Evidence map›Paper›PMID 33345692›Full record

ArticleAdipocyte2021

Mouse Embryonic Fibroblast Adipogenic Potential: A Comprehensive Transcriptome Analysis.

Mohamed Al-Sayegh, Hamad Ali, Mohammad H Jamal, Mei ElGindi, Tina Chanyong, Khulood Al-Awadi, Mohamed Abu-Farha

Open access · goldAbstract read
In one paragraph

Article in Adipocyte, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
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  10. The Use of Stem Cell-Derived Organoids in Disease Modeling: An Update.International journal of molecular sciences · 2021
    Review
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 3 institutions in 2 countries.

Mohamed Al-SayeghNew York University Abu Dhabi , Division of Biology, Abu Dhabi, United Arab Emirates.ORCID 0000-0003-3865-1688
Hamad AliDepartment of Medical Laboratory Sciences, Faculty of Allied Health Sciences, Health Sciences Center (HSC), Kuwait University , Kuwait City, State of Kuwait.ORCID 0000-0001-6623-3374
Mohammad H JamalDepartment of Surgery, Faculty of Medicine, Health Sciences Center (HSC), Kuwait University , Kuwait City, State of Kuwait.
Mei ElGindiNew York University Abu Dhabi , Division of Biology, Abu Dhabi, United Arab Emirates.
Tina ChanyongNew York University Abu Dhabi , Division of Biology, Abu Dhabi, United Arab Emirates.
Khulood Al-AwadiNew York University Abu Dhabi, Design Studio , Abu Dhabi, United Arab Emirates.
Mohamed Abu-FarhaDepartment of Biochemistry and Molecular Biology, Dasman Diabetes Institute (DDI) , Kuwait City, State of Kuwait.ORCID 0000-0001-8357-1252
New York University Abu Dhabi · AEKuwait University · KWDasman Diabetes Institute · KW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our understanding of adipose tissue has progressed from an inert tissue for energy storage to be one of the largest endocrine organs regulating metabolic homoeostasis through its ability to synthesize and release various adipokines that regulate a myriad of pathways. The field of adipose tissue biology is growing due to this association with various chronic metabolic diseases. An important process in the regulation of adipose tissue biology is adipogenesis, which is the formation of new adipocytes. Investigating adipogenesis in vitro is currently a focus for identifying factors that might be utilized in clinically. A powerful tool for such work is high-throughput sequencing which can rapidly identify changes at gene expression level. Various cell models exist for studying adipogenesis and has been used in high-throughput studies, yet little is known about transcriptome profile that underlies adipogenesis in mouse embryonic fibroblasts. This study utilizes RNA-sequencing and computational analysis with DESeq2, gene ontology, protein-protein networks, and robust rank analysis to understand adipogenesis in mouse embryonic fibroblasts in-depth. Our analyses confirmed the requirement of mitotic clonal expansion prior to adipogenesis in this cell model and highlight the role of

Indexed as

3T3-L1 CellsAdipocytesAdipogenesisAdipokinesAdipose TissueAnimalsCell DifferentiationFibroblastsGene ExpressionGene Expression ProfilingGene Expression RegulationHigh-Throughput Nucleotide SequencingMiceMouse Embryonic Stem CellsSequence Analysis, RNATranscriptomeAdipokinesadipocyte differentiationadipogenesisAdipose tissuemouse embryonic fibroblasttranscriptome

Identifiers

PMID33345692
PMCPMC7757854
OpenAlexW3116040510

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.