Evidence map›Paper›PMID 39448802›Full record

ArticleNature cell biology2024

Differential stiffness between brain vasculature and parenchyma promotes metastatic infiltration through vessel co-option.

Marina Uroz, Amy E Stoddard, Bryan P Sutherland, Olivia Courbot, Roger Oria, Linqing Li, Cara R Ravasio, Mai T Ngo, Jinling Yang, Juliann B Tefft and 5 more

Abstract read
In one paragraph

Article in Nature cell biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Mechanical regulation of cell memory.Nature structural & molecular biology · 2026
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  8. Understanding Glioblastoma Dynamics Using 3D Organoids and Engineered Extracellular Matrix.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

15 authors.

Marina UrozDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID 0000-0003-4124-8048
Amy E StoddardDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Bryan P SutherlandDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Olivia CourbotCell and Tissue Mechanobiology Laboratory, The Francis Crick Institute, London, UK.ORCID 0000-0003-4363-3249
Roger OriaDepartment of Surgery, University of California, San Francisco, CA, USA.ORCID 0000-0002-5974-9775
Linqing LiDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Cara R RavasioDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Mai T NgoDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Jinling YangDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Juliann B TefftDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID 0000-0002-8826-665X
Jeroen EyckmansDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.ORCID 0000-0003-1475-8149
Xue HanDepartment of Biomedical Engineering, Boston University, Boston, MA, USA.
Alberto Elosegui-ArtolaCell and Tissue Mechanobiology Laboratory, The Francis Crick Institute, London, UK.ORCID 0000-0003-0644-3294
Valerie M WeaverDepartment of Surgery, University of California, San Francisco, CA, USA.ORCID 0000-0003-4786-6752
Christopher S ChenDepartment of Biomedical Engineering, Boston University, Boston, MA, USA. chencs@bu.edu.ORCID 0000-0003-2445-8449

Funding

Tissue mechanics reprograms the tissue to malignancy and metastasisR35CA242447 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VALERIE MARIE WEAVER · 2020 to 2026
$6.6M
Translational Research in BiomaterialsT32EB006359 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MARK W. GRINSTAFF, Michelle H Teplensky · 2009 to 2026
$4.2M
A physical sciences approach to investigate the role of exosomes in metastatic progressionU01CA250044 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GUO, WEI, RADHAKRISHNAN, RAVI · 2021 to 2025
$3.9M
Organ Design and Engineering Training Program (ODET Program)T32EB016652 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI BONVENTRE, JOSEPH VINCENT · 2014 to 2023
$3.5M
Synthetic vascularization and regeneration in engineered tissuesR01EB033821 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI SANGEETA N. BHATIA, CHRISTOPHER S CHEN · 2023 to 2026
$2.2M
Development of a wound-on-chip model to study stromal-epithelial interactions during tissue repairR21EB028491 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI EYCKMANS, JEROEN · 2020 to 2022
$660k
Developing a Temporally-Regulated Gene Therapy for Therapeutic AngiogenesisF32HL165691 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NGO, MAI · 2022 to 2023
$137k
American Heart Association (American Heart Association, Inc.) postdoctoral fellowship (828475)European Molecular Biology Organization (EMBO) EMBO ALTF811-2018National Science Foundation (NSF) 2021324226National Science Foundation (NSF) CMMI-1548571National Science Foundation (NSF) Graduate Research Fellowship (1745302 and 2141064)NCI NIH HHS R35 CA242447NCI NIH HHS U01 CA250044NHLBI NIH HHS F32 HL165691NIBIB NIH HHS R01 EB033821NIBIB NIH HHS R21 EB028491NIBIB NIH HHS T32 EB006359NIBIB NIH HHS T32 EB016652U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) CA242447-01U.S. Department of Health & Human Services | NIH | National Heart, Lung, and Blood Institute (NHLBI) NIH NHLBI 1F32HL165691U.S. Department of Health & Human Services | NIH | National Institute of Biomedical Imaging and Bioengineering (NIBIB) EB033821Wellcome Trust CC2214
6 · The paper itself

Abstract

In brain metastasis, cancer cells remain in close contact with the existing vasculature and can use vessels as migratory paths-a process known as vessel co-option. However, the mechanisms regulating this form of migration are poorly understood. Here we use ex vivo brain slices and an organotypic in vitro model for vessel co-option to show that cancer cell invasion along brain vasculature is driven by the difference in stiffness between vessels and the brain parenchyma. Imaging analysis indicated that cells move along the basal surface of vessels by adhering to the basement membrane extracellular matrix. We further show that vessel co-option is enhanced by both the stiffness of brain vasculature, which reinforces focal adhesions through a talin-dependent mechanism, and the softness of the surrounding environment that permits cellular movement. Our work reveals a mechanosensing mechanism that guides cell migration in response to the tissue's intrinsic mechanical heterogeneity, with implications in cancer invasion and metastasis.

Indexed as

BrainBrain NeoplasmsCell MovementNeoplasm InvasivenessAnimalsBasement MembraneCell AdhesionCell Line, TumorExtracellular MatrixFemaleFocal AdhesionsHumansMechanotransduction, CellularMiceNeoplasm MetastasisNeovascularization, PathologicTalin

Identifiers

PMID39448802
PMCPMC12233033

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Registered trials

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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.