Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/49000
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dc.contributor.authorShaghoury, Amir-
dc.contributor.authorDadon, Sapir-
dc.contributor.authorWEIHS, Daphne-
dc.date.accessioned2026-05-07T12:56:12Z-
dc.date.available2026-05-07T12:56:12Z-
dc.date.issued2026-
dc.date.submitted2026-04-24T12:39:21Z-
dc.identifier.citationACS biomaterials science & engineering, 12 (4) , p. 2457 -2466-
dc.identifier.urihttp://hdl.handle.net/1942/49000-
dc.description.abstractMetastasis, 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.-
dc.description.sponsorshipThe authors thank Ms. Ekaterina Gurevich and Ms. Yael Diamant for their assistance with the gel-mechanics character ization. The work was partially supported by the Israeli Ministry of Science and Technology (MOST) Breakthrough research program (Grant no. 1001717860 awarded to Professor Daphne Weihs), by the Applebaum Foundation and by the Gerald O. Mann and the Frank and Dolores Corbett Charitable Foundations (all awarded to Professor Daphne Weihs)-
dc.language.isoen-
dc.publisherAMER CHEMICAL SOC-
dc.rights2026 The Authors. Published by American Chemical Society. This article is licensed under CC-BY 4.0-
dc.subject.othermechanobiology-
dc.subject.othercancer cell invasiveness-
dc.subject.otherinvasiveforces-
dc.subject.othercytoskeleton-
dc.subject.otherfinite element modeling-
dc.titleEffects of Intracellular Force Localization on Cancer Cell Invasion: Revealing Mechanical Trade-offs through Experimentally Validated Computational Models-
dc.typeJournal Contribution-
dc.identifier.epage2466-
dc.identifier.issue4-
dc.identifier.spage2457-
dc.identifier.volume12-
local.format.pages10-
local.bibliographicCitation.jcatA1-
dc.description.notesWeihs, 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.-
dc.description.notesdaphnew@technion.ac.il-
local.publisher.place1155 16TH ST, NW, WASHINGTON, DC 20036 USA-
local.type.refereedRefereed-
local.type.specifiedArticle-
dc.identifier.doi10.1021/acsbiomaterials.6c00194-
dc.identifier.pmid41795681-
dc.identifier.isi001709108100001-
local.provider.typewosris-
local.description.affiliation[Shaghoury, Amir; Dadon, Sapir; Weihs, Daphne] Technion Israel Inst Technol, Fac Biomed Engn, IL-3200003 Haifa, Israel; [Weihs, Daphne] Hasselt Univ, Fac Sci, Dept Math & Stat, B-3590 Diepenbeek, Belgium; [Weihs, Daphne] Hasselt Univ, Data Sci Inst, Fac Sci, B-3590 Diepenbeek, Belgium-
local.uhasselt.internationalno-
item.fulltextWith Fulltext-
item.fullcitationShaghoury, Amir; Dadon, Sapir & WEIHS, Daphne (2026) Effects of Intracellular Force Localization on Cancer Cell Invasion: Revealing Mechanical Trade-offs through Experimentally Validated Computational Models. In: ACS biomaterials science & engineering, 12 (4) , p. 2457 -2466.-
item.accessRightsOpen Access-
item.contributorShaghoury, Amir-
item.contributorDadon, Sapir-
item.contributorWEIHS, Daphne-
crisitem.journal.issn2373-9878-
crisitem.journal.eissn2373-9878-
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