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Mechanical interactions of invasive cancer cells through their substrate evolve from additive to synergistic
by
Wiener, Guy I.
, Weihs, Daphne
, Kadosh, Dana
in
Breast cancer
/ Cancer
/ Cancer cell
/ Cancer invasion
/ Cell adhesion
/ Cell Communication
/ Cell culture
/ Cell Line, Tumor
/ Cell Movement
/ Collagen
/ Evolution
/ Gels
/ Humans
/ Invasiveness
/ Mechanical Phenomena
/ Mechanical stimuli
/ Metastases
/ Metastasis
/ Microscopy
/ Neoplasm Invasiveness
/ Pleural effusion
/ Stiffness
/ Strain energy
/ Substrates
/ Three-dimensional traction microscopy
/ Time dependence
2021
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Mechanical interactions of invasive cancer cells through their substrate evolve from additive to synergistic
by
Wiener, Guy I.
, Weihs, Daphne
, Kadosh, Dana
in
Breast cancer
/ Cancer
/ Cancer cell
/ Cancer invasion
/ Cell adhesion
/ Cell Communication
/ Cell culture
/ Cell Line, Tumor
/ Cell Movement
/ Collagen
/ Evolution
/ Gels
/ Humans
/ Invasiveness
/ Mechanical Phenomena
/ Mechanical stimuli
/ Metastases
/ Metastasis
/ Microscopy
/ Neoplasm Invasiveness
/ Pleural effusion
/ Stiffness
/ Strain energy
/ Substrates
/ Three-dimensional traction microscopy
/ Time dependence
2021
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Mechanical interactions of invasive cancer cells through their substrate evolve from additive to synergistic
by
Wiener, Guy I.
, Weihs, Daphne
, Kadosh, Dana
in
Breast cancer
/ Cancer
/ Cancer cell
/ Cancer invasion
/ Cell adhesion
/ Cell Communication
/ Cell culture
/ Cell Line, Tumor
/ Cell Movement
/ Collagen
/ Evolution
/ Gels
/ Humans
/ Invasiveness
/ Mechanical Phenomena
/ Mechanical stimuli
/ Metastases
/ Metastasis
/ Microscopy
/ Neoplasm Invasiveness
/ Pleural effusion
/ Stiffness
/ Strain energy
/ Substrates
/ Three-dimensional traction microscopy
/ Time dependence
2021
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Mechanical interactions of invasive cancer cells through their substrate evolve from additive to synergistic
Journal Article
Mechanical interactions of invasive cancer cells through their substrate evolve from additive to synergistic
2021
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Overview
Non-contacting, adjacent cancer cells can mechanically interact through their substrate to increase their invasive and migratory capacities that underly metastases-formation. Such mechanical interactions may induce additive or synergistic enhancement of invasiveness, potentially indicating different underlying force-mechanisms. To identify cell–cell-gel interactions, we monitor the time-evolution of three-dimensional traction strains induced by MDA-MB-231 breast cancer cells adhering on physiological-stiffness (1.8 kPa) collagen gels and compare to simulations. Single metastatic cells apply strain energies of 0.2–2 pJ (average 0.51 ± 0.06 pJ) at all observation times (30–174 min) inducing a mechanical volume-of-effect in the collagen gel that is initially (<60 min from seeding) on the cell-volume scale (∼3000 µm3) and on average increases with time from cell seeding. When cells adhere closely adjacent, at short times (<60 min) we distinguish the additive contributions of neighboring cells to the strains, while at longer times strain fields are synergistically amplified and may facilitate increased cooperative/collective cancer-cell-invasiveness. The results of well-spaced and closely adjacent cells at short times match our simulations of additive deformations induced by radially applied strains with experimentally based inverse-distance decay. We thus reveal a time-dependent evolution from additive to synergistic interactions of adjacently adhering cells that may facilitate metastatic invasion.
Publisher
Elsevier Ltd,Elsevier Limited
Subject
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