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Pak protein kinases and their role in cancer
- Source :
- Cancer and Metastasis Reviews. 28:51-63
- Publication Year :
- 2009
- Publisher :
- Springer Science and Business Media LLC, 2009.
-
Abstract
- Some of the characteristics of cancer cells are high rates of cell proliferation, cell survival, and the ability to invade surrounding tissue. The cytoskeleton has an essential role in these processes. Dynamic changes in the cytoskeleton are necessary for cell motility and cancer cells are dependent on motility for invasion and metastasis. The signaling pathways behind the reshaping and migrating properties of the cytoskeleton in cancer cells involve a group of Ras-related small GTPases and their effectors, including the p21-activated kinases (Paks). Paks are a family of serine/threonine protein kinases comprised of six isoforms (Pak 1-6), all of which are direct targets of the small GTPases Rac and Cdc42. Besides their role in cytoskeletal dynamics, Paks have recently been shown to regulate various other cellular activities, including cell survival, mitosis, and transcription. Paks are overexpressed and/or hyperactivated in several human tumors and their role in cell transformation makes them attractive therapeutic targets. Pak-targeted therapeutics may efficiently inhibit certain types of tumors and efforts to identify selective Pak-inhibitors are underway.
- Subjects :
- Cancer Research
Apoptosis
macromolecular substances
CDC42
Biology
Article
Gene Expression Regulation, Enzymologic
Substrate Specificity
Neoplasms
Animals
Humans
cdc42 GTP-Binding Protein
Cytoskeleton
p21-activated kinases
Cell growth
Kinase
Protein Structure, Tertiary
rac GTP-Binding Proteins
Cell biology
Gene Expression Regulation, Neoplastic
Rac GTP-Binding Proteins
Cell Transformation, Neoplastic
p21-Activated Kinases
Oncology
Cdc42 GTP-Binding Protein
Cancer cell
Cancer research
Signal Transduction
Subjects
Details
- ISSN :
- 15737233 and 01677659
- Volume :
- 28
- Database :
- OpenAIRE
- Journal :
- Cancer and Metastasis Reviews
- Accession number :
- edsair.doi.dedup.....1d398f188ff5cc6fd81c89d41f7e2478
- Full Text :
- https://doi.org/10.1007/s10555-008-9168-1