Polyploidy of MDA-MB-231 cells drives increased extravasation with enhanced cell-matrix adhesion

被引:0
|
作者
Hirose, Satomi [1 ]
Osaki, Tatsuya [2 ,3 ]
Kamm, Roger D. [1 ,4 ]
机构
[1] MIT, Dept Mech Engn, Cambridge, MA 02139 USA
[2] MIT, Picower Inst Learning & Memory, Cambridge, MA 02139 USA
[3] MIT, WHITEHEAD INST, CAMBRIDGE, MA 02139 USA
[4] MIT, Dept Biol Engn, Cambridge, MA 02139 USA
来源
APL BIOENGINEERING | 2025年 / 9卷 / 01期
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER; DNA METHYLATION; IN-VITRO; VIMENTIN; MECHANISMS; ANEUPLOIDY; DYNAMICS; TUMORIGENESIS; INVASIVENESS;
D O I
10.1063/5.0233329
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Metastasis, the leading cause of cancer-related deaths, involves a complex cascade of events, including extravasation. Despite extensive research into metastasis, the mechanisms underlying extravasation remain unclear. Molecular targeted therapies have advanced cancer treatment, yet their efficacy is limited, prompting exploration into novel therapeutic targets. Here, we showed the association of polyploidy in MDA-MB-231 breast cancer cells and their extravasation, using microfluidic systems to reproduce the in vivo microvascular environment. We observed enhanced extravasation in polyploid cells alongside upregulated expression of genes involved in cell-substrate adhesion and cell mechanical dynamics. These findings offer insights into the relationship between polyploidy and extravasation, highlighting potential targets for cancer therapy. (c) 2025 Author(s). All article content, except where otherwise noted, is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International (CC BY-NC-ND) license (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:11
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