The phosphatidylinositol 3' –kinase (PI3K)-Akt signaling pathway is an intracellular signaling pathway important in regulating the cell cycle and is activated by many types of cellular stimuli or toxic insults.
It regulates fundamental cellular functions such as transcription, translation, proliferation, growth, and survival in response to extracellular signals. This is mediated through serine and/or threonine phosphorylation of a range of downstream substrates.
As shown in following picture, activation of growth factor receptor protein tyrosine kinases including epidermal growth factor receptor (EGFR) by external growth factors results in auto-phosphorylation on tyrosine residues and subsequent events to activate these intracellular pathways.
PI3K is recruited to the membrane by directly binding to phosphotyrosine consensus residues of growth factor receptors or adaptors through one or both SH2 domains in the adaptor subunit. This leads to allosteric activation of the catalytic subunit. Activation results in production of the second messenger phosphatidylinositol-3, 4, 5-trisphosphate (PIP3).
The lipid product of PI3K, PIP3, recruits a subset of signaling proteins with pleckstrin homology (PH) domains to the membrane, including PDK1 and Akt. PTEN, is a PI-3, 4, 5-P3 phosphatase, which negatively regulates the PI3K/Akt pathway.
Once activated, Akt mediates the activation and inhibition of several targets, resulting in cellular survival, growth and proliferation through various mechanisms. In the mechanism of PI3K-Akt signaling pathway, the key molecules involved in this signaling pathway are receptor tyrosine kinase (RTKs), phosphatidylinositol 3-kinase (PI3K), phosphatidylinositol-4,5-bisphosphate (PIP2), phosphatidylinositol-3,4,5-bisphosphate (PIP3) and AKT/protein kinase B.
Most genetic alterations associated with tumor phenotype are representative of a finite succession of physiologic disturbances, which, collectively, render the cell to become malignant. Alterations of the PI3K-Akt signaling pathway have been reported in numerous human cancers. The PI3K-Akt signaling pathway plays an important role in the characteristic process of cancer. For example, Akt overexpression or activation may lead to an increased response to ambient levels of growth factors. Sustained activation of Akt makes tumor cells insensitive to anti-proliferative signals by inducing nuclear entry of Mdm2, which leads to inhibition of p53 regulated processes and by inducing cytoplasmic localization of p21Cip/Waf1 and p27Kip, which promotes proliferation. Akt activation also suppresses apoptosis of cancer cells by inactivating pro-apoptotic factors Bad and pro-caspase-9, but by activating IKK that provokes the transcription of NF-κB regulated antiapoptotic genes. Besides, the PI3K-Akt pathway also promotes tumor angiogenesis through eNOS activation and contributes to invasiveness by inhibiting anoikis and stimulating MMP secretion.
There are numerous aberrant mutations of the PI3K-Akt pathway in human cancers, including loss of the lipid phosphatases PTEN and INPP4B, as well as mutation and amplification of the genes encoding the PI3K catalytic subunits p110α (PIK3CA) and p110β (PIK3CB), and so on. In recent clinic cancer treatment, several drugs targeting the PI3K-Akt pathway have been developed and are currently in clinical trials in different phases of clinical development, such as PI3K Inhibitors, Isoform-Specific PI3K Inhibitors, Dual PI3K/mTOR Inhibitors. However, these drugs are just observed early signals of clinical activity. A better understanding of this essential crossroad between PI3K-Akt signaling and cancer is conducive to fully exploit the potential benefits of these new drugs.
Under normal conditions, insulin is immediately secreted after a meal. The released insulin binds to and activates IRS-1/2 (insulin receptor substrate-1/2), initiating the PI3K-Akt signaling pathway. Insulin-mediated Akt pathway accelerates glucose utilization, reduces gluconeogenesis of liver and muscle, increases body lipid deposition, thereby reducing free fatty acid (FFA) circulation in adipose tissue, increases pancreatic insulin secretion, and regulates lipid and glucose metabolism balance, reduce brain appetite. However, in the case of chronic energy excessive conditions, such as obesity, lipid accumulation is saturated, resulting in increased lipolysis of adipose tissue, leading to excessive FFAs. Lipid ectopic accumulation of skeletal muscle leads to reduced glucose transport and glycogen synthesis. Excess FAAs also disrupts β-cell function and insulin secretion. In the liver, excess FAAs suppress extrahepatic insulin signal transduction and ectopic accumulation of lipids, leading to an increase in HGP (hepatic glucose production) and DNL (de novo lipogenesis). In the brain, excessive FFAs cause glucose and lipid metabolism disorders. All these eventually impairs the PI3K-Akt signal, inducing insulin resistance. Insulin resistance further exacerbates the PI3K-AKT signal, forming a vicious circle that leads to obesity and Type II diabetes. As the PI3K-Akt pathway is closely related to metabolism, regulation of PI3K-Akt signaling pathway and its downstream molecules is a potential therapeutic target for the treatment of obesity and type 2 diabetes.
|CSF1R||CSF1R Antibody||CSF1R Protein||CSF1R cDNA||CSF1R ELISA Kit|
|CSF3||CSF3 Antibody||CSF3 Protein||CSF3 cDNA||CSF3 ELISA Kit|
|CSF3R||CSF3R Antibody||CSF3R Protein||CSF3R cDNA||CSF3R ELISA Kit|
|CSH1||CSH1 Antibody||CSH1 Protein||CSH1 cDNA||CSH1 ELISA Kit|
|DDIT4||DDIT4 Antibody||DDIT4 Protein||DDIT4 cDNA||DDIT4 ELISA Kit|
|EFNA1||EFNA1 Antibody||EFNA1 Protein||EFNA1 cDNA||EFNA1 ELISA Kit|
|EFNA2||EFNA2 Antibody||EFNA2 Protein||EFNA2 cDNA||EFNA2 ELISA Kit|
|EFNA3||EFNA3 Antibody||EFNA3 Protein||EFNA3 cDNA||EFNA3 ELISA Kit|
|EFNA4||EFNA4 Antibody||EFNA4 Protein||EFNA4 cDNA||EFNA4 ELISA Kit|
|EFNA5||EFNA5 Antibody||EFNA5 Protein||EFNA5 cDNA||EFNA5 ELISA Kit|
|EGF||EGF Antibody||EGF Protein||EGF cDNA||EGF ELISA Kit|
|EGFR||EGFR Antibody||EGFR Protein||EGFR cDNA||EGFR ELISA Kit|
|EIF4B||EIF4B Antibody||EIF4B Protein||EIF4B cDNA||EIF4B ELISA Kit|
|EIF4E||EIF4E Antibody||EIF4E Protein||EIF4E cDNA||EIF4E ELISA Kit|
|EIF4E1B||EIF4E1B Antibody||EIF4E1B Protein||EIF4E1B cDNA||EIF4E1B ELISA Kit|
|EIF4E2||EIF4E2 Antibody||EIF4E2 Protein||EIF4E2 cDNA||EIF4E2 ELISA Kit|
|EIF4EBP1||EIF4EBP1 Antibody||EIF4EBP1 Protein||EIF4EBP1 cDNA||EIF4EBP1 ELISA Kit|
|EPHA2||EPHA2 Antibody||EPHA2 Protein||EPHA2 cDNA||EPHA2 ELISA Kit|
|EPO||EPO Antibody||EPO Protein||EPO cDNA||EPO ELISA Kit|
|EPOR||EPOR Antibody||EPOR Protein||EPOR cDNA||EPOR ELISA Kit|