Evidence map›Paper›PMID 34511037›Full record

ArticleBioengineered2021

Long non-coding RNA AC012668 suppresses non-alcoholic fatty liver disease by competing for microRNA miR-380-5p with lipoprotein-related protein LRP2.

Xiaomeng Chen, Hong Ma, Yan Gao, Ye Jin, Wei Ning, Yue Hou, Jianrong Su

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.0field-weighted citation impact, top 27% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 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 2 institutions in 2 countries.

Xiaomeng ChenClinical Laboratory Center, Beijing Friendship Hospital, Capital Medical University, China.
Hong MaBeijing Friendship Hospital, Capital Medical University, Beijing, China.
Yan GaoClinical Laboratory Center, Beijing Friendship Hospital, Capital Medical University, China.
Ye JinClinical Laboratory Center, Beijing Friendship Hospital, Capital Medical University, China.
Wei NingClinical Laboratory Center, Beijing Friendship Hospital, Capital Medical University, China.
Yue HouClinical Laboratory Center, Beijing Friendship Hospital, Capital Medical University, China.
Jianrong SuClinical Laboratory Center, Beijing Friendship Hospital, Capital Medical University, China.
Capital Medical University · CNBeijing Friendship Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonalcoholic fatty liver disease (NAFLD) is characterized by high morbidity. Although long noncoding RNAs (lncRNAs) are known to have a role in NAFLD pathogenesis, the identified lncRNA types are limited. In this study, NAFLD models were established in vitro and in vivo using free fatty acid-treated LO2 cells and high-fat diet-fed mice, respectively. Microarray data were downloaded from the Gene Expression Omnibus database, and

Indexed as

Non-alcoholic Fatty Liver DiseaseAnimalsCell LineHumansLow Density Lipoprotein Receptor-Related Protein-2MaleMiceMice, Inbred C57BLMicroRNAsRNA, Long NoncodingLow Density Lipoprotein Receptor-Related Protein-2LRP2 protein, humanLrp2 protein, mouseMicroRNAsMIRN380 microRNA, humanMirn380 microRNA, mouseRNA, Long Noncodinghepatic steatosislong non-coding RNALRP2miR-380-5pNonalcoholic fatty liver disease

Identifiers

PMID34511037
PMCPMC8806601
OpenAlexW3200773505

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.