Evidence map›Paper›PMID 37957268›Full record

ArticleNature materials2024

Cell volume expansion and local contractility drive collective invasion of the basement membrane in breast cancer.

Julie Chang, Aashrith Saraswathibhatla, Zhaoqiang Song, Sushama Varma, Colline Sanchez, Naomi Hassan Kahtan Alyafei, Dhiraj Indana, Raleigh Slyman, Sucheta Srivastava, Katherine Liu and 6 more

Open access · greenAbstract read
In one paragraph

Article in Nature materials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
12.3field-weighted citation impact, top 1% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  7. Review
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  11. Integrin-Piezo1 Axis Drives ECM Remodeling and Invasion of 3D Breast Epithelium.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  12. Extracellular Matrix Viscoelasticity Regulates Mammary Branching Morphogenesis.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Collective migration modes in development, tissue repair and cancer.Nature reviews. Molecular cell biology · 2025
    Review
  18. Article
  19. Article
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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

16 authors at 5 institutions in 1 country.

Julie Chang *Department of Bioengineering, Stanford University, Stanford, CA, USA.ORCID 0000-0002-8433-5902
Aashrith Saraswathibhatla *Department of Mechanical Engineering, Stanford University, Stanford, CA, USA.ORCID 0000-0002-0971-8065
Zhaoqiang SongCenter for Engineering Mechanobiology, University of Pennsylvania, Philadelphia, PA, USA.
Sushama VarmaDepartment of Pathology, Stanford University Medical Center, Palo Alto, CA, USA.
Colline SanchezDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, USA.
Naomi Hassan Kahtan AlyafeiDepartment of Bioengineering, Stanford University, Stanford, CA, USA.
Dhiraj IndanaDepartment of Mechanical Engineering, Stanford University, Stanford, CA, USA.ORCID 0000-0002-8644-5048
Raleigh SlymanDepartment of Mechanical Engineering, Stanford University, Stanford, CA, USA.
Sucheta SrivastavaDepartment of Pathology, Stanford University Medical Center, Palo Alto, CA, USA.
Katherine LiuDepartment of Genetics, Stanford University Medical Center, Palo Alto, CA, USA.
Michael C BassikDepartment of Genetics, Stanford University Medical Center, Palo Alto, CA, USA.
M Peter MarinkovichDepartment of Dermatology, Stanford University School of Medicine, Stanford, CA, USA.
Louis HodgsonDepartment of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, USA.ORCID 0000-0001-9188-7580
Vivek ShenoyCenter for Engineering Mechanobiology, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-2645-1016
Robert B WestDepartment of Pathology, Stanford University Medical Center, Palo Alto, CA, USA.
Ovijit ChaudhuriDepartment of Mechanical Engineering, Stanford University, Stanford, CA, USA. chaudhuri@stanford.edu.ORCID 0000-0002-9287-3401
Stanford University · USStanford Medicine · USAlbert Einstein College of Medicine · USUniversity of Pennsylvania · USVeterans Health Administration · US

Funding

Studying E-cadherin dynamics during extravasation and metastatic colonizationU54CA261694 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI ROGER D KAMM · 2021 to 2026
$9.1M
Pathological consequences of altered tissue mechanics in fibrosisR01EB017753 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI JANMEY, PAUL A, SHENOY, VIVEK · 2014 to 2025
$6.3M
Multiplex Imaging of Signaling Pathways in Cell MotilityR35GM136226 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Louis Hodgson · 2020 to 2026
$5.3M
Role of extracellular matrix malleability in mediating breast cancer cell invasion and migrationR37CA214136 · NCI · STANFORD UNIVERSITY · PI CHAUDHURI, OVIJIT · 2018 to 2024
$2.5M
Integration of elasticity, viscosity, and plasticity in cellular mechanosensingR01EB030876 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI SHENOY, VIVEK · 2020 to 2023
$1.3M
NCI NIH HHS R37 CA214136NCI NIH HHS U54 CA261694NIBIB NIH HHS R01 EB017753NIBIB NIH HHS R01 EB030876NIGMS NIH HHS R35 GM136226
6 · The paper itself

Abstract

Breast cancer becomes invasive when carcinoma cells invade through the basement membrane (BM)-a nanoporous layer of matrix that physically separates the primary tumour from the stroma. Single cells can invade through nanoporous three-dimensional matrices due to protease-mediated degradation or force-mediated widening of pores via invadopodial protrusions. However, how multiple cells collectively invade through the physiological BM, as they do during breast cancer progression, remains unclear. Here we developed a three-dimensional in vitro model of collective invasion of the BM during breast cancer. We show that cells utilize both proteases and forces-but not invadopodia-to breach the BM. Forces are generated from a combination of global cell volume expansion, which stretches the BM, and local contractile forces that act in the plane of the BM to breach it, allowing invasion. These results uncover a mechanism by which cells collectively interact to overcome a critical barrier to metastasis.

Indexed as

Basement MembraneBreast NeoplasmsNeoplasm InvasivenessCell Line, TumorCell SizeFemaleHumans

Identifiers

PMID37957268
PMCPMC11185842
OpenAlexW4388627498

What OpenQuestion holds

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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.