PDK1: At the crossroad of cancer signaling pathways

被引:153
作者
Gagliardi, Paolo Armando [1 ]
Puliafito, Alberto [1 ]
Primo, Luca [1 ,2 ]
机构
[1] Candiolo Canc Inst FPO IRCCS, Str Prov 142 KM 3-95, I-10060 Candiolo, Italy
[2] Univ Torino, Dept Oncol, Turin, Italy
关键词
PDPK1; PI3K/Akt; Ras/MAPK; Myc; Tumor microenvironment; 3-PHOSPHOINOSITIDE-DEPENDENT PROTEIN KINASE-1; PLECKSTRIN HOMOLOGY DOMAIN; NF-KAPPA-B; CELL-MIGRATION; C-MYC; PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE; TUMOR MICROENVIRONMENT; TARGETED THERAPY; PROSTATE-CANCER; MTOR COMPLEX;
D O I
10.1016/j.semcancer.2017.04.014
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rational target therapy of cancer would benefit from the identification of new targets that can be easily inhibited by small molecules. An increasing amount of evidence hints at 3-phosphoinositide dependent protein kinase-1 (PDK1 or PDPK1) as an intriguing and underexplored target for cancer therapy. Several reports show that PDK1 expression is dysregulated in multiple cancer types. Furthermore PDK1 is implicated in signaling pathways frequently altered in cancer, such as PI3K/Akt, Ras/MAPK and Myc. PDK1 targeting has been proven to be effective in experimental models harboring alterations of these pathways. In this paper we review PDK1 main biochemical mechanisms, its alterations in cancer and interactions with relevant cancer pathways. A potential role of PDK1 in tumor microenvironment is also discussed.
引用
收藏
页码:27 / 35
页数:9
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