The PTEN-AKT3 signaling cascade as a therapeutic target in melanoma

被引:113
作者
Madhunapantula, SubbaRao V. [1 ]
Robertson, Gavin P. [1 ,2 ,3 ]
机构
[1] Penn State Univ, Coll Med, Dept Pharmacol, Hershey, PA 17033 USA
[2] Penn State Univ, Penn State Canc Inst,Coll Med, Foreman Fdn Melanoma Res,Dept Pathol, Penn State Melanoma Therapeut Program, Hershey, PA USA
[3] Penn State Univ, Penn State Canc Inst,Coll Med, Foreman Fdn Melanoma Res,Dept Dermatol, Penn State Melanoma Therapeut Program, Hershey, PA USA
关键词
melanoma; Akt3; PTEN; oncogene; tumorigenesis; apoptosis; PROTEIN-KINASE-B; PTEN TUMOR-SUPPRESSOR; RICH AKT-SUBSTRATE; PLECKSTRIN HOMOLOGY DOMAIN; GLYCOGEN-SYNTHASE KINASE; CELL-SURVIVAL; KAPPA-B; PROMOTER METHYLATION; PHOSPHATASE-ACTIVITY; MALIGNANT-MELANOMA;
D O I
10.1111/j.1755-148X.2009.00585.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
P>Melanocytes undergo extensive genetic changes during transformation into aggressive melanomas. These changes deregulate genes whose aberrant activity promotes the development of this disease. The phosphoinositide-3-kinase (PI3K) and mitogen-activated protein (MAP) kinase pathways are two key signaling cascades that have been found to play prominent roles in melanoma development. These pathways relay extra-cellular signals via an ordered series of consecutive phosphorylation events from cell surface throughout the cytoplasm and nucleus regulating diverse cellular processes including proliferation, survival, invasion and angiogenesis. It is generally accepted that therapeutic agents would need to target these two pathways to be an effective therapy for the long-term treatment of advanced-stage melanoma patients. This review provides an overview of the PI3 kinase pathway focusing specifically on two members of the pathway, called PTEN and Akt3, which play important roles in melanoma development. Mechanisms leading to deregulation of these two proteins and therapeutic implications of targeting this signaling cascade to treat melanoma are detailed in this review.
引用
收藏
页码:400 / 419
页数:20
相关论文
共 187 条
[41]   Hexamethylene bisacetamide (HMBA) simultaneously targets AKT and MAPK pathway and represses NFκB activity Implications for cancer therapy [J].
Dey, Anwesha ;
Wong, Eetsin ;
Kua, Nelly ;
Teo, Hsiang Ling ;
Tergaonkar, Vinay ;
Lane, David .
CELL CYCLE, 2008, 7 (23) :3759-3767
[42]  
Dhawan P, 2002, CANCER RES, V62, P7335
[43]   Pten is essential for embryonic development and tumour suppression [J].
Di Cristofano, A ;
Pesce, B ;
Cordon-Cardo, C ;
Pandolfi, PP .
NATURE GENETICS, 1998, 19 (04) :348-355
[44]  
Dufner A, 1999, MOL CELL BIOL, V19, P4525
[45]   Protein kinase B/Akt at a glance [J].
Fayard, E ;
Tintignac, LA ;
Baudry, A ;
Hemmings, BA .
JOURNAL OF CELL SCIENCE, 2005, 118 (24) :5675-5678
[46]   Active-Site Inhibitors of mTOR Target Rapamycin-Resistant Outputs of mTORC1 and mTORC2 [J].
Feldman, Morris E. ;
Apsel, Beth ;
Uotila, Aino ;
Loewith, Robbie ;
Knight, Zachary A. ;
Ruggero, Davide ;
Shokat, Kevan M. .
PLOS BIOLOGY, 2009, 7 (02) :371-383
[47]   Structural basis for discrimination of 3-phosphoinositides by pleckstrin homology domains [J].
Ferguson, KM ;
Kavran, JM ;
Sankaran, VG ;
Fournier, E ;
Isakoff, SJ ;
Skolnik, EY ;
Lemmon, MA .
MOLECULAR CELL, 2000, 6 (02) :373-384
[48]   Effect of phosphoinositide-dependent kinase 1 on protein kinase B translocation and its subsequent activation [J].
Filippa, N ;
Sable, CL ;
Hemmings, BA ;
Van Obberghen, E .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (15) :5712-5721
[49]   PRAS40 is a target for mammalian target of rapamycin complex 1 and is required for signaling downstream of this complex [J].
Fonseca, Bruno D. ;
Smith, Ewan M. ;
Lee, Vivian H. -Y. ;
MacKintosh, Carol ;
Proud, Christopher G. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (34) :24514-24524
[50]   THE PROTEIN-KINASE ENCODED BY THE AKT PROTOONCOGENE IS A TARGET OF THE PDGF-ACTIVATED PHOSPHATIDYLINOSITOL 3-KINASE [J].
FRANKE, TF ;
YANG, SI ;
CHAN, TO ;
DATTA, K ;
KAZLAUSKAS, A ;
MORRISON, DK ;
KAPLAN, DR ;
TSICHLIS, PN .
CELL, 1995, 81 (05) :727-736