Xie George, Okuda Sho, Gao Jing-Yan, Wu Timothy, Jeong Jessica, Lu Kun Ping, Zhou Xiao Zhen
Departments of Biochemistry and Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada.
Departments of Biochemistry and Oncology, Schulich School of Medicine & Dentistry, Western University, London, ON N6A 5C1, Canada; Department of Chemistry, Western University, London, ON N6A 5C1, Canada.
Semin Cancer Biol. 2025 Sep;114:173-194. doi: 10.1016/j.semcancer.2025.05.011. Epub 2025 May 22.
The prolyl-isomerase Pin1 is a unique enzyme that catalyzes cis-trans isomerization of phosphorylated Ser/Thr-Pro motifs. These motifs are present in many proteins, where isomerization of the typically rigid prolyl-peptide bond can lead to conformational changes, and subsequently regulate activity, stability, or localization. The specificity of Pin1 for phosphorylated motifs allows it to serve as a master regulator of proteins after phosphorylation, adding an additional layer of regulation to intricately control cellular signaling. As such, Pin1 plays an expansive role in numerous cancer and age-related signaling pathways, and is recognized as a major driver of cancer and promising therapeutic target. In this review, we discuss the role of Pin1 in regulation of age-related cancer signaling pathways, and we highlight the early development and current landscape of Pin1 inhibitors, and the prospect of Pin1 inhibition for cancer therapy.
脯氨酰异构酶Pin1是一种独特的酶,可催化磷酸化的丝氨酸/苏氨酸-脯氨酸基序的顺反异构化。这些基序存在于许多蛋白质中,其中典型的刚性脯氨酰肽键的异构化可导致构象变化,进而调节活性、稳定性或定位。Pin1对磷酸化基序的特异性使其能够在磷酸化后作为蛋白质的主要调节因子,为复杂地控制细胞信号传导增加了一层额外的调节。因此,Pin1在众多癌症和与年龄相关的信号通路中发挥着广泛作用,被认为是癌症的主要驱动因素和有前景的治疗靶点。在本综述中,我们讨论了Pin1在调节与年龄相关的癌症信号通路中的作用,并重点介绍了Pin1抑制剂的早期开发和当前情况,以及Pin1抑制用于癌症治疗的前景。