» Articles » PMID: 19707854

The Molecular Mechanisms of Transition Between Mesenchymal and Amoeboid Invasiveness in Tumor Cells

Overview
Publisher Springer
Specialty Biology
Date 2009 Aug 27
PMID 19707854
Citations 158
Authors
Affiliations
Soon will be listed here.
Abstract

Tumor cells exhibit at least two distinct modes of migration when invading the 3D environment. A single tumor cell's invasive strategy follows either mesenchymal or amoeboid patterns. Certain cell types can use both modes of invasiveness and undergo transitions between them. This work outlines the signaling pathways involved in mesenchymal and amoeboid types of tumor cell motility and summarizes the molecular mechanisms that are involved in transitions between them. The focus is on the signaling of the Rho family of small GTPases that regulate the cytoskeleton-dependent processes taking place during the cell migration. The multiple interactions among the Rho family of proteins, their regulators and effectors are thought to be the key determinants of the particular type of invasiveness. Mesenchymal and amoeboid invasive strategies display different adhesive and proteolytical interactions with the surrounding matrix and the alterations influencing these interactions can also lead to the transitions.

Citing Articles

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

Hirose S, Osaki T, Kamm R APL Bioeng. 2025; 9(1):016105.

PMID: 39974511 PMC: 11836873. DOI: 10.1063/5.0233329.


CD44 and Ezrin restrict EGF receptor mobility to generate a novel spatial arrangement of cytoskeletal signaling modules driving bleb-based migration.

Jha A, Chandra A, Farahani P, Toettcher J, Haugh J, Waterman C bioRxiv. 2025; .

PMID: 39803565 PMC: 11722407. DOI: 10.1101/2024.12.31.630838.


Multicellular model of neuroblastoma proposes unconventional therapy based on multiple roles of p53.

Wertheim K, Chisholm R, Richmond P, Walker D PLoS Comput Biol. 2024; 20(12):e1012648.

PMID: 39715281 PMC: 11723635. DOI: 10.1371/journal.pcbi.1012648.


Representing ECM composition and EMT pathways in gastric cancer using a new metastatic gene signature.

Albano F, Russi S, Laurino S, Mazzone P, Di Paola G, Zoppoli P Front Cell Dev Biol. 2024; 12:1481818.

PMID: 39563861 PMC: 11573575. DOI: 10.3389/fcell.2024.1481818.


An allosteric inhibitor of RhoGAP class-IX myosins suppresses the metastatic features of cancer cells.

Kyriazi D, Voth L, Bader A, Ewert W, Gerlach J, Elfrink K Nat Commun. 2024; 15(1):9947.

PMID: 39550360 PMC: 11569205. DOI: 10.1038/s41467-024-54181-6.


References
1.
Rosel D, Brabek J, Tolde O, Mierke C, Zitterbart D, Raupach C . Up-regulation of Rho/ROCK signaling in sarcoma cells drives invasion and increased generation of protrusive forces. Mol Cancer Res. 2008; 6(9):1410-20. DOI: 10.1158/1541-7786.MCR-07-2174. View

2.
Amano M, Ito M, Kimura K, Fukata Y, Chihara K, Nakano T . Phosphorylation and activation of myosin by Rho-associated kinase (Rho-kinase). J Biol Chem. 1996; 271(34):20246-9. DOI: 10.1074/jbc.271.34.20246. View

3.
Mandeville J, Lawson M, Maxfield F . Dynamic imaging of neutrophil migration in three dimensions: mechanical interactions between cells and matrix. J Leukoc Biol. 1997; 61(2):188-200. DOI: 10.1002/jlb.61.2.188. View

4.
Gadea G, Lapasset L, Gauthier-Rouviere C, Roux P . Regulation of Cdc42-mediated morphological effects: a novel function for p53. EMBO J. 2002; 21(10):2373-82. PMC: 126005. DOI: 10.1093/emboj/21.10.2373. View

5.
Pinner S, Sahai E . PDK1 regulates cancer cell motility by antagonising inhibition of ROCK1 by RhoE. Nat Cell Biol. 2008; 10(2):127-37. DOI: 10.1038/ncb1675. View