Choosing Kinase Inhibitors for Androgen Deprivation Therapy-Resistant Prostate Cancer.
Pharmaceutics
; 14(3)2022 Feb 24.
Article
em En
| MEDLINE
| ID: mdl-35335873
Androgen deprivation therapy (ADT) is a systemic therapy for advanced prostate cancer (PCa). Although most patients initially respond to ADT, almost all cancers eventually develop castration resistance. Castration-resistant PCa (CRPC) is associated with a very poor prognosis, and the treatment of which is a serious clinical challenge. Accumulating evidence suggests that abnormal expression and activation of various kinases are associated with the emergence and maintenance of CRPC. Many efforts have been made to develop small molecule inhibitors to target the key kinases in CRPC. These inhibitors are designed to suppress the kinase activity or interrupt kinase-mediated signal pathways that are associated with PCa androgen-independent (AI) growth and CRPC development. In this review, we briefly summarize the roles of the kinases that are abnormally expressed and/or activated in CRPC and the recent advances in the development of small molecule inhibitors that target kinases for the treatment of CRPC.
AMP-activated protein kinase (AMPK); IκB kinase (IKK); LIM-domain kinase-2 (LIMK2); NEK6 (a mitotic-related serine/threonine kinase); PIM1 kinase; T-LAK cell-originated protein kinase (TOPK); TANK-binding kinase 1 (TBK1); androgen deprivation therapy (ADT); aurora kinase A (AURKA); bromodomain (BRD)-containing kinases (BETs); castration-resistant prostate cancer (CRPC); cyclin-dependent kinases (CDKs); glycogen-synthase-kinase 3ß (GSK-3ß); hexokinase; jun kinase (JNK); kinase; kinase inhibitors; mitogen-activated protein kinase (MAPK); phosphatidylinositol 4-phosphate 5-kinase type 1α (PIP5K1α); phosphatidylinositol-3-kinase (PI3K)/AKT; phosphofructokinase (PFK); polo-like kinase 1 (PLK1); protein kinase A (PKA); riboflavin kinases (RFK); sphingosine kinases (SKs); the non-receptor tyrosine kinases (NRTKs); the receptor tyrosine kinases (RTKs); thymidine kinase; tumor progression locus 2 (Tpl2)
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1
Coleções:
01-internacional
Base de dados:
MEDLINE
Idioma:
En
Revista:
Pharmaceutics
Ano de publicação:
2022
Tipo de documento:
Article
País de afiliação:
China