Evidence map›Paper›PMID 32870263›Full record

ArticleNucleic acids research2020

Inference and multiscale model of epithelial-to-mesenchymal transition via single-cell transcriptomic data.

Yutong Sha, Shuxiong Wang, Peijie Zhou, Qing Nie

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

39 citing papers in PubMed, 70 citations in OpenAlex.

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  5. Engineering CAR-T Therapeutics for Enhanced Solid Tumor Targeting.Advanced materials (Deerfield Beach, Fla.) · 2025
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  11. Single-Cell Informatics for Tumor Microenvironment and Immunotherapy.International journal of molecular sciences · 2024
    Review
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  15. Article
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  17. Article
  18. Application of single-cell RNA sequencing in head and neck squamous cell carcinoma.Chinese journal of cancer research = Chung-kuo yen cheng yen chiu · 2023
    Article
  19. Single-cell CaJournal of the Royal Society, Interface · 2023
    Article
  20. 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

4 authors at 1 institution in 1 country.

Yutong ShaDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.
Shuxiong WangDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.
Peijie ZhouDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.
Qing NieDepartment of Mathematics, University of California, Irvine, Irvine, CA 92697, USA.
University of California, Irvine · US

Funding

Shared Resource Core: Single Cell AnalysisU54CA217378 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI LANDER, ARTHUR D · 2018 to 2022
$9.7M
Transcriptional Co-Regulators in EpidermisR01AR044882 · NIAMS · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI Bogi Andersen · 1998 to 2026
$9.0M
Multiscale Models of Wound Cell Plasticity for RegenerationU01AR073159 · NIAMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI DAI, XING, NIE, QING · 2018 to 2022
$3.5M
National Science Foundation DMS1763272NCI NIH HHS U54 CA217378NIAMS NIH HHS R01 AR044882NIAMS NIH HHS U01 AR073159
6 · The paper itself

Abstract

Rapid growth of single-cell transcriptomic data provides unprecedented opportunities for close scrutinizing of dynamical cellular processes. Through investigating epithelial-to-mesenchymal transition (EMT), we develop an integrative tool that combines unsupervised learning of single-cell transcriptomic data and multiscale mathematical modeling to analyze transitions during cell fate decision. Our approach allows identification of individual cells making transition between all cell states, and inference of genes that drive transitions. Multiscale extractions of single-cell scale outputs naturally reveal intermediate cell states (ICS) and ICS-regulated transition trajectories, producing emergent population-scale models to be explored for design principles. Testing on the newly designed single-cell gene regulatory network model and applying to twelve published single-cell EMT datasets in cancer and embryogenesis, we uncover the roles of ICS on adaptation, noise attenuation, and transition efficiency in EMT, and reveal their trade-off relations. Overall, our unsupervised learning method is applicable to general single-cell transcriptomic datasets, and our integrative approach at single-cell resolution may be adopted for other cell fate transition systems beyond EMT.

Indexed as

Gene Expression ProfilingGene Regulatory NetworksModels, BiologicalAnimalsCell DifferentiationEmbryonic Stem CellsEpithelial-Mesenchymal TransitionGene Expression Regulation, NeoplasticHead and Neck NeoplasmsHumansMiceSingle-Cell AnalysisSkin NeoplasmsSquamous Cell Carcinoma of Head and Neck

Identifiers

PMID32870263
PMCPMC7515733
OpenAlexW3081981716

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.