The dynamic tumor extracellular matrix: Biophysical cues, cellular crosstalk, and disease progression

dc.contributor.authorJoshi, Omkar
dc.contributor.authorHamidi, Hellyeh
dc.contributor.authorMathieu, Mathilde
dc.contributor.authorIvaska, Johanna
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organizationfi=Turun biotiedekeskus|en=Turku Bioscience Centre|
dc.contributor.organizationfi=biokemia|en=Biochemistry|
dc.contributor.organizationfi=InFLAMES Lippulaiva|en=InFLAMES Flagship|
dc.contributor.organization-code1.2.246.10.2458963.20.18586209670
dc.contributor.organization-code1.2.246.10.2458963.20.49728377729
dc.contributor.organization-code1.2.246.10.2458963.20.68445910604
dc.converis.publication-id515864016
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/515864016
dc.date.accessioned2026-04-24T20:11:53Z
dc.description.abstract<p>The interplay between diverse cell types and their extracellular matrix (ECM) is fundamental for multicellular life. The ECM is a complex meshwork of fibrillar proteins and soluble factors. Cells and their surrounding ECM interact bidirectionally, whereby cells deposit their tissue-specific ECM and remodel it enzymatically and by exerting contractile forces. The ECM in turn modulates cellular functions like gene expression, proliferation, and motility. A careful balance of this interaction is key for homeostasis, and is lost during cancer progression. Different cell types constituting a tumor including cancer and stromal cells, contribute to an imbalanced cell-ECM crosstalk within the tumor. Cumulatively, this leads to a tumor ECM characterized by particular features like increased stiffness and viscoelasticity, altered alignment, bundled fibers, etc. In this review, we discuss the advances in our understanding of the tumor ECM architecture and the multicellular interactions that help achieve it, with a special focus on increasing granularity in disentangling the contributions of individual tumor ECM features in disease progression.<br></p>
dc.identifier.eissn2468-4511
dc.identifier.urihttps://www.utupub.fi/handle/11111/59447
dc.identifier.urlhttps://doi.org/10.1016/j.cobme.2026.100652
dc.identifier.urnURN:NBN:fi-fe2026042333219
dc.language.isoen
dc.okm.affiliatedauthorJoshi, Omkar
dc.okm.affiliatedauthorHamidi, Hellyeh
dc.okm.affiliatedauthorMathieu, Mathilde
dc.okm.affiliatedauthorIvaska, Johanna
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3111 Biomedicineen_GB
dc.okm.discipline3111 Biolääketieteetfi_FI
dc.okm.discipline3122 Cancersen_GB
dc.okm.discipline3122 Syöpätauditfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA2 Scientific Article
dc.publisherElsevier BV
dc.publisher.countryUnited Kingdomen_GB
dc.publisher.countryBritanniafi_FI
dc.publisher.country-codeGB
dc.relation.articlenumber100652
dc.relation.doi10.1016/j.cobme.2026.100652
dc.relation.ispartofjournalCurrent opinion in biomedical engineering
dc.relation.volume38
dc.titleThe dynamic tumor extracellular matrix: Biophysical cues, cellular crosstalk, and disease progression
dc.year.issued2026

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