Evidence map›Paper›PMID 42834121›Full record

ReviewNature reviews. Genetics2026

Decoding epithelial-mesenchymal transitions with multi-omics.

Nitin Narwade, M Angela Nieto

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Nitin NarwadeInstituto de Neurociencias (CSIC-UMH), Sant Joan d'Alacant, Spain.
M Angela NietoInstituto de Neurociencias (CSIC-UMH), Sant Joan d'Alacant, Spain. anieto@umh.es.ORCID http://orcid.org/0000-0002-3538-840X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial-mesenchymal transition (EMT) is a highly dynamic and plastic cellular programme essential for embryonic development, tissue repair and ageing, and it is co-opted in pathological conditions such as cancer and fibrosis. The continuum of intermediate states and pronounced cellular heterogeneity that characterize EMT have historically limited systematic investigation across regulatory layers, including the transcriptome, epigenome, proteome and metabolome. Recent advances in high-throughput omics technologies, particularly single-cell and spatially resolved platforms, have enabled comprehensive profiling of cellular states at unprecedented resolution. These approaches, in parallel with computational methodologies such as machine learning frameworks, network-based modelling and integrative multi-omics, have been instrumental in extracting biological insight from intrinsically complex datasets. In this Review, we discuss how the convergence of emerging omics technologies and computational frameworks has advanced EMT research, outline key analytical considerations and discuss current challenges and future opportunities for biomarker discovery and translational applications.

Identifiers

PMID42834121

What OpenQuestion holds

Textmetadata
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.