Evidence map›Paper›PMID 36864480›Full record

ArticleJournal of biological engineering2023

The ELF3 transcription factor is associated with an epithelial phenotype and represses epithelial-mesenchymal transition.

Ayalur Raghu Subbalakshmi, Sarthak Sahoo, Prakruthi Manjunatha, Shaurya Goyal, Vignesh A Kasiviswanathan, Yeshwanth Mahesh, Soundharya Ramu, Isabelle McMullen, Jason A Somarelli, Mohit Kumar Jolly

Open access · goldAbstract read
In one paragraph

Article in Journal of biological engineering, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
7.8field-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

28 citing papers in PubMed, 35 citations in OpenAlex.

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  14. Liver GPBAR1 Associates With Immune Dysfunction in Primary Sclerosing Cholangitis and Its Activation Attenuates Cholestasis in Abcb4-/- Mice.Liver international : official journal of the International Association for the Study of the Liver · 2025
    Article
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  16. Generation of Human 3D Airway Assembloids for Advanced Modeling.International journal of biological sciences · 2025
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  19. Epithelial-mesenchymal transition in tissue repair and degeneration.Nature reviews. Molecular cell biology · 2024
    Review
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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

10 authors at 6 institutions in 2 countries.

Ayalur Raghu SubbalakshmiCentre for BioSystems Science and Engineering, Indian Institute of Science, 560012, Bangalore, India.
Sarthak Sahoo *Centre for BioSystems Science and Engineering, Indian Institute of Science, 560012, Bangalore, India.
Prakruthi ManjunathaDepartment of Medical Electronics, M S Ramaiah Institute of Technology, 560054, Bangalore, India.
Shaurya GoyalDepartment of Humanities and Social Sciences, Indian Institute of Technology, 721302, Kharagpur, India.
Vignesh A KasiviswanathanDepartment of Biotechnology, JSS Science and Technology University, 570006, Mysore, India.
Yeshwanth MaheshCentre for BioSystems Science and Engineering, Indian Institute of Science, 560012, Bangalore, India.
Soundharya RamuDepartment of Biotechnology, National Institute of Technology Warangal, 506004, Warangal, India.
Isabelle McMullenDepartment of Medicine, Duke University, NC 27708, Durham, USA.
Jason A SomarelliDepartment of Medicine, Duke University, NC 27708, Durham, USA. jason.somarelli@duke.edu.
Mohit Kumar JollyCentre for BioSystems Science and Engineering, Indian Institute of Science, 560012, Bangalore, India. mkjolly@iisc.ac.in.
Indian Institute of Science Bangalore · INDuke University · USIndian Institute of Technology Kharagpur · INJSS Science and Technology University · INM.S. Ramaiah Medical College · INNational Institute of Technology Warangal · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEpithelial-mesenchymal plasticity (EMP) involves bidirectional transitions between epithelial, mesenchymal and multiple intermediary hybrid epithelial/mesenchymal phenotypes. While the process of epithelial-mesenchymal transition (EMT) and its associated transcription factors are well-characterised, the transcription factors that promote mesenchymal-epithelial transition (MET) and stabilise hybrid E/M phenotypes are less well understood.

resultsHere, we analyse multiple publicly-available transcriptomic datasets at bulk and single-cell level and pinpoint ELF3 as a factor that is strongly associated with an epithelial phenotype and is inhibited during EMT. Using mechanism-based mathematical modelling, we also show that ELF3 inhibits the progression of EMT. This behaviour was also observed in the presence of an EMT inducing factor WT1. Our model predicts that the MET induction capacity of ELF3 is stronger than that of KLF4, but weaker than that of GRHL2. Finally, we show that ELF3 levels correlates with worse patient survival in a subset of solid tumour types.

conclusionELF3 is shown to be inhibited during EMT progression and is also found to inhibit the progression of complete EMT suggesting that ELF3 may be able to counteract EMT induction, including in the presence of EMT-inducing factors, such as WT1. The analysis of patient survival data indicates that the prognostic capacity of ELF3 is specific to cell-of-origin or lineage.

Indexed as

ELF3Epithelial-mesenchymal transition (EMT)Epithelial Transition (MET)Mathematical modellingMesenchymalPhenotypic plasticity

Identifiers

PMID36864480
PMCPMC9983220
OpenAlexW4322766974

What Socratic holds

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LicenceCC BY
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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 Socratic graph.