Evidence map›Paper›PMID 38169188›Full record

ArticleBiomaterials2024

Emergence of nanoscale viscoelasticity from single cancer cells to established tumors.

Muhamed Hadzipasic, Sue Zhang, Zhuoying Huang, Rachel Passaro, Margaret S Sten, Ganesh M Shankar, Hadi T Nia

Open access · greenAbstract read
In one paragraph

Article in Biomaterials, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

11 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
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  4. Review
  5. Solid Stress Estimations via Intraoperative 3D Navigation in Patients with Brain Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  6. High-Throughput Nanorheology of Living Cells Powered by Supervised Machine Learning.Advanced intelligent systems (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  7. 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

7 authors at 2 institutions in 1 country.

Muhamed HadzipasicDepartment of Biomedical Engineering, Boston University Boston, MA, USA; Department of Neurosurgery, Massachusetts General Hospital, Harvard Medical School Boston, Massachusetts, USA.
Sue ZhangDepartment of Biomedical Engineering, Boston University Boston, MA, USA.
Zhuoying HuangDepartment of Biomedical Engineering, Boston University Boston, MA, USA.
Rachel PassaroDepartment of Biomedical Engineering, Boston University Boston, MA, USA.
Margaret S StenDepartment of Neurosurgery, Massachusetts General Hospital, Harvard Medical School Boston, Massachusetts, USA.
Ganesh M ShankarDepartment of Neurosurgery, Massachusetts General Hospital, Harvard Medical School Boston, Massachusetts, USA.
Hadi T NiaDepartment of Biomedical Engineering, Boston University Boston, MA, USA. Electronic address: htnia@bu.edu.
Boston University · USHarvard University · US

Funding

Translational Research in BiomaterialsT32EB006359 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI MARK W. GRINSTAFF, Michelle H Teplensky · 2009 to 2026
$4.2M
Probing functioning lung at the cellular resolution in health and diseaseDP2HL168562 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NIA, HADI TAVAKOLI · 2022 to 2025
$2.5M
Classifying malignant pulmonary nodules using biophysics-enhanced artificial intelligenceR21EB031332 · NIBIB · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NIA, HADI TAVAKOLI · 2021 to 2021
$660k
NHLBI NIH HHS DP2 HL168562NIBIB NIH HHS R21 EB031332NIBIB NIH HHS T32 EB006359
6 · The paper itself

Abstract

Tumors are complex materials whose physical properties dictate growth and treatment outcomes. Recent evidence suggests time-dependent physical properties, such as viscoelasticity, are crucial, distinct mechanical regulators of cancer progression and malignancy, yet the genesis and consequences of tumor viscoelasticity are poorly understood. Here, using Wide-bandwidth AFM-based ViscoElastic Spectroscopy (WAVES) coupled with mathematical modeling, we probe the origins of tumor viscoelasticity. From single carcinoma cells to increasingly sized carcinoma spheroids to established tumors, we describe a stepwise evolution of dynamic mechanical properties that create a nanorheological signature of established tumors: increased stiffness, decreased rate-dependent stiffening, and reduced energy dissipation. We dissect this evolution of viscoelasticity by scale, and show established tumors use fluid-solid interactions as the dominant mechanism of mechanical energy dissipation as opposed to fluid-independent intrinsic viscoelasticity. Additionally, we demonstrate the energy dissipation mechanism in spheroids and established tumors is negatively correlated with the cellular density, and this relationship strongly depends on an intact actin cytoskeleton. These findings define an emergent and targetable signature of the physical tumor microenvironment, with potential for deeper understanding of tumor pathophysiology and treatment strategies.

Indexed as

CarcinomaModels, BiologicalActin CytoskeletonElasticityHumansTumor MicroenvironmentViscosity

Identifiers

PMID38169188
PMCPMC10837793
OpenAlexW4390101771

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.