2001
DOI: 10.1038/35077225
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Oncogenic kinase signalling

Abstract: Protein-tyrosine kinases (PTKs) are important regulators of intracellular signal-transduction pathways mediating development and multicellular communication in metazoans. Their activity is normally tightly controlled and regulated. Perturbation of PTK signalling by mutations and other genetic alterations results in deregulated kinase activity and malignant transformation. The lipid kinase phosphoinositide 3-OH kinase (PI(3)K) and some of its downstream targets, such as the protein-serine/threonine kinases Akt … Show more

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Cited by 3,374 publications
(2,517 citation statements)
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References 88 publications
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“…22 One of the intracellular signaling pathways that are frequently activated in cancer cells is the PI3K/Akt kinase pathway. 23 This pathway has been documented as an important signaling for cell survival, cell transformation and tumor growth. PI3K catalyzes the formation of the 3' phosphoinositides, phosphatidylinositol 3,4-diphosphate (PIP2) and phosphatidylinositol 3,4,5-triphosphate.…”
Section: Discussionmentioning
confidence: 99%
“…22 One of the intracellular signaling pathways that are frequently activated in cancer cells is the PI3K/Akt kinase pathway. 23 This pathway has been documented as an important signaling for cell survival, cell transformation and tumor growth. PI3K catalyzes the formation of the 3' phosphoinositides, phosphatidylinositol 3,4-diphosphate (PIP2) and phosphatidylinositol 3,4,5-triphosphate.…”
Section: Discussionmentioning
confidence: 99%
“…SFK are known oncogenes 47 and can be downregulated by Srcasm 48. Increased activation of SFK and decreased Srcasm levels were reported in CSCC compared with unremarkable epidermis 27, 49, 50.…”
Section: Notch Signaling In Cutaneous Squamous Cell Carcinoma (Cscc)mentioning
confidence: 99%
“…Through tyrosine phosphorylation, they mediate the activation of a number of downstream signaling proteins. 54 Ligand binding as well as cell-cell interactions through cell adhesion molecules activate these enzymes. 55 Phosphorylated tyrosine residues in specific domains of these receptors serve as high-affinity docking sites for SH2-containing adaptor and effector proteins.…”
Section: Constitutively Active Kinases As Targets Of Therapymentioning
confidence: 99%