Kawano Takahito, Inokuchi Junichi, Eto Masatoshi, Murata Masaharu, Kang Jeong-Hun
Center for Advanced Medical Innovation, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Department of Urology, Graduate School of Medical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan.
Pharmaceutics. 2021 Oct 20;13(11):1748. doi: 10.3390/pharmaceutics13111748.
Protein kinase C (PKC), a family of phospholipid-dependent serine/threonine kinase, is classed into three subfamilies based on their structural and activation characteristics: conventional or classic PKC isozymes (cPKCs; α, βI, βII, and γ), novel or non-classic PKC isozymes (nPKCs; δ, ε, η, and θ), and atypical PKC isozymes (aPKCs; ζ, ι, and λ). PKC inhibitors and activators are used to understand PKC-mediated intracellular signaling pathways and for the diagnosis and treatment of various PKC-associated diseases, such as cancers, neurological diseases, cardiovascular diseases, and infections. Many clinical trials of PKC inhibitors in cancers showed no significant clinical benefits, meaning that there is a limitation to design a cancer therapeutic strategy targeting PKC alone. This review will focus on the activators and inhibitors of PKC and their applications in clinical trials.
蛋白激酶C(PKC)是一类磷脂依赖性丝氨酸/苏氨酸激酶,根据其结构和激活特性分为三个亚家族:传统或经典PKC同工酶(cPKC;α、βI、βII和γ)、新型或非经典PKC同工酶(nPKC;δ、ε、η和θ)以及非典型PKC同工酶(aPKC;ζ、ι和λ)。PKC抑制剂和激活剂用于了解PKC介导的细胞内信号通路,以及诊断和治疗各种与PKC相关的疾病,如癌症、神经疾病、心血管疾病和感染。许多PKC抑制剂在癌症中的临床试验显示没有显著的临床益处,这意味着仅针对PKC设计癌症治疗策略存在局限性。本综述将聚焦于PKC的激活剂和抑制剂及其在临床试验中的应用。