Evidence map›Paper›PMID 32416243›Full record

ReviewMatrix biology : journal of the International Society for Matrix Biology2020

Spatial-omics: Novel approaches to probe cell heterogeneity and extracellular matrix biology.

Grace C Bingham, Fred Lee, Alexandra Naba, Thomas H Barker

Abstract readReview
In one paragraph

Review in Matrix biology : journal of the International Society for Matrix Biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing 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

54 citing papers in PubMed.

  1. Article
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  5. Untangling the fusion of spatial omics and mechanobiology.Progress in biomedical engineering (Bristol, England) · 2025
    Review
  6. Article
  7. Article
  8. Article
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  10. Article
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  19. Local, Quantitative Morphometry of Fibroproliferative Lung Injury Using Laminin.American journal of respiratory cell and molecular biology · 2024
    Article
  20. 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

4 authors.

Grace C BinghamDepartment of Biomedical Engineering, 415 Lane Road, University of Virginia, Charlottesville, VA 22903, USA.
Fred LeeDepartment of Physiology and Biophysics, University of Illinois at Chicago, 835 S. Wolcott Ave, Chicago, IL 60612, USA.
Alexandra NabaDepartment of Physiology and Biophysics, University of Illinois at Chicago, 835 S. Wolcott Ave, Chicago, IL 60612, USA; University of Illinois at Chicago Cancer Center, Chicago, 835 S. Wolcott Ave, Chicago, IL 60612, USA.
Thomas H BarkerDepartment of Biomedical Engineering, 415 Lane Road, University of Virginia, Charlottesville, VA 22903, USA. Electronic address: thomas.barker@virginia.edu.

Funding

Cancer Research Training Program: From Molecular Mechanisms to Therapeutic StrategiesT32CA009109 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI Andrew Carl Dudley, Melanie R Rutkowski · 1985 to 2026
$13.9M
Mechanosensors that detect and treat Lung FibrosisR01HL132585 · NHLBI · UNIVERSITY OF VIRGINIA · PI BARKER, THOMAS HARRISON · 2015 to 2019
$3.3M
Targeting the alpha v integrin mechanotransduction axis in IPFR01HL127283 · NHLBI · UNIVERSITY OF VIRGINIA · PI BARKER, THOMAS HARRISON · 2015 to 2018
$1.6M
2019 American Society for Matrix Biology Workshop on Fibroblasts: The Arbiters of Matrix RemodelingR13HL149435 · NHLBI · UNIVERSITY OF VIRGINIA · PI BARKER, THOMAS HARRISON · 2019 to 2019
$8k
NCI NIH HHS T32 CA009109NHLBI NIH HHS R01 HL127283NHLBI NIH HHS R01 HL132585NHLBI NIH HHS R13 HL149435
6 · The paper itself

Abstract

Complex intercellular interactions as well as biomolecular and biomechanical cues from the extracellular matrix (ECM) profoundly affect cellular functions. Traditional transcriptomic and proteomic approaches have provided insight into disease progression by identifying discrete cellular subpopulations or microenvironmental signatures characteristic of normal or pathological tissues, however these techniques do not examine how a given cellular state relates to its interactions with neighboring cells or its surrounding ECM with multiparametric characterization (i.e. ECM alignment, mechanical forces, crosslinking, etc.). Emerging spatial-omic techniques can provide high-resolution mapping of expression profiles similar to scRNA-seq and mass spectroscopy directly within tissues. The ability to preserve the spatial context of cells within samples, their cellular geometry, as well as their surrounding ECM gives spatial-omics the opportunity to interrogate previously unexplored signaling modalities, which has the potential to revolutionize ECM research and our understanding of fibrotic diseases. In this review, we present current spatial transcriptomic and proteomic techniques and discuss how they may be applied to investigate cell-ECM interactions.

Indexed as

TranscriptomeAnimalsBiomechanical PhenomenaCell LineageExtracellular MatrixExtracellular Matrix ProteinsFibroblastsFibrosisFluorescent DyesGene Expression RegulationHigh-Throughput Nucleotide SequencingHumansIn Situ Hybridization, FluorescenceMolecular ImagingProteomicsRNA, MessengerExtracellular Matrix ProteinsFluorescent DyesRNA, Messengerfibrosismatrisomemultiplex imagingspatial proteomicsSpatial transcriptomics

Identifiers

PMID32416243
PMCPMC9278047

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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 OpenQuestion graph.