Evidence map›Paper›PMID 35005119›Full record

ArticleGenes & diseases2022

Comparison of hepatic gene expression profiles between three mouse models of Nonalcoholic Fatty Liver Disease.

Liping Xiang, Yang Jiao, Yiling Qian, Yao Li, Fei Mao, Yan Lu

Open access · diamondAbstract read
In one paragraph

Article in Genes & diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.2field-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

15 citing papers in PubMed, 24 citations in OpenAlex.

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  12. The Effects of ProbioticInternational journal of molecular sciences · 2023
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  15. A Transcriptomic Response toInternational journal of molecular sciences · 2022
    Article
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

6 authors at 2 institutions in 1 country.

Liping XiangDepartment of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Yang JiaoDepartment of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Yiling QianDepartment of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Yao LiDepartment of Laboratory Animal Science, Shanghai Jiao Tong University School of Medicine, Shanghai 200025, PR China.
Fei MaoDepartment of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Yan LuDepartment of Endocrinology and Metabolism, Zhongshan Hospital, Fudan University, Shanghai 200032, PR China.
Sun Yat-sen University · CNShanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-alcoholic fatty liver disease (NAFLD) has become the most common chronic liver disorder worldwide. Murine models of NAFLD have been widely used to explore its pathogenesis. In this study, we performed a systematic evaluation of hepatic genome-wide mRNA expression by RNA-Sequencing using three mouse models of NAFLD: leptin receptor deficient db/db mice, high-fat high-sugar diet (HSHF)-induced obese mice, and dexamethasone (DEX)-induced NAFLD mice. As a result, we found both distinct and common pathways in the regulation of lipid metabolism from transcriptomes of three mouse models. Moreover, only a total of 12 differentially expressed genes (DEGs) were commonly detected among all three mouse groups, indicating very little overlap among all three models. Therefore, our results suggest that NAFLD is a heterogeneous disease with highly variable molecular mechanisms.

Indexed as

DEGsMurine modelsNAFLDPathway analysisTranscriptome

Identifiers

PMID35005119
PMCPMC8720708
OpenAlexW3135260963

What OpenQuestion holds

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Registered trials

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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.