Evidence map›Paper›PMID 41233338›Full record

ArticleNPJ systems biology and applications2025

A computational approach for perturbation-induced EMT transitions.

Daniel Ramirez, David A Kessler, Mingyang Lu, Herbert Levine

Abstract read
In one paragraph

Article in NPJ systems biology and applications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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.

Daniel RamirezDepartment of Bioengineering, Northeastern University, Boston, MA, USA.
David A KesslerDepartment of Physics, Bar-Ilan University, Ramat-Gan, Israel.
Mingyang LuDepartment of Bioengineering, Northeastern University, Boston, MA, USA.
Herbert LevineDepartment of Bioengineering, Northeastern University, Boston, MA, USA. h.levine@northeastern.edu.

Funding

Center for Theoretical Biological Physics NSF PHY-2019745
6 · The paper itself

Abstract

The Epithelial-mesenchymal transition (EMT) is a cellular state transition fundamental to development, wound healing, and cancer metastasis. The gene regulatory mechanisms underlying EMT have been extensively documented, revealing gene regulatory networks (GRNs) involving groups of mutually inhibiting transcription factors and microRNAs. Despite significant progress from both experimental and computational approaches, the details of how the EMT GRN initiates EMT in response to various external inputs is still not well understood. Here, we apply both Boolean and ordinary differential equation (ODE)-based methods to simulate a well-studied 26-node, 100-edge EMT GRN, examining its response to a wide range of single- and double-node perturbations. We evaluate the characteristics of effective EMT-inducing signals, particularly examining the amplifying role of transcriptional noise in determining the likelihood and mean transit time of an EMT. Together, these models establish a complementary framework for understanding and predicting drivers of EMT in the context of a GRN. We anticipate that this framework for a systematic study of in-silico GRN perturbations will be useful in developing increasingly accurate dynamical GRN models for various biological processes.

Indexed as

Computational BiologyEpithelial-Mesenchymal TransitionAlgorithmsComputer SimulationGene Regulatory NetworksHumansTranscription FactorsTranscription Factors

Identifiers

PMID41233338
PMCPMC12615684

What OpenQuestion holds

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LicenceCC BY
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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.