proteome and 228/608 proteins from EVs (adjust p-value < 0.05/p-value < 0.05). In our preclinical model system, we demonstrated that the EV proteome and the whole-cell proteome possess the capacity to separate cell lines into ABC and GCB subtypes. KEGG functional analysis and GO enrichment analysis for cellular component, molecular function, and biological process of differential expressed proteins (DEP) between ABC and GCB EVs showed a significant enrichment of pathways involved in immune response function. Other enriched functional categories for DEPs constitute cellular signaling and intracellular trafficking such as B-cell receptor (BCR), Fc_gamma R-mediated phagocytosis, ErbB signaling, and endocytosis. Our results suggest EVs can be explored as a tool for patient diagnosis, follow-up, and disease monitoring. Finally, this study proposes novel drug targets based on highly expressed proteins, for which antitumor drugs are available suggesting potential combinatorial therapies for aggressive forms of DLBCL.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据