Evidence map›Paper›PMID 33911465›Full record

ArticleWorld journal of gastroenterology2021

Lipotoxic hepatocyte-derived exosomal miR-1297 promotes hepatic stellate cell activation through the PTEN signaling pathway in metabolic-associated fatty liver disease.

Xin Luo, Sheng-Zheng Luo, Zi-Xin Xu, Cui Zhou, Zheng-Hong Li, Xiao-Yan Zhou, Ming-Yi Xu

Open access · hybridAbstract read
In one paragraph

Article in World journal of gastroenterology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 64 citations in OpenAlex.

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  13. Sinusoidal communication in chronic liver disease.Clinical and molecular hepatology · 2025
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  19. RNAkines are secreted messengers shaping health and disease.Trends in endocrinology and metabolism: TEM · 2024
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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 2 institutions in 1 country.

Xin LuoDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China.
Sheng-Zheng LuoDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China.
Zi-Xin XuDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China.
Cui ZhouDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China.
Zheng-Hong LiDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China.
Xiao-Yan ZhouDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China.
Ming-Yi XuDepartment of Gastroenterology, Shanghai General Hospital, Shanghai 200080, China. xumingyi2014@163.com.
SAIC-GM (China) · CNShanghai Stomatological Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExosomes play an important role in metabolic-associated fatty liver disease (MAFLD), but the mechanism by which exosomes participate in MAFLD still remain unclear.

aimTo figure out the function of lipotoxic exosomal miR-1297 in MAFLD.

methodsMicroRNA sequencing was used to detect differentially expressed miRNAs (DE-miR) in lipotoxic exosomes derived from primary hepatocytes. Bioinformatic tools were applied to analyze the target genes and pathways regulated by the DE-miRs. Quantitative real-time PCR (qPCR) was conducted for the verification of DE-miRs. qPCR, western blot, immunofluorescence staining and ethynyl-20-deoxyuridine assay were used to evaluate the function of lipotoxic exosomal miR-1297 on hepatic stellate cells (LX2 cells). A luciferase reporter experiment was performed to confirm the relationship of miR-1297 and its target gene

resultsMicroRNA sequencing revealed that there were 61 exosomal DE-miRs (

conclusionmiR-1297 was overexpressed in exosomes derived from lipotoxic hepatocytes. The lipotoxic hepatocyte-derived exosomal miR-1297 could promote the activation and proliferation of hepatic stellate cells through the PTEN/PI3K/AKT signaling pathway, accelerating the progression of MAFLD.

Indexed as

ExosomesMicroRNAsHepatic Stellate CellsHepatocytesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionMicroRNAsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktExosomeHepatic stellate cellLiver fibrosisMetabolic-associated fatty liver diseasemiRNA-1297PTEN

Identifiers

PMID33911465
PMCPMC8047533
OpenAlexW3153930089

What OpenQuestion holds

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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.