Diverse Mechanisms of AKT Pathway Activation in Human Malignancy

被引:175
作者
Cheung, Mitchell [1 ]
Testa, Joseph R. [1 ]
机构
[1] Fox Chase Canc Ctr, Canc Biol Program, Philadelphia, PA 19111 USA
关键词
AKT/PKB kinases; hemimegalencephaly; human malignancy; hypoglycemia; oncogenes; proteus syndrome; targeted therapies; tumor suppressor genes; PEUTZ-JEGHERS-SYNDROME; PLECKSTRIN HOMOLOGY DOMAIN; HUMAN PANCREATIC-CANCER; OVARIAN-CANCER; PROTEUS SYNDROME; PROSTATE-CANCER; CELL CARCINOMA; MOUSE MODEL; PIK3CA AMPLIFICATION; TUBEROUS SCLEROSIS;
D O I
10.2174/1568009611313030002
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
AKT/PKB (Protein Kinase B) are central proteins mediating signals from receptor tyrosine kinases and phosphatidylinositol 3-kinase. AKT kinases are involved in a number of important cellular processes including cell proliferation and survival, cell size in response to nutrient availability, tumor invasion/metastasis, and angiogenesis. Various components of the AKT signaling pathway are encoded by tumor suppressor genes and oncogenes whose loss or activation, respectively, plays an important role in tumorigenesis. The growing body of evidence connecting deregulated AKT signaling with sporadic human cancers and inherited cancer predisposition syndromes is discussed. We also highlight new findings regarding the involvement of activating mutations of AKT1, AKT2, and AKT3 in somatic overgrowth disorders: Proteus syndrome, hypoglycemia with hypertrophy, and hemimegalencephaly, respectively. In addition, we review recent literature documenting the various ways the AKT signaling pathway is activated in human cancers and consequences for molecularly targeted therapies.
引用
收藏
页码:234 / 244
页数:11
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