A portrait of AKT kinases - Human cancer and animal models depict a family with strong individualities

被引:109
作者
Bellacosa, A
Testa, JR
Moore, R
Larue, L
机构
[1] Fox Chase Canc Ctr, Human Genet Program, Philadelphia, PA 19111 USA
[2] Dev Genet Melanocytes Inst Curie, Orsay, France
关键词
AKT/PKB kinases; oncogenes; tumor suppressor genes; human cancer; animal models;
D O I
10.4161/cbt.3.3.703
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
More than a decade after their discovery, the three AKT kinase family members have emerged as central players in the signaling cascades that regulate cell growth, proliferation, survival and various aspects of intermediary metabolism. The mechanisms of activation of AKT kinases have been defined in relatively precise terms and new substrates are currently being validated in vivo. However, it is presently unclear whether AKT1, AKT2 and AKT3 are functionally redundant or whether each one performs specific functional role(s). In this review, we will summarize the signaling properties and highlight the specificities of AKT kinases that have emerged from the study of human cancer and animal models. While AKT kinases are an attractive target for pharmacological intervention, knowledge of the precise individual roles of AKT family members will improve the design of highly specific AKT-based therapeutics having reduced toxicity and improved efficacy.
引用
收藏
页码:268 / 275
页数:8
相关论文
共 118 条
[1]   Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha [J].
Alessi, DR ;
James, SR ;
Downes, CP ;
Holmes, AB ;
Gaffney, PRJ ;
Reese, CB ;
Cohen, P .
CURRENT BIOLOGY, 1997, 7 (04) :261-269
[2]   Frequent activation of AKT2 kinase in human pancreatic carcinomas (vol 87, pg 470, 2002) [J].
Altomare, DA ;
Tanno, S ;
De Rienzo, A ;
Klein-Szanto, A ;
Tanno, S ;
Skele, KL ;
Hoffman, JP ;
Testa, JR .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2003, 88 (01) :470-476
[3]   Colonic polyposis caused by mTOR-mediated chromosomal instability in Apc+/Δ716 Cdx2+/- compound mutant mice [J].
Aoki, K ;
Tamai, Y ;
Horiike, S ;
Oshima, M ;
Taketo, MM .
NATURE GENETICS, 2003, 35 (04) :323-330
[4]  
Arboleda MJ, 2003, CANCER RES, V63, P196
[5]   AKT2 is frequently upregulated in HER-2/neu-positive breast cancers and may contribute to tumor aggressiveness by enhancing cell survival [J].
Bacus, SS ;
Altomare, DA ;
Lyass, L ;
Chin, DM ;
Farrell, MP ;
Gurova, K ;
Gudkov, A ;
Testa, JR .
ONCOGENE, 2002, 21 (22) :3532-3540
[6]   Akt activation by growth factors is a multiple-step process: the role of the PH domain [J].
Bellacosa, A ;
Chan, TO ;
Ahmed, NN ;
Datta, K ;
Malstrom, S ;
Stokoe, D ;
McCormick, F ;
Feng, JN ;
Tsichlis, P .
ONCOGENE, 1998, 17 (03) :313-325
[7]   MOLECULAR ALTERATIONS OF THE AKT2 ONCOGENE IN OVARIAN AND BREAST CARCINOMAS [J].
BELLACOSA, A ;
DEFEO, D ;
GODWIN, AK ;
BELL, DW ;
CHENG, JQ ;
ALTOMARE, DA ;
WAN, MH ;
DUBEAU, L ;
SCAMBIA, G ;
MASCIULLO, V ;
FERRANDINA, G ;
PANICI, PB ;
MANCUSO, S ;
NERI, G ;
TESTA, JR .
INTERNATIONAL JOURNAL OF CANCER, 1995, 64 (04) :280-285
[8]   A RETROVIRAL ONCOGENE, AKT, ENCODING A SERINE-THREONINE KINASE CONTAINING AN SH2-LIKE REGION [J].
BELLACOSA, A ;
TESTA, JR ;
STAAL, SP ;
TSICHLIS, PN .
SCIENCE, 1991, 254 (5029) :274-277
[9]   Islet β cell expression of constitutively active Akt1/PKBα induces striking hypertrophy, hyperplasia, and hyperinsulinemia [J].
Bernal-Mizrachi, E ;
Wen, W ;
Stahlhut, S ;
Welling, CM ;
Permutt, MA .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (11) :1631-1638
[10]   Frequent monoallelic deletion of PTEN and its reciprocal associatioin with PIk3CA amplification in gastric carcinoma [J].
Byun, DS ;
Cho, K ;
Ryu, BK ;
Lee, MG ;
Park, JI ;
Chae, KS ;
Kim, HJ ;
Chi, SG .
INTERNATIONAL JOURNAL OF CANCER, 2003, 104 (03) :318-327