Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/103735
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dc.contributorDepartment of Biomedical Engineeringen_US
dc.contributorResearch Institute for Smart Ageingen_US
dc.creatorXin, Yen_US
dc.creatorLi, Ken_US
dc.creatorHuang, Men_US
dc.creatorLiang, Cen_US
dc.creatorSiemann, Den_US
dc.creatorWu, Len_US
dc.creatorTan, Yen_US
dc.creatorTang, Xen_US
dc.date.accessioned2024-01-03T05:26:19Z-
dc.date.available2024-01-03T05:26:19Z-
dc.identifier.issn0950-9232en_US
dc.identifier.urihttp://hdl.handle.net/10397/103735-
dc.language.isoenen_US
dc.publisherNature Publishing Groupen_US
dc.rights© The Author(s) 2023en_US
dc.rightsOpen Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.en_US
dc.rightsThe following publication Xin, Y., Li, K., Huang, M. et al. Biophysics in tumor growth and progression: from single mechano-sensitive molecules to mechanomedicine. Oncogene 42, 3457–3490 (2023) is available at https://doi.org/10.1038/s41388-023-02844-x.en_US
dc.titleBiophysics in tumor growth and progression : from single mechano-sensitive molecules to mechanomedicineen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage3457en_US
dc.identifier.epage3490en_US
dc.identifier.volume42en_US
dc.identifier.issue47en_US
dc.identifier.doi10.1038/s41388-023-02844-xen_US
dcterms.abstractEvidence from physical sciences in oncology increasingly suggests that the interplay between the biophysical tumor microenvironment and genetic regulation has significant impact on tumor progression. Especially, tumor cells and the associated stromal cells not only alter their own cytoskeleton and physical properties but also remodel the microenvironment with anomalous physical properties. Together, these altered mechano-omics of tumor tissues and their constituents fundamentally shift the mechanotransduction paradigms in tumorous and stromal cells and activate oncogenic signaling within the neoplastic niche to facilitate tumor progression. However, current findings on tumor biophysics are limited, scattered, and often contradictory in multiple contexts. Systematic understanding of how biophysical cues influence tumor pathophysiology is still lacking. This review discusses recent different schools of findings in tumor biophysics that have arisen from multi-scale mechanobiology and the cutting-edge technologies. These findings range from the molecular and cellular to the whole tissue level and feature functional crosstalk between mechanotransduction and oncogenic signaling. We highlight the potential of these anomalous physical alterations as new therapeutic targets for cancer mechanomedicine. This framework reconciles opposing opinions in the field, proposes new directions for future cancer research, and conceptualizes novel mechanomedicine landscape to overcome the inherent shortcomings of conventional cancer diagnosis and therapies.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationOncogene, 17 Nov. 2023, v. 42, no. 47, p. 3457-3490en_US
dcterms.isPartOfOncogeneen_US
dcterms.issued2023-11-17-
dc.identifier.eissn1476-5594en_US
dc.description.validate202401 bcchen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumbera2557, a3058-
dc.identifier.SubFormID47869, 49305-
dc.description.fundingSourceRGCen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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