Università di Napoli Federico II, Facoltà di Farmacia, Dipartimento di Chimica Farmaceutica e Tossicologica, Drug Discovery Laboratory, Via D. Montesano 49, Napoli, 80131, Italy.
Expert Opin Ther Pat. 2010 Mar;20(3):405-25. doi: 10.1517/13543771003623232.
The cell division cycle 25 (Cdc25) family of proteins are highly conserved dual specificity phosphatases that regulate cyclin-dependent kinases, the main gatekeepers of the eukaryotic cell division cycle. The three isoforms of Cdc25, including Cdc25A, Cdc25B and Cdc25C, appear to act on different cyclin-dependent kinase/cyclin complexes at different stages of the cell cycle. Overexpression of Cdc25A and/or Cdc25B, but not Cdc25C, has been detected in numerous cancers and is often correlated with a poor clinical prognosis. Thus, inhibition of these phosphatases may represent a promising therapeutic approach in oncology.
The main focus of the present review is to describe the development of Cdc25 inhibitors over the years. We describe different compounds according to the decade of discovery and focus attention on molecules that were published in patents.
Insight into the most clinically relevant therapeutic Cdc25 analogues that have been published in over 40 patents over the past 19 years.
Some Cdc25 inhibitors have suppressed in vivo the growth of human tumor xenografts in animals; this confirmed the validity of using Cdc25 phosphatase inhibition as an anticancer strategy, but side effects and toxicity remain to be investigated.
细胞分裂周期 25(Cdc25)蛋白家族是高度保守的双特异性磷酸酶,可调节细胞周期蛋白依赖性激酶,这是真核细胞分裂周期的主要监管者。Cdc25 的三种同工型,包括 Cdc25A、Cdc25B 和 Cdc25C,似乎在细胞周期的不同阶段作用于不同的细胞周期蛋白依赖性激酶/细胞周期蛋白复合物。在许多癌症中检测到 Cdc25A 和/或 Cdc25B 的过表达,而不是 Cdc25C,并且通常与不良的临床预后相关。因此,抑制这些磷酸酶可能代表肿瘤学中一种有前途的治疗方法。
本综述的主要重点是描述多年来 Cdc25 抑制剂的发展。我们根据发现的十年描述了不同的化合物,并将注意力集中在已发表专利的分子上。
深入了解过去 19 年中在 40 多项专利中发表的最具临床相关性的治疗性 Cdc25 类似物。
一些 Cdc25 抑制剂已在动物中抑制了人肿瘤异种移植物的体内生长;这证实了使用 Cdc25 磷酸酶抑制作为抗癌策略的有效性,但仍需研究副作用和毒性。