Master kinase PDK1 in tumorigenesis

被引:13
|
作者
Zheng, Nana [1 ,2 ]
Wei, Jiaqi [1 ,2 ]
Wu, Depei [1 ,2 ]
Xu, Yang [1 ,2 ]
Guo, Jianping [1 ,3 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, Jiangsu Inst Hematol, Natl Clin Res Ctr Hematol Dis, Suzhou 215006, Peoples R China
[2] Soochow Univ, Inst Blood & Marrow Transplantat, Collaborat Innovat Ctr Hematol, Suzhou 215006, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 1, Inst Precis Med, Guangzhou 510275, Guangdong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
PDK1; AGC kinase; Tumorigenesis; Tumor microenvironment; Target therapy; 3-PHOSPHOINOSITIDE-DEPENDENT PROTEIN KINASE-1; NF-KAPPA-B; IN-VIVO ROLE; TYROSINE PHOSPHORYLATION; TARGETING PDK1; CELL-SURVIVAL; CANCER-CELLS; NEGATIVE REGULATION; TUMOR PROGRESSION; PROSTATE-CANCER;
D O I
10.1016/j.bbcan.2023.188971
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
3-phosphoinositide-dependent protein kinase 1 (PDK1) is considered as master kinase regulating AGC kinase family members such as AKT, SGK, PLK, S6K and RSK. Although autophosphorylation regulates PDK1 activity, accumulating evidence suggests that PDK1 is manipulated by many other mechanisms, including S6K-mediated phosphorylation, and the E3 ligase SPOP-mediated ubiquitination and degradation. Dysregulation of these up-stream regulators or downstream signals involves in cancer development, as PDK1 regulating cell growth, metastasis, invasion, apoptosis and survival time. Meanwhile, overexpression of PDK1 is also exposed in a plethora of cancers, whereas inhibition of PDK1 reduces cell size and inhibits tumor growth and progression. More importantly, PDK1 also modulates the tumor microenvironments and markedly influences tumor immu-notherapies. In summary, we comprehensively summarize the downstream signals, upstream regulators, mouse models, inhibitors, tumor microenvironment and clinical treatments for PDK1, and highlight PDK1 as a potential cancer therapeutic target.
引用
收藏
页数:13
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