Cited by 203Cellular Mechanics and InteractionsCancer Cells and MetastasisMicrofluidic and Bio-sensing Technologies

Resistance to Fluid Shear Stress Is a Conserved Biophysical Property of Malignant Cells

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Barnes, J. Matthew, Nauseef, Jones T., Henry, Michael D.·2012·PLoS ONE

Abstract

During metastasis, cancer cells enter the circulation in order to gain access to distant tissues, but how this fluid microenvironment influences cancer cell biology is poorly understood. A longstanding view is that circulating cancer cells derived from solid tissues may be susceptible to damage from hemodynamic shear forces, contributing to metastatic inefficiency. Here we report that compared to non-transformed epithelial cells, transformed cells are remarkably resistant to fluid shear stress (FSS) in a microfluidic protocol, exhibiting a biphasic decrease in viability when subjected to a series of millisecond pulses of high FSS. We show that magnitude of FSS resistance is influenced by several oncogenes, is an adaptive and transient response triggered by plasma membrane damage and requires extracellular calcium and actin cytoskeletal dynamics. This novel property of malignant cancer cells may facilitate hematogenous metastasis and indicates, contrary to expectations, that cancer cells are quite resistant to destruction by hemodynamic shear forces.

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  • Cancer cells are more deformable compared to non-cancer cells because of altered membrane composition, and their responsiveness to fluid shear stress differs from that of non-cancer cells.

    “Cancer cells are more deformable compared to non-cancer cells because of their altered membrane composition; consequently, cancer cells’ responsiveness to fluid shear stress has been reported to be different from that of non-cancer cells [32,33,34].”

    From Permeabilizing Cell Membranes with Electric Fields (2021) · cites this paper as [32]

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References 47 · Cited by 203

Authors
Barnes, J. M., Nauseef, J. T., & Henry, M. D.
Affiliations
University of Iowa (US)
Corresponding author
Henry, Michael D.
Venue
PLoS ONE
Published
2012-12-03
Volume
7
Issue
12
Pages
e50973
ISSN
1932-6203 (ISSN-L)
OpenAlex
W2019692639
Cited by
203
References
47
Citations by year
2026: 12 · 2025: 16 · 2024: 21 · 2023: 18 · 2022: 15 · 2021: 23 · 2020: 22 · 2019: 17 · 2018: 18 · 2017: 14 · 2016: 6 · 2015: 14 · 2014: 3 · 2013: 3
FWCI
3.03
Type
journal article
Language
en
Open access
Locations
  • PLoS ONE (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
  • Figshare (submittedVersion, cc-by)
Funders
  • U.S. Department of Defense (W81XWH, W81XWH-12)
  • Brown University
  • Massachusetts Institute of Technology
  • University of California, Irvine
  • Holden Comprehensive Cancer Center, University of Iowa (P30-CA086862)
  • National Cancer Institute (P30CA086862)
  • National Institute of General Medical Sciences (T32GM007337)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
  • Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
  • Physical Sciences › Engineering › Biomedical Engineering › Microfluidic and Bio-sensing Technologies
Keywords
fluid shear stress, shear strength, circulating tumor cells, hematogenous metastasis, oncogenes, cell membrane damage, extracellular calcium, actin cytoskeleton, tumor cell viability
MeSH terms
Actins, Biomechanical Phenomena, Calcium, Cell Membrane, Cell Survival, Cell Transformation, Neoplastic, Extracellular Space, Humans, Models, Biological, Neoplasms, Oncogenes, Rheology, Stress, Mechanical, Cell Death, Cell Line, Tumor, Biophysical Phenomena, Polymerization

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