Elliott Peter J, Zollner Thomas Matthias, Boehncke Wolf-Henning
CombinatoRx Inc., Boston, Massachusetts, USA.
J Mol Med (Berl). 2003 Apr;81(4):235-45. doi: 10.1007/s00109-003-0422-2. Epub 2003 Mar 26.
The ubiquitin-proteasome pathway has a central role in the selective degradation of intracellular proteins. Among the key proteins modulated by the proteasome are those involved in the control of inflammatory processes, cell cycle regulation, and gene expression. Consequently proteasome inhibition is a potential treatment option for cancer and inflammatory conditions. Thus far, proof of principle has been obtained from studies in numerous animal models for a variety of human diseases including cancer, reperfusion injury, and inflammatory conditions such as rheumatoid arthritis, asthma, multiple sclerosis, and psoriasis. Two proteasome inhibitors, each representing a unique chemical class, are currently under clinical evaluation. Velcade (PS-341) is currently being evaluated in multiple phase II clinical trials for several solid tumor indications and has just entered a phase III trial for multiple myeloma. PS-519, representing another class of inhibitors, focuses on the inflammatory events following ischemia and reperfusion injury. Since proteasome inhibitors exhibit anti-inflammatory and antiproliferative effects, diseases characterized by both of these processes simultaneously, as is the case in rheumatoid arthritis or psoriasis, might also represent clinical opportunities for such drugs.
泛素-蛋白酶体途径在细胞内蛋白质的选择性降解中起核心作用。蛋白酶体调节的关键蛋白质包括那些参与炎症过程控制、细胞周期调节和基因表达的蛋白质。因此,蛋白酶体抑制是癌症和炎症性疾病的一种潜在治疗选择。到目前为止,在众多动物模型中针对包括癌症、再灌注损伤以及类风湿性关节炎、哮喘、多发性硬化症和牛皮癣等炎症性疾病在内的多种人类疾病的研究已获得原理验证。目前有两种蛋白酶体抑制剂,每种代表一种独特的化学类别,正在进行临床评估。万珂(PS-341)目前正在针对多种实体瘤适应症进行多项II期临床试验评估,并且刚刚进入针对多发性骨髓瘤的III期试验。代表另一类抑制剂的PS-519专注于缺血再灌注损伤后的炎症事件。由于蛋白酶体抑制剂具有抗炎和抗增殖作用,像类风湿性关节炎或牛皮癣那样同时以这两种过程为特征的疾病,可能也是这类药物的临床应用机会。