Evidence map›Paper›PMID 22203958›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2012

Mechanical compression drives cancer cells toward invasive phenotype.

Janet M Tse, Gang Cheng, James A Tyrrell, Sarah A Wilcox-Adelman, Yves Boucher, Rakesh K Jain, Lance L Munn

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 323 papers.

0numbers the graph read from it
0cells of the map it votes in
323citing 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

323 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. On why cancer cells require a great amount of glucose.Quantitative biology (Beijing, China) · 2026
    Article
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  13. Review
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  20. Review

263 more citing papers are in PubMed but not listed here.

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

7 authors.

Janet M TseDepartment of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Gang Cheng
James A Tyrrell
Sarah A Wilcox-Adelman
Yves Boucher
Rakesh K Jain
Lance L Munn

Funding

Vascular Normalization: Rolse of Perivascular CellsP01CA080124 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI JAIN, RAKESH K. · 2000 to 2016
$35.0M
CELL-SURFACE ADHESION--INFLUENCE OF BLOOD RHEOLOGYR01HL064240 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MUNN, LANCE L · 2000 to 2007
$2.2M
Blood rheology: analytical approaches to sickle cell diseaseR56HL064240 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MUNN, LANCE L. · 2009 to 2009
$443k
NCI NIH HHS P01 CA080124NCI NIH HHS P01CA080124NHLBI NIH HHS HL64240NHLBI NIH HHS R01 HL064240NHLBI NIH HHS R56 HL064240
6 · The paper itself

Abstract

Uncontrolled growth in a confined space generates mechanical compressive stress within tumors, but little is known about how such stress affects tumor cell behavior. Here we show that compressive stress stimulates migration of mammary carcinoma cells. The enhanced migration is accomplished by a subset of "leader cells" that extend filopodia at the leading edge of the cell sheet. Formation of these leader cells is dependent on cell microorganization and is enhanced by compressive stress. Accompanied by fibronectin deposition and stronger cell-matrix adhesion, the transition to leader-cell phenotype results in stabilization of persistent actomyosin-independent cell extensions and coordinated migration. Our results suggest that compressive stress accumulated during tumor growth can enable coordinated migration of cancer cells by stimulating formation of leader cells and enhancing cell-substrate adhesion. This novel mechanism represents a potential target for the prevention of cancer cell migration and invasion.

Indexed as

Stress, MechanicalActomyosinBreast NeoplasmsCell AdhesionCell Line, TumorCell-Matrix JunctionsCell MovementCytoskeletonFemaleHumansModels, BiologicalNeoplasm InvasivenessPhenotypePseudopodiaActomyosin

Identifiers

PMID22203958
PMCPMC3271885

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.