Signalling downstream of PI3 kinase in mammary epithelium: a play in 3 Akts

被引:74
作者
Wickenden, Julie A. [1 ]
Watson, Christine J. [1 ]
机构
[1] Univ Cambridge, Dept Pathol, Cambridge CB2 QP, England
来源
BREAST CANCER RESEARCH | 2010年 / 12卷 / 02期
基金
英国医学研究理事会;
关键词
NF-KAPPA-B; CANCER-CELL MOTILITY; PHOSPHATIDYLINOSITOL; 3-KINASE; DISTINCT ROLES; PHOSPHOINOSITIDE; TUMOR PROGRESSION; GLAND INVOLUTION; TRANSGENIC MICE; ACTIVATED AKT; MOUSE MODEL;
D O I
10.1186/bcr2558
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The protein serine/threonine kinase Akt, also known as protein kinase B (PKB), is arguably the most important signalling nexus in the cell. Akt integrates a plethora of extracellular signals to generate diverse outcomes, including proliferation, motility, growth, glucose homeostasis, survival, and cell death. The phosphatidylinositol 3-kinase (PI3K)/Akt pathway is the second most frequently mutated pathway in cancer, after p53, and mutations in components of this pathway are found in around 70% of breast cancers. Thus, understanding how Akt relays input signals to downstream effectors is critically important for the design of therapeutic strategies to combat breast cancer. In this review, we will discuss the various signals upstream of Akt that impact on its activity, how Akt integrates these signals and modulates the activity of downstream targets to control mammary gland development, and how mutations in components of the pathway result in breast cancer.
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页数:9
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