The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.
Collective Cell Migration
Abstract
For all animals, cell migration is an essential and highly regulated process. Cells migrate to shape tissues, to vascularize tissues, in wound healing, and as part of the immune response. Unfortunately, tumor cells can also become migratory and invade surrounding tissues. Some cells migrate as individuals, but many cell types will, under physiological conditions, migrate collectively in tightly or loosely associated groups. This includes invasive tumor cells. This review discusses different types of collective cell migration, including sheet movement, sprouting and branching, streams, and free groups, and highlights recent findings that provide insight into cells' organization and behavior. Cells performing collective migration share many cell biological characteristics with independently migrating cells but, by affecting one another mechanically and via signaling, these cell groups are subject to additional regulation and constraints. New properties that emerge from this connectivity can contribute to shaping, guiding, and ultimately ensuring tissue function.
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Citations
Cites
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“Interestingly, this function can be provided by normal stromal fibroblasts, which can be recruited by tumor cells (Gaggioli et al. 2007).”
BackgroundInhibition of Dll4 signalling inhibits tumour growth by deregulating angiogenesis
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Building epithelial architecture: insights from three-dimensional culture models
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Conserved Patterns of Cell Movements during Vertebrate Gastrulation
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Cited by
Vinci, M., Gowan, S., Boxall, F., Patterson, L., Zimmermann, M., Court, W., Lomas, C., Mendiola, M., Hardisson, D., & Eccles, S. A. (2012) · BMC Biology · doi:10.1186/1741-7007-10-29 · Cited by 1,024
Classifying collective cancer cell invasion
Friedl, P., Locker, J., Sahai, E., & Segall, J. E. (2012) · Nature Cell Biology · doi:10.1038/ncb2548 · Cited by 963
In Vitro Tumor Models: Advantages, Disadvantages, Variables, and Selecting the Right Platform
Katt, M. E., Placone, A. L., Wong, A. D., Xu, Z. S., & Searson, P. C. (2016) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2016.00012 · Cited by 754
Karagiannis, G. S., Poutahidis, T., Erdman, S. E., Kirsch, R., Riddell, R. H., & Diamandis, E. P. (2012) · Molecular Cancer Research · doi:10.1158/1541-7786.mcr-12-0307 · Cited by 507
Complement Fragment C3a Controls Mutual Cell Attraction during Collective Cell Migration
Carmona-Fontaine, C., Theveneau, E., Tzekou, A., Tada, M., Woods, M., Page, K. M., Parsons, M., Lambris, J. D., & Mayor, R. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.10.012 · Cited by 317
Metadata
- Authors
- Rørth, P.
- Venue
- Annual Review of Cell and Developmental Biology
- Publisher
- Annual Reviews
- Published
- 2009-11-01
- Volume
- 25
- Issue
- 1
- Pages
- 407-429
- ISSN
- 1081-0706 (ISSN-L)
- 1530-8995
- OpenAlex
- W2132756167
- Cited by
- 599
- References
- 7
- FWCI
- 1.78
- Type
- journal article
- Language
- en
- Open access
- closed
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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.
Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
