An updated review of small-molecule HPK1 kinase inhibitors (2016-present)

被引:2
作者
Duan, Yiping [1 ]
Guo, Zhichao [1 ]
Zhong, Wenyi [2 ]
Chen, Jichao [3 ]
Xu, Shengtao [1 ]
Liu, Jie [2 ]
Xu, Jinyi [1 ]
机构
[1] China Pharmaceut Univ, Sch Pharm, Dept Med Chem, Nanjing 211198, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, Sch Sci, Dept Organ Chem, Nanjing 211198, Jiangsu, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Pharm, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
anti-tumor; HPK1; inhibitor; immunotherapy; small-molecule inhibitors; T cell exhaustion; HEMATOPOIETIC PROGENITOR KINASE; NF-KAPPA-B; CANCER; IMMUNOTHERAPY; COMBINATION; BINDING; FAMILY; CELLS; MICROENVIRONMENT; PHOSPHORYLATION;
D O I
10.1080/17568919.2024.2420630
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hematopoietic progenitor kinase 1 (HPK1) is a serine-threonine kinase specific to hematopoiesis and a member of the MAP4K family of Ste20-related protein kinases. Targeting HPK1 to ameliorate T cell exhaustion and enhance T cell functions is a promising strategy for clinical immunotherapies. Numerous studies have reported the progress in developing effective HPK1 inhibitors and elucidating their mechanisms of action. However, most inhibitors affect multiple signaling pathways, resulting in unintended side effects that limit their clinical development and application. Herein, we reviewed HPK1-related signaling pathways, clinical candidates and recent advances in small-molecule inhibitors targeting HPK1. Additionally, we present our perspectives on current challenges and potential future research field, hoping to provide inspiration for the development of novel HPK1 inhibitors.
引用
收藏
页码:2431 / 2450
页数:20
相关论文
共 111 条
[1]   Endogenous Glucocorticoid Signaling Regulates CD8+T Cell Differentiation and Development of Dysfunction in the Tumor Microenvironment [J].
Acharya, Nandini ;
Madi, Asaf ;
Zhang, Huiyuan ;
Klapholz, Max ;
Escobar, Giulia ;
Dulberg, Shai ;
Christian, Elena ;
Ferreira, Michelle ;
Dixon, Karen O. ;
Fell, Geoffrey ;
Tooley, Katherine ;
Mangani, Davide ;
Xia, Junrong ;
Singer, Meromit ;
Bosenberg, Marcus ;
Neuberg, Donna ;
Rozenblatt-Rosen, Orit ;
Regev, Aviv ;
Kuchroo, Vijay K. ;
Anderson, Ana C. .
IMMUNITY, 2020, 53 (03) :658-+
[2]   Axitinib for the treatment of advanced renal cell carcinoma [J].
Akaza, Hideyuki ;
Fukuyama, Tomofusa .
EXPERT OPINION ON PHARMACOTHERAPY, 2014, 15 (02) :283-297
[3]   Hematopoietic progenitor kinase 1 is a critical component of prostaglandin E2-mediated suppression of the anti-tumor immune response [J].
Alzabin, Saba ;
Pyarajan, Saiju ;
Yee, Herman ;
Kiefer, Friedemann ;
Suzuki, Akira ;
Burakoff, Steven ;
Sawasdikosol, Sansana .
CANCER IMMUNOLOGY IMMUNOTHERAPY, 2010, 59 (03) :419-429
[4]   Hematopoietic Progenitor Kinase 1 Is a Negative Regulator of Dendritic Cell Activation [J].
Alzabin, Saba ;
Bhardwaj, Nina ;
Kiefer, Friedemann ;
Sawasdikosol, Sansana ;
Burakoff, Steven .
JOURNAL OF IMMUNOLOGY, 2009, 182 (10) :6187-6194
[5]   Small-molecule PROTACs: An emerging and promising approach for the development of targeted therapy drugs [J].
An, Sainan ;
Fu, Liwu .
EBIOMEDICINE, 2018, 36 :553-562
[6]  
[Anonymous], 2019, Patent No. [WO2019206049Al, 2019206049]
[7]  
[Anonymous], 2020, Patent No. [CN112552293A, 112552293]
[8]  
[Anonymous], 2020, Patent No. [WO2020193512Al, 2020193512]
[9]  
[Anonymous], Safety and Efficacy Study of TAK-700 in Patients With Nonmetastatic Castration-resistant Prostate Cancer and a Rising Prostate-specific Antigen
[10]  
[Anonymous], STUDY NDI 1150 101 P