Evidence map›Paper›PMID 31065520›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2019

Development of a Non-Coding-RNA-based EMT/CSC Inhibitory Nanomedicine for In Vivo Treatment and Monitoring of HCC.

Ruomi Guo, Zhiqiang Wu, Jing Wang, Qingling Li, Shunli Shen, Weiwei Wang, Luyao Zhou, Wei Wang, Zhong Cao, Yu Guo

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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  8. Tumour invasion and dissemination.Biochemical Society transactions · 2022
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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.

Ruomi GuoDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.ORCID https://orcid.org/0000-0002-8207-8746
Zhiqiang WuDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Jing WangDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Qingling LiDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Shunli ShenDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Weiwei WangDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Luyao ZhouDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Wei WangDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Zhong CaoDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.
Yu GuoDepartment of General Surgery The First Affiliated Hospital of Sun Yat-Sen University Guangzhou 510080 China.ORCID https://orcid.org/0000-0002-8886-0106

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study is to improve the overall prognosis of patients with hepatocellular carcinoma (HCC); therefore, new therapeutic methods that can be used in vivo are urgently needed. In this study, the relationship between the quantities of microRNA (miR)-125b-5p in clinical specimens and clinicopathological parameters is analyzed. A folate-conjugated nanocarrier is used to transfect miR-125b-5p in vivo and to observe the therapeutic effect on HCC. The inhibitory effect and mechanism of miR-125b-5p on hepatoma cells are also studied. Data from clinical specimens and in vitro experiments confirm that the miR-125b-5p quantity is negatively correlated with progression, and the target protein that regulates the epithelial-mesenchymal transition (EMT)/cancer stem cells (CSC) potential in HCC is STAT3. The miR-125b-5p/STAT3 axis inhibits the invasion, migration, and growth of HCC via inactivation of the wnt/β-Catenin pathway. miR-125b-5p-loaded nanomedicine effectively inhibits the EMT/CSC potential of hepatoma cells in vivo together with their magnetic resonance imaging (MRI) visualization characteristics. An HCC-therapeutic and MRI-visible nanomedicine platform that achieves noninvasive treatment effect monitoring and timely individualized treatment course adjustment is developed.

Indexed as

cancer stem cellsepithelial–mesenchymal transitionhepatocellular carcinomamicroRNA‐125b‐5pnanocarriers

Identifiers

PMID31065520
PMCPMC6498119

What OpenQuestion holds

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Registered trials

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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.