Evidence map›Paper›PMID 32269736›Full record

ArticleAmerican journal of translational research2020

Exosome-mediated miRNA delivery promotes liver cancer EMT and metastasis.

Qu Lin, Chu-Ren Zhou, Ming-Jun Bai, Duo Zhu, Jun-Wei Chen, Hao-Fan Wang, Ming-An Li, Chun Wu, Zheng-Ran Li, Ming-Sheng Huang

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 75 citations in OpenAlex.

  1. Review
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  3. EMT and cancer stem cells: Drivers of therapy resistance and promising therapeutic targets.Drug resistance updates : reviews and commentaries in antimicrobial and anticancer chemotherapy · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Qu LinDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Chu-Ren ZhouDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Ming-Jun BaiDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Duo ZhuDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Jun-Wei ChenDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Hao-Fan WangDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Ming-An LiDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Chun WuDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Zheng-Ran LiDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Ming-Sheng HuangDepartment of Interventional Radiology, The Third Affiliated Hospital of Sun Yat-Sen University Guangzhou 510630, China.
Sun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The deregulation of exosomal microRNAs (miRNAs) plays an important role in the progression of hepatocarcinogenesis. In this study, we highlight exosomes as mediators involved in modulating miRNA profiles in liver cancer cells after induction of the epithelial-mesenchymal transition (EMT) and metastasis. Initially, we induced EMT in a hepatocellular carcinoma cell (HCC) line (Hep3B) by stimulation with transforming growth factor-β (TGF-β) and confirmed by western blot detection of EMT markers such as vimentin and E-cadherin. Exosomes were then isolated from the cells and identified by nanoparticle tracking analysis (NTA). The isolated exosomal particles from unstimulated Hep3B cells (Hep3B exo) or TGF-β-stimulated EMT Hep3B cells (EMT-Hep3B exo) contained higher levels of exosome marker proteins, CD63 and TSG101. After incubation with EMT-Hep3B exo, Hep3B cell proliferation increased. EMT-Hep3B exo promoted the migration and invasion of Hep3B and 7721 cells. High-throughput sequencing of miRNAs and mRNA within the exosomes showed 119 upregulated and 186 downregulated miRNAs and 156 upregulated and 166 downregulated mRNA sequences in the EMT-Hep3B exo compared with the control Hep3B exo. The most differentially expressed miRNAs and target mRNA sequences were validated by RT-qPCR. Based on the known miRNA targets for specific mRNA sequences, we hypothesized that GADD45A was regulated by miR-374a-5p. Inhibition of miR-374a-5p in Hep3B cells resulted in exosomes that inhibited the proliferation, migration, and invasion of HCC cells. These results enhance our understanding of metastatic progression of liver cancer and provide a foundation for the future development of potential biomarkers for diagnosis and prognosis of hepatic cancer.

Indexed as

epithelial-mesenchymal transitionExosomeliver cancermetastasismicroRNATGF-β

Identifiers

PMID32269736
PMCPMC7137059
OpenAlexW3019635545

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.