Abstract:
: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.
journal_name
Cancer Resjournal_title
Cancer researchauthors
Dillon RL,Muller WJdoi
10.1158/0008-5472.CAN-10-0266subject
Has Abstractpub_date
2010-06-01 00:00:00pages
4260-4issue
11eissn
0008-5472issn
1538-7445pii
0008-5472.CAN-10-0266journal_volume
70pub_type
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