Comprehensive Pneumology Center (CPC), Helmholtz Center Munich, Max-Lebsche Platz 31, 81377 Munich, Germany.
Institut für Medizinische Biochemie und Molekularbiologie (IMBM), Universitätsmedizin Greifswald, Ferdinand-Sauerbruch-Straße, Klinikum DZ/7, 17475 Greifswald, Germany.
Biomolecules. 2022 Aug 20;12(8):1150. doi: 10.3390/biom12081150.
Proteasomes comprise a family of proteasomal complexes essential for maintaining protein homeostasis. Accordingly, proteasomes represent promising therapeutic targets in multiple human diseases. Several proteasome inhibitors are approved for treating hematological cancers. However, their side effects impede their efficacy and broader therapeutic applications. Therefore, understanding the biology of the different proteasome complexes present in the cell is crucial for developing tailor-made inhibitors against specific proteasome complexes. Here, we will discuss the structure, biology, and function of the alternative Proteasome Activator 200 (PA200), also known as PSME4, and summarize the current evidence for its dysregulation in different human diseases. We hereby aim to stimulate research on this enigmatic proteasome regulator that has the potential to serve as a therapeutic target in cancer.
蛋白酶体由一系列蛋白酶体复合物组成,对于维持蛋白质的内稳态至关重要。因此,蛋白酶体是多种人类疾病中很有前途的治疗靶点。几种蛋白酶体抑制剂已被批准用于治疗血液系统癌症。然而,它们的副作用阻碍了它们的疗效和更广泛的治疗应用。因此,了解细胞中存在的不同蛋白酶体复合物的生物学特性对于开发针对特定蛋白酶体复合物的定制抑制剂至关重要。在这里,我们将讨论替代蛋白酶体激活剂 200(PA200),也称为 PSME4 的结构、生物学和功能,并总结其在不同人类疾病中失调的现有证据。我们旨在激发对这种神秘的蛋白酶体调节剂的研究,它有可能成为癌症的治疗靶点。