Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/49000
Title: Effects of Intracellular Force Localization on Cancer Cell Invasion: Revealing Mechanical Trade-offs through Experimentally Validated Computational Models
Authors: Shaghoury, Amir
Dadon, Sapir
WEIHS, Daphne 
Issue Date: 2026
Publisher: AMER CHEMICAL SOC
Source: ACS biomaterials science & engineering, 12 (4) , p. 2457 -2466
Abstract: Metastasis, leading to 90% of cancer-related deaths, is driven by invasive forces exerted by cancer cells on their microenvironment. While actin is central to force generation and motility, the effects of intracellular force-localization during invasion remain largely unexplored. We previously demonstrated, in a clinically relevant assay, invasive cancer cells indenting soft, elastic gels to cell-scale depths, and developed corresponding experimentally validated finite element models. Here, we applied those models to investigate how the force-application location, above (top) or below (bottom) the nucleus, affects invasion efficiency. Under low force-levels (<= 100 nN), top-applied forces produce 35-42% deeper indentations than bottom-applied forces, with modest increases in intracellular stress, indicating potentially increased invasiveness. However, with top-applied forces, similar to 10% less stress is transmitted to the gel, suggesting less effective microenvironmental mechanical interaction. In contrast, under higher forces (>= 150 nN), bottom-applied forces become more effective, transmitting >15% more stress to the gel, with indentation depths becoming comparable between top- and bottom-applied configurations, and significantly (>250%) less nuclear stress generated, thereby supporting invasion. These trends are particularly evident when the cytoplasm is softer than the nucleus, as is typical of (invasive cancer) cells. Thus, top-applied forces may support shallow invasion into soft environments, whereas bottom-applied forces mimicking actin-rich, stiff, leading-edge protrusions, optimize deep, forceful invasion with reduced cell-integrity risk. We demonstrate that intracellular force-localization critically influences the mechanical trade-offs between invasion efficiency and cellular stability, potentially offering targets for antimetastatic strategies.
Notes: Weihs, D (corresponding author), Technion Israel Inst Technol, Fac Biomed Engn, IL-3200003 Haifa, Israel.; Weihs, D (corresponding author), Hasselt Univ, Fac Sci, Dept Math & Stat, B-3590 Diepenbeek, Belgium.; Weihs, D (corresponding author), Hasselt Univ, Data Sci Inst, Fac Sci, B-3590 Diepenbeek, Belgium.
daphnew@technion.ac.il
Keywords: mechanobiology;cancer cell invasiveness;invasiveforces;cytoskeleton;finite element modeling
Document URI: http://hdl.handle.net/1942/49000
ISSN: 2373-9878
e-ISSN: 2373-9878
DOI: 10.1021/acsbiomaterials.6c00194
ISI #: 001709108100001
Rights: 2026 The Authors. Published by American Chemical Society. This article is licensed under CC-BY 4.0
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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