Evidence map›Paper›PMID 31656200›Full record

ArticleMolecular cancer2019

Exosomal miR-21 regulates the TETs/PTENp1/PTEN pathway to promote hepatocellular carcinoma growth.

Liang-Qi Cao, Xue-Wei Yang, Yu-Bin Chen, Da-Wei Zhang, Xiao-Feng Jiang, Ping Xue

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 119 papers.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed
8.9field-weighted citation impact, top 1% 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

119 citing papers in PubMed, 176 citations in OpenAlex.

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  8. The Role of miRNA-21 in the Metastasis of Hepatocellular Carcinoma as a Therapeutic Target.International journal of hematology-oncology and stem cell research · 2026
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  16. Dysregulated miRNAs Targeting Adiponectin Signaling in Colorectal Cancer.International journal of molecular sciences · 2025
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59 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Liang-Qi CaoDepartment of Hepatobiliary Surgery, the Second Affiliated Hospital of Guangzhou Medical University, 250# Changgang East Road, Haizhu District, Guangzhou, 510260, People's Republic of China. clq0829@163.com.ORCID http://orcid.org/0000-0001-9111-0456
Xue-Wei YangDepartment of Hepatobiliary Surgery, the Second Affiliated Hospital of Guangzhou Medical University, 250# Changgang East Road, Haizhu District, Guangzhou, 510260, People's Republic of China.
Yu-Bin ChenDepartment of Hepatobiliary Surgery, the Second Affiliated Hospital of Guangzhou Medical University, 250# Changgang East Road, Haizhu District, Guangzhou, 510260, People's Republic of China.
Da-Wei ZhangDepartment of Hepatobiliary Surgery, the Second Affiliated Hospital of Guangzhou Medical University, 250# Changgang East Road, Haizhu District, Guangzhou, 510260, People's Republic of China.
Xiao-Feng JiangDepartment of Hepatobiliary Surgery, the Second Affiliated Hospital of Guangzhou Medical University, 250# Changgang East Road, Haizhu District, Guangzhou, 510260, People's Republic of China.
Ping XueDepartment of Hepatobiliary Surgery, the Second Affiliated Hospital of Guangzhou Medical University, 250# Changgang East Road, Haizhu District, Guangzhou, 510260, People's Republic of China.
Second Affiliated Hospital of Guangzhou Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs an important means of communication, exosomes play an important role in the development of hepatocellular carcinoma (HCC).

methodsBioinformatics analysis, dual-luciferase reporter assays, methylation-specific quantitative PCR, and ChIP-PCR analysis were used to gain insight into the underlying mechanism of miR-21 in HCC.

resultsThe detection of miRNAs in exosomes of HCC showed that miR-21 expression in exosomes was positively correlated with the expression level of miR-21 in cells and negatively correlated with the expression of its target genes PTEN, PTENp1 and TETs. HCC cell-derived exosomes could increase miR-21 and p-Akt expression in HCC cells and downregulate the expression of PTEN, PTENp1 and TETs. MiR-21 inhibitors or PTENp1 overexpression vectors could weaken the effect of the abovementioned exosomes and simultaneously weaken their role in promoting cell proliferation and migration and inhibiting apoptosis. Further studies showed that miR-21 not only directly regulated the expression of PTEN, PTENp1 and TETs but also increased the methylation level of the PTENp1 promoter by regulating the expression of TETs, thereby inhibiting the expression of PTENp1 and further downregulating the expression of PTEN.

conclusionsExosomal miR-21 can regulate the expression of the tumor suppressor genes PTEN and PTENp1 in various ways and affect the growth of HCC cells.

Indexed as

ExosomeHepatocellular carcinomamiR-21PTENPTENp1TET

Identifiers

PMID31656200
PMCPMC6815431
OpenAlexW2981871574

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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.