Distinct Biological Roles for the Akt Family in Mammary Tumor Progression

被引:125
作者
Dillon, Rachelle L. [4 ]
Muller, William J. [1 ,2 ,3 ]
机构
[1] McGill Univ, Goodman Canc Ctr, Montreal, PQ H3G 0B1, Canada
[2] McGill Univ, Dept Biochem, Montreal, PQ H3G 0B1, Canada
[3] McGill Univ, Dept Med, Montreal, PQ H3G 0B1, Canada
[4] Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB, Canada
基金
加拿大健康研究院; 美国国家卫生研究院;
关键词
PROTEIN-KINASE-B/AKT; BREAST-CANCER; CELL-MIGRATION; INVASION; ACTIVATION; MOTILITY; ISOFORMS; POSH;
D O I
10.1158/0008-5472.CAN-10-0266
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The phosphatidylinositol 3' kinase/Akt pathway is frequently dysregulated in cancer, which can have unfavorable consequences in terms of cell proliferation, survival, metabolism, and migration. Increasing evidence suggests that Akt1, Akt2, and Akt3 play unique roles in breast cancer initiation and progression. We have recently shown that in contrast to Akt1, which accelerates mammary tumor induction in transgenic mice, Akt2 promotes metastasis of tumor cells without affecting the latency of tumor development. Despite the distinct phenotypic outputs resulting from Akt1 or Akt2 activation, very little is known about the mode by which such unique functions originate from these highly related kinases. Here we discuss potential mechanisms contributing to the differing functional specificity of Akt1 and Akt2 with respect to migration, invasion, and metastasis. Cancer Res; 70(11); 4260-4. (C) 2010 AACR.
引用
收藏
页码:4260 / 4264
页数:5
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