Evidence map›Paper›PMID 33037981›Full record

ArticleHepatology international2020

Exosomal miR-199a-5p promotes hepatic lipid accumulation by modulating MST1 expression and fatty acid metabolism.

Yuhan Li, Yansong Luan, Jianning Li, Hui Song, Yan Li, Hi Qi, Bo Sun, Peng Zhang, Xianxian Wu, Xing Liu and 5 more

Abstract read
PubMed Publisher
In one paragraph

Article in Hepatology international, 2020. 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
2.7field-weighted citation impact, top 8% 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, 61 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

15 authors at 4 institutions in 2 countries.

Yuhan LiSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Yansong LuanSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Jianning LiSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Hui SongSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Yan LiSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Hi QiSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Bo SunSecond Affiliated Hospital, Ningxia Medical University, Yinchuan, China.
Peng ZhangSecond Affiliated Hospital, Ningxia Medical University, Yinchuan, China.
Xianxian WuInstitute of Laboratory Animal Science (ILAS), Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS&PUMC), #5 Pan Jia Yuan Nan Li, Chaoyang Districe, Beijing, 100021, China.
Xing LiuInstitute of Laboratory Animal Science (ILAS), Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS&PUMC), #5 Pan Jia Yuan Nan Li, Chaoyang Districe, Beijing, 100021, China.
Yanhui YangSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China.
Wufan TaoInstitute of Developmental Biology and Molecular Medicine and State Key Laboratory of Genetic Engineering, School of Life Sciences, Fudan University, Shanghai, China.
Lei CaiDepartment of Physiology, Cardiovascular Research Center, University of Kentucky, Lexington, KY, 40536, USA.
Zhiwei YangInstitute of Laboratory Animal Science (ILAS), Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS&PUMC), #5 Pan Jia Yuan Nan Li, Chaoyang Districe, Beijing, 100021, China. yangzhiwei@cnilas.pumc.edu.cn.
Yi YangSchool of Basic Medical Sciences, Ningxia Medical University, Xingqing District, 692 Shengli St, Yinchuan, 75004, China. yangyi0908666@163.com.ORCID http://orcid.org/0000-0002-0062-7781
Ningxia Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CNFudan University · CNUniversity of Kentucky · US

Funding

Chinese Ministry of Education Z2016039National Natural Science Foundation of China 81670798 and 81460166National Natural Science Foundation of China 81800402
6 · The paper itself

Abstract

BACKGROUND AND

aimsNon-alcoholic fatty liver disease (NAFLD) and its complications has become an expanding health problem worldwide with limited therapeutic approaches. The current study was aiming to identify novel microRNA in the regulation of hepatic lipid metabolism in NAFLD. APPROCHES AND

resultsSystematic screening of microRNA expression by high-throughput small RNA sequencing demonstrated that microRNA 199a-5p (miR-199a-5p) was significantly upregulated in high fat diet-induced steatosis mouse model, with the most abundant expression in adipose tissue. MST1 was further identified as the target gene for miR-199a with specific recognition at the 3' untranslated region with dural luciferase reporter assay. Delivery of miR-199a-5p with exosomes into mice aggravated liver lipid accumulation in hepatocytes, accompanied by down-regulation of hepatic MST1 expression and modulation of hepatic lipogenesis and lipolysis, including SREBP-1c, AMPK signaling cascades and the down-stream CPT1α and FASN. Conversely, administration of exosome containing anti-miR-199a-5p resulted in attenuated steotosis in mice fed on high fat diet. Importanly, miR-199a-5p-induced abnormal cellular lipid accumulation could be markedly reversed by overexpression of MST1.

conclusionmiR-199a-5p might be an essentail regulator for hepatic lipid metabolism, possibly through its interction with MST1 and the subsequent signaling cascade. Thus, miR-199a-5p may serve as an important therapeutic target in the treatment of NAFLD.

Indexed as

MicroRNAsNon-alcoholic Fatty Liver DiseaseAnimalsFatty AcidsHepatocyte Growth FactorLipid MetabolismMiceProto-Oncogene ProteinsFatty AcidsHepatocyte Growth Factormacrophage stimulating proteinMicroRNAsMirn199 microRNA, mouseProto-Oncogene ProteinsExosomesmiR-199a-5pMST1NAFLD

Identifiers

PMID33037981
OpenAlexW3092226665

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.