Evidence map›Paper›PMID 23582036›Full record

ReviewCritical reviews in eukaryotic gene expression2013

Bi-directional signaling: extracellular matrix and integrin regulation of breast tumor progression.

Scott Gehler, Suzanne M Ponik, Kristin M Riching, Patricia J Keely

Open access · greenAbstract readReview
In one paragraph

Review in Critical reviews in eukaryotic gene expression, 2013. 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
3.1field-weighted citation impact, top 9% 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, 64 citations in OpenAlex.

  1. Review
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  9. Article
  10. Review
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  13. Chemotherapy treatment induces pro-invasive changes in liver ECM composition.Matrix biology : journal of the International Society for Matrix Biology · 2022
    Article
  14. Article
  15. Article
  16. Engineering complexity in human tissue models of cancer.Advanced drug delivery reviews · 2022
    Review
  17. Stiffness Sensing by Cells.Physiological reviews · 2020
    Review
  18. Article
  19. 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 3 institutions in 1 country.

Scott GehlerBiology Department, Augustana College, Rock Island, IL 61201, USA. scottgehler@augustana.edu
Suzanne M Ponik
Kristin M Riching
Patricia J Keely
Optica · USAugustana College · USUniversity of Wisconsin–Madison · US

Funding

Mechanisms Of Cell Migration On 3D Aligned MatricesR01CA142833 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI FRIEDL, ANDREAS, HAHN, KLAUS M. · 2010 to 2020
$3.4M
Biophysical Regulation of Breast DifferentiationR01CA114462 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI KEELY, PATRICIA J · 2010 to 2014
$1.5M
NCI NIH HHS CA114462-01A2NCI NIH HHS CA142833-01NCI NIH HHS R01 CA114462NCI NIH HHS R01 CA142833
6 · The paper itself

Abstract

Cell transformation and tumor progression involve a common set of acquired capabilities, including increased proliferation, failure of cell death, self-sufficiency in growth, angiogenesis, and tumor cell invasion and metastasis. The stromal environment consists of many cell types and various extracellular matrix (ECM) proteins that support normal tissue maintenance and which have been implicated in tumor progression. Both the chemical and mechanical properties of the ECM have been shown to influence normal and malignant cell behavior. For instance, mesenchymal stem cells differentiate into specific lineages that are dependent on matrix stiffness, while tumor cells undergo changes in cell behavior and gene expression in response to matrix stiffness. ECM remodeling is implicated in tumor progression and can result in increased deposition of stromal ECM, enhanced contraction of ECM fibrils, and altered collagen alignment and ECM stiffness. Tumor cells respond to changes in ECM remodeling through altered intracellular signaling and cell cycle control that lead to enhanced proliferation, loss of normal tissue architecture, and local tumor cell migration and invasion. This review focuses on the bi-directional interplay between the mechanical properties of the ECM and integrin-mediated signal transduction events in an effort to elucidate cell behaviors during tumor progression.

Indexed as

AnimalsBreast NeoplasmsCell CycleCell MovementCollagenDisease ProgressionExtracellular MatrixExtracellular Matrix ProteinsFemaleHumansIntegrinsMatrix Metalloproteinasesrho GTP-Binding ProteinsSignal TransductionCollagenExtracellular Matrix ProteinsIntegrinsMatrix Metalloproteinasesrho GTP-Binding Proteins

Identifiers

PMID23582036
PMCPMC5055378
OpenAlexW1976844904

What OpenQuestion holds

Textmetadata
LicenceTDM
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.