Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/103735
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Biomedical Engineering | en_US |
| dc.contributor | Research Institute for Smart Ageing | en_US |
| dc.creator | Xin, Y | en_US |
| dc.creator | Li, K | en_US |
| dc.creator | Huang, M | en_US |
| dc.creator | Liang, C | en_US |
| dc.creator | Siemann, D | en_US |
| dc.creator | Wu, L | en_US |
| dc.creator | Tan, Y | en_US |
| dc.creator | Tang, X | en_US |
| dc.date.accessioned | 2024-01-03T05:26:19Z | - |
| dc.date.available | 2024-01-03T05:26:19Z | - |
| dc.identifier.issn | 0950-9232 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/103735 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Nature Publishing Group | en_US |
| dc.rights | © The Author(s) 2023 | en_US |
| dc.rights | Open 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.rights | The 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.title | Biophysics in tumor growth and progression : from single mechano-sensitive molecules to mechanomedicine | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.spage | 3457 | en_US |
| dc.identifier.epage | 3490 | en_US |
| dc.identifier.volume | 42 | en_US |
| dc.identifier.issue | 47 | en_US |
| dc.identifier.doi | 10.1038/s41388-023-02844-x | en_US |
| dcterms.abstract | Evidence 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.accessRights | open access | en_US |
| dcterms.bibliographicCitation | Oncogene, 17 Nov. 2023, v. 42, no. 47, p. 3457-3490 | en_US |
| dcterms.isPartOf | Oncogene | en_US |
| dcterms.issued | 2023-11-17 | - |
| dc.identifier.eissn | 1476-5594 | en_US |
| dc.description.validate | 202401 bcch | en_US |
| dc.description.oa | Version of Record | en_US |
| dc.identifier.FolderNumber | a2557, a3058 | - |
| dc.identifier.SubFormID | 47869, 49305 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.description.oaCategory | CC | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| s41388-023-02844-x.pdf | 3.42 MB | Adobe PDF | View/Open |
Page views
129
Citations as of Nov 10, 2025
Downloads
64
Citations as of Nov 10, 2025
SCOPUSTM
Citations
7
Citations as of Jun 21, 2024
WEB OF SCIENCETM
Citations
57
Citations as of Dec 18, 2025
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



