Evidence map›Paper›PMID 34431063›Full record

ArticleHuman cell2021

Mesenchymal stem cell-derived exosomes block malignant behaviors of hepatocellular carcinoma stem cells through a lncRNA C5orf66-AS1/microRNA-127-3p/DUSP1/ERK axis.

Hao Gu, Chao Yan, Haijun Wan, Lin Wu, Junjie Liu, Zhiqiang Zhu, Dazhi Gao

Abstract read
PubMed Publisher
In one paragraph

Article in Human cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 53 citations in OpenAlex.

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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

7 authors at 4 institutions in 1 country.

Hao Gu *Department of Liver·Laparoscopic Surgery, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830054, Xinjiang, People's Republic of China.
Chao Yan *Department of Radiation Oncology, Qilu Hospital (Qingdao), Cheeloo College of Medicine, Shandong University, Qingdao, 266035, Shandong, People's Republic of China.
Haijun WanDepartment of Gastroenterology and Hepatology, Jinling Hospital Affiliated to Nanjing University School of Medicine, No. 305, East Zhongshan Road, Nanjing, 210002, Jiangsu, People's Republic of China. Wanhj11241@126.com.ORCID http://orcid.org/0000-0001-6739-6749
Lin WuDepartment of Gastroenterology and Hepatology, Jinling Hospital Affiliated to Nanjing University School of Medicine, No. 305, East Zhongshan Road, Nanjing, 210002, Jiangsu, People's Republic of China.
Junjie LiuDepartment of Liver·Laparoscopic Surgery, The First Affiliated Hospital of Xinjiang Medical University, Urumqi, 830054, Xinjiang, People's Republic of China.
Zhiqiang ZhuDepartment of Anorectal Surgery, Yantai Affiliated Hospital, Binzhou Medical College, Yantai, 264117, Shandong, People's Republic of China.
Dazhi GaoDepartment of Radiology Intervention, Jinling Hospital Affiliated to Nanjing University School of Medicine, No. 305, East Zhongshan Road, Nanjing, 210002, Jiangsu, People's Republic of China.
Nanjing General Hospital of Nanjing Military Command · CNXinjiang Medical University · CNBinzhou Medical University · CNShandong University · CN

Funding

Natural Science Foundation of Xinjiang Uygur Autonomous Region 2017D01C306
6 · The paper itself

Abstract

Mesenchymal stem cell (MSCs)-derived exosomes have been frequently used as useful tools in disease control. This research aimed to study the function of MSC-derived exosomes (Exo) in the stemness of cancer stem cells (CSCs) of hepatocellular carcinoma (HCC) and the molecular mechanism. Exo from the procured human bone marrow-MSCs were extracted and identified. CSCs from HCC cell lines were collected. The CSCs were treated with Exo, and then the proliferation, migration, invasion, angiogenesis-stimulating and self-renewal abilities of the Hep3B-CSCs and HuH7-CSCs were significantly reduced. C5orf66-AS1 was found as the most upregulated long noncoding RNAs (lncRNAs) in CSCs after Exo treatment. The integrated bioinformatic analyses and luciferase assays suggested that C5orf66-AS1 upregulated DUSP1 expression through sequestering microRNA-127-3p (miR-127-3p). Either artificial overexpression of miR-127-3p or silencing of DUSP1 blocked the inhibitory functions of Exo in the CSCs. DUSP1 inhibition increased the phosphorylation of ERK. Similar results were reproduced in vivo where Exo reduced the growth of xenograft formed by CSCs in nude mice, and this reduction was blocked upon miR-127-3p overexpression or DUSP1 silencing. To conclude, this research reported that MSC-derived Exo block malignant behaviors of HCC-sourced CSCs through a C5orf66-AS1/miR-127-3p/DUSP1/ERK axis.

Indexed as

AnimalsCarcinoma, HepatocellularCell Line, TumorCell MovementCell ProliferationCell Self RenewalDual Specificity Phosphatase 1ExosomesExtracellular Signal-Regulated MAP KinasesGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsLiver NeoplasmsMesenchymal Stem CellsMiceMice, NudeDual Specificity Phosphatase 1DUSP1 protein, humanExtracellular Signal-Regulated MAP KinasesMicroRNAsMIRN127 microRNA, humanRNA, Long NoncodingC5orf66-AS1Cancer stem cellsDUSP1ExosomesHepatocellular carcinomaMesenchymal stem cellsMicroRNA-127-3p

Identifiers

PMID34431063
OpenAlexW3194386192

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.