The Akt kinases Isoform specificity in metabolism and cancer

被引:483
作者
Gonzalez, Eva [1 ]
McGraw, Timothy E. [1 ]
机构
[1] Weill Cornell Med Coll, Dept Biochem, New York, NY 10065 USA
关键词
Akt; isoforms; metabolism; cancer; glucose homeostasis; GLUT4; signaling specificity; cellular growth; Akt1; Akt2; GTPASE-ACTIVATING-PROTEIN; STIMULATED GLUT4 TRANSLOCATION; MICE LACKING; GLUCOSE-HOMEOSTASIS; SKELETAL-MUSCLE; CELL-MIGRATION; GLUT4-CONTAINING VESICLES; INSULIN-RESISTANCE; SIGNALING PATHWAY; PLASMA-MEMBRANE;
D O I
10.4161/cc.8.16.9335
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
The Akt (PKB) protein kinases are critical regulators of human physiology that control an impressive array of diverse cellular functions, including the modulation of growth, survival, proliferation and metabolism. The Akt kinase family is comprised of three highly homologous isoforms: Akt1 (PKB alpha), Akt2 (PKB beta) and Akt3 (PKB gamma). Phenotypic analyses of Akt isoform knockout mice documented Akt isoform specific functions in the regulation of cellular growth, glucose homeostasis and neuronal development. Those studies establish that the functions of the different Akt kinases are not completely overlapping and that isoform-specific signaling contributes to the diversity of Akt activities. However, despite these important advances, a thorough understanding about the specific roles of Akt family members and the molecular mechanisms that determine Akt isoform functional specificity will be essential to elucidate the complexity of Akt regulated cellular processes and how Akt isoform-specific deregulation might contribute to disease states. Here, we summarize recent advances in understanding the roles of Akt isoforms in the regulation of metabolism and cancer, and possible mechanisms contributing to Akt isoform functional specificity.
引用
收藏
页码:2502 / 2508
页数:7
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