Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11591
Title: p21-activated kinases and gastrointestinal cancer.
Authors: He, Hong;Baldwin, Graham S
Affiliation: Department of Surgery, University of Melbourne, Austin Health, Melbourne, Victoria, Australia.
Issue Date: 22-Oct-2012
Citation: Biochimica Et Biophysica Acta 2012; 1833(1): 33-9
Abstract: p21-activated kinases (PAKs) were initially identified as effector proteins downstream from GTPases of the Rho family. To date, six members of the PAK family have been discovered in mammalian cells. PAKs play important roles in growth factor signalling, cytoskeletal remodelling, gene transcription, cell proliferation and oncogenic transformation. A large body of research has demonstrated that PAKs are up-regulated in several human cancers, and that their overexpression is linked to tumour progression and resistance to therapy. Structural and biochemical studies have revealed the mechanisms involved in PAK signalling, and opened the way to the development of PAK-targeted therapies for cancer treatment. Here we summarise recent findings from biological and clinical research on the role of PAKs in gastrointestinal cancer, and discuss the current status of PAK-targeted anticancer therapies.
Internal ID Number: 23092728
URI: http://ahro.austin.org.au/austinjspui/handle/1/11591
DOI: 10.1016/j.bbamcr.2012.10.015
URL: http://www.ncbi.nlm.nih.gov/pubmed/23092728
Type: Journal Article
Subjects: Animals
Carcinoma.genetics.metabolism
Gastrointestinal Neoplasms.genetics.metabolism
Humans
Models, Biological
Molecular Targeted Therapy.methods.trends
p21-Activated Kinases.chemistry.genetics.metabolism.physiology
Appears in Collections:Journal articles

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