Evidence map›Paper›PMID 39930447›Full record

ArticleJournal of ovarian research2025

Dynamic and functional analyses of exosomal miRNAs regulating cellular microenvironment of ovarian cancer cells.

Zhaoxia Wang, Yanan Huang, Simin He, Ying Zhou, Le Zhao, Fuyuan Wang

Abstract read
In one paragraph

Article in Journal of ovarian research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Zhaoxia WangDepartment of Gynecology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China. wzx35181196@126.com.
Yanan HuangDepartment of Gynecology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Simin HeDepartment of Health Statistics and Epidemiology, School of Public Health, Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Ying ZhouDepartment of Gynecology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Le ZhaoDepartment of Gynecology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.
Fuyuan WangDepartment of Gynecology, First Hospital of Shanxi Medical University, Taiyuan, Shanxi, People's Republic of China.

Funding

The Key Medical Research Projects of Shanxi Province 2021XM36
6 · The paper itself

Abstract

backgroundExosomes, extracellular vesicles with an average diameter of 30 ~ 150 nm, are pivotal in mediating the cellular microenvironment (CM) through their cargo-carrying capability. Despite extensive studies, the dynamic and regulatory mechanisms of exosomal cargoes, including lipids, proteins, nucleic acids, and metabolites, remain poorly understood.

methodsIn this study, we collected culture medium of ovarian cancer cells at four different time points (12, 24, 36, 48 h). Exosomes were isolated using ultracentrifugation, and miRNA sequencing was performed for exosomes from each group (T12, T24, T36, and T48).

resultsA total of 131 miRNAs were identified in all groups. Specifically, 41, 115, 63, and 24 miRNAs were detected in the T12, T24, T36, and T48 groups, respectively. Among these, 15 miRNAs were common to the all groups, while 3, 57, 10, and 3 miRNAs were unique to the T12, T24, T36, and T48 groups, respectively. Functional analyses of the target genes for both common and specific miRNAs indicated that numerous target genes were involved in signaling pathways and cancer-related processes.

conclusionIt suggested that exosomal miRNAs might be critical in intercellular communication and in dynamically remodeling the tumor microenvironment. These insights could enhance our understanding of the role of exosomal miRNAs in cancer biology and inform the development of novel therapeutic strategies.

Indexed as

ExosomesMicroRNAsOvarian NeoplasmsTumor MicroenvironmentCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansMicroRNAsCellular microenvironmentExsomesmiRNAsmiRNA sequencingOvarian cancer

Identifiers

PMID39930447
PMCPMC11808964

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.