Actin dynamics during tumor cell dissemination
Open accessAbstract
The actin cytoskeleton is a dynamic network that regulates cellular behavior from development to disease. By rearranging the actin cytoskeleton, cells are capable of migrating and invading during developmental processes; however, many of these cellular properties are hijacked by cancer cells to escape primary tumors and disseminate to distant organs in the body. In this review article, we highlight recent work describing how cancer cells regulate the actin cytoskeleton to achieve efficient invasion and metastatic colonization. We also review new imaging technologies that are capable of revealing the complex architecture and regulation of the actin cytoskeleton during motility and invasion of tumor cells.
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The ARP2/3 complex is a critical mediator of the entire metastatic cascade, from migration to invasion and in vivo metastatic spread.
“The ARP2/3 complex is a critical mediator of the entire metastatic cascade; from migration to invasion and in vivo metastatic spread (Molinie & Gautreau, 2018, Mondal et al., 2021).”
From SHARPIN S146 phosphorylation mediates ARP2/3 interaction, cancer cell invasion and metastasis (2022) · cites this paper as Mondal et al., 2021
The Lamellipodia section (page unavailable) describes Arp2/3 activation as a mechanism that generates protrusions driving cancer-cell migration. It also discusses invasion through related actin-regulatory complexes, but does not establish that Arp2/3 itself is a critical mediator of the entire metastatic cascade or of in vivo metastatic spread. (LLM, conf=0.85)
Experimental — accuracy not yet measuredARP2/3-dependent lamellipodia formation promotes cell migration and invasion.
“ARP2/3-dependent lamellipodia formation promotes cell migration and invasion (Molinie & Gautreau, 2018, Mondal et al., 2021, Suraneni, Rubinstein et al., 2012).”
From SHARPIN S146 phosphorylation mediates ARP2/3 interaction, cancer cell invasion and metastasis (2022) · cites this paper as Mondal et al., 2021
The Lamellipodia section (page unavailable) says lamellipodia can drive cancer-cell migration and describes Arp2/3 activation as a mechanism of their formation. It also says lamellipodin supports lamellipodial protrusion and can promote 3D invasion, but does not specifically say that Arp2/3-dependent lamellipodia formation promotes invasion. (LLM, conf=0.82)
Experimental — accuracy not yet measured
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Three-dimensional microfluidic model for tumor cell intravasation and endothelial barrier function
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Phenotype plasticity as enabler of melanoma progression and therapy resistance
Arozarena, I., & Wellbrock, C. (2019) · Nature Reviews Cancer · doi:10.1038/s41568-019-0154-4 · Cited by 381 · cited 1× · see citing works
“In melanoma, tumor cells are able to switch between a high-proliferative/low invasive state to a low-proliferative/high invasive state, known as phenotype switching, as the disease progresses (Arozarena and Wellbrock, 2019).”
BackgroundMechanisms and impact of altered tumour mechanics
Mohammadi, H., & Sahai, E. (2018) · Nature Cell Biology · doi:10.1038/s41556-018-0131-2 · Cited by 336 · see citing works
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Sorted by citations
SHARPIN S146 phosphorylation mediates ARP2/3 interaction, cancer cell invasion and metastasis
Butt, U., Khan, M. H., Pouwels, J., & Westermarck, J. (2022) · Journal of Cell Science · doi:10.1242/jcs.260627 · Cited by 6 · see citing works
SHARPIN serine 146 phosphorylation mediates ARP2/3 interaction, cancer cell invasion and metastasis
Butt, U., Khan, M. H., Pouwels, J., & Westermarck, J. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.01.21.477220 · Cited by 6 · see citing works
“Constitutive SHARPIN S146 phosphorylation contributes to lamellipodium formation ARP2/3-dependent lamellipodia formation promotes cell migration and invasion (Molinie & Gautreau, 2018, Mondal et al., 2021, Suraneni, Rubinstein et al., 2012).”
Background
- Authors
- Mondal, C., Martino, J. S. D., & Bravo‐Cordero, J. J.
- Affiliations
- Tisch Cancer Institute (US)
- Corresponding author
- Jose Javier Bravo‐Cordero
- Venue
- International Review of Cell and Molecular Biology
- Publisher
- Elsevier
- Published
- 2021
- Volume
- 360
- Pages
- 65-98
- ISSN
- 0074-7696 (ISSN-L)
- 1937-6448
- PMC
- PMC8246644
- OpenAlex
- W3109327701
- Cited by
- 39
- References
- 4
- Citations by year
- 2026: 7 · 2025: 6 · 2024: 12 · 2023: 10 · 2022: 3 · 2021: 1
- FWCI
- 5.81
- Type
- book chapter
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- International review of cytology (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (CA244780, K22CA196750)
- Adenoid Cystic Carcinoma Research Foundation
- National Institutes of Health (T32 CA078207)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular Mechanics and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mechanisms of cancer metastasis
- Health Sciences › Medicine › Oncology › Cancer Cells and Metastasis
- Keywords
- actin cytoskeleton, tumor cell dissemination, metastasis, tumor invasion, cell motility, metastatic colonization, actin dynamics
- MeSH terms
- Actins, Animals, Cell Cycle, Cell Movement, Humans, Neoplasm Metastasis, Neoplasms, Epithelial-Mesenchymal Transition
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