EVmiRNA2.0: an updated database for miRNA expression in comprehensive human extracellular vesicles

Extracellular vesicle (EV)-derived microRNAs (miRNAs) are critical mediators of intercellular communication and play important roles in diverse physiological and pathological processes. However, existing EV miRNA databases are limited by outdated datasets, narrow sample diversity, and the absence of integrated analytical functions. Here, we present EVmiRNA2.0, a substantially updated database for miRNA expression in human EVs. EVmiRNA2.0 integrates 7254 human EV small RNA sequencing (smRNA-seq) samples from 45 distinct sources and 143 disease types. Compared with the previous version, EVmiRNA2.0 has the following key improvements: (i) a substantial increase in EVs datasets, expanding from 462 to 7254, a 15-fold augmentation in data volume; (ii) a flexible online differential expression analysis module, allowing users to filter and compare samples based on a project, EV subtype, sample source, and disease stage/treatment; (iii) an enhanced miRNA search system featuring cross-tissue, cross-fluid, and cross-cell-type expression profiles, along with curated functional annotation, predicted target genes, and drug interaction data; (iv) useful download options for both raw expression data and analysis results. With comprehensive datasets and improved functions, EVmiRNA2.0 will serve as a useful and indispensable resource for exploring the expression and function of EV-derived miRNAs. It is freely accessible at https://guolab.wchscu.cn/EVmiRNA2.0/.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-09-29
DOI
https://doi.org/10.1093/nar/gkaf1054
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
0.00

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article

EVmiRNA2.0: an updated database for miRNA expression in comprehensive human extracellular vesicles

Gui‐Yan Xie, An‐Yuan Guo, Qian Lei, Dandan Song et al.
Nucleic Acids Research
Extracellular vesicles in disease
article

EVmiRNA2.0: an updated database for miRNA expression in comprehensive human extracellular vesicles

Gui‐Yan Xie, An‐Yuan Guo, Qian Lei, Dandan Song, Tāo Luò
article en

Abstract

Extracellular vesicle (EV)-derived microRNAs (miRNAs) are critical mediators of intercellular communication and play important roles in diverse physiological and pathological processes. However, existing EV miRNA databases are limited by outdated datasets, narrow sample diversity, and the absence of integrated analytical functions. Here, we present EVmiRNA2.0, a substantially updated database for miRNA expression in human EVs. EVmiRNA2.0 integrates 7254 human EV small RNA sequencing (smRNA-seq) samples from 45 distinct sources and 143 disease types. Compared with the previous version, EVmiRNA2.0 has the following key improvements: (i) a substantial increase in EVs datasets, expanding from 462 to 7254, a 15-fold augmentation in data volume; (ii) a flexible online differential expression analysis module, allowing users to filter and compare samples based on a project, EV subtype, sample source, and disease stage/treatment; (iii) an enhanced miRNA search system featuring cross-tissue, cross-fluid, and cross-cell-type expression profiles, along with curated functional annotation, predicted target genes, and drug interaction data; (iv) useful download options for both raw expression data and analysis results. With comprehensive datasets and improved functions, EVmiRNA2.0 will serve as a useful and indispensable resource for exploring the expression and function of EV-derived miRNAs. It is freely accessible at https://guolab.wchscu.cn/EVmiRNA2.0/.

Nucleic Acids ResearchVol. 54(D1)
Wuhan University of Technology (CN), Sichuan University (CN), West China Medical Center of Sichuan University (CN), West China Hospital of Sichuan University (CN), Hubei University of Technology (CN), Hubei University (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Sichuan University, West China Hospital, Sichuan University
Openalex Percentile: Top 72%
Extracellular vesicles in disease
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