摘要
背景:Eph受体在发育过程和疾病中发挥重要功能,其中EphA2因其在癌症中的有争议的作用而众所周知。药物发现策略主要集中在EphA2胞外配体结合结构域,然而,受体还包含在C末端的大部分未开发的胞质Sam(无菌α基序)结构域。 EphA2-Sam结合来自脂质磷酸酶Ship2和Odin的第一个Sam结构域的Sam结构域。 Sam-Sam相互作用对于调节配体诱导的受体内吞作用和降解,即可以针对肿瘤恶性肿瘤进行的过程可能是重要的。 方法:我们批判性分析与a)Eph受体有关的文献,特别强调EphA2及其在癌症中的作用,b)Sam结构域,c)涉及EphA2-Sam的异型Sam-Sam相互作用。 结果:虽然文献数据表明EphA2-Sam与Ship2-Sam的结合应当在癌细胞中大量产生致癌作用,但是EphA2-Sam / Odin-Sam1复合物与该疾病之间的相关性尚不清楚。最近,包括来自Ship2-Sam和Odin-Sam1的结合界面的一些线性肽已经被表征,但是由于缺乏天然样折叠,未能有效地阻断涉及EphA2-Sam的异型Sam-Sam相互作用。 结论:异型EphA2-Sam协会的分子拮抗剂可以作为潜在的抗癌剂或作为工具进一步澄清受体功能,并最终验证其作为一个新的目标在抗癌药物发现领域的作用。由于线性肽的失败,迫切需要基于环状或螺旋分子的靶向Sam-Sam界面的新方法
关键词: 受体酪氨酸激酶,EphA2,Sam结构域,蛋白质 - 蛋白质相互作用,癌症,新型靶标。
Current Medicinal Chemistry
Title:The Sam Domain of EphA2 Receptor and its Relevance to Cancer: A Novel Challenge for Drug Discovery?
Volume: 23 Issue: 42
Author(s): Flavia A. Mercurio, Marilisa Leone
Affiliation:
关键词: 受体酪氨酸激酶,EphA2,Sam结构域,蛋白质 - 蛋白质相互作用,癌症,新型靶标。
摘要: Background: Eph receptors play important functions in developmental processes and diseases and among them EphA2 is well known for its controversial role in cancer. Drug discovery strategies are mainly centered on EphA2 extracellular ligand-binding domain however, the receptor also contains a largely unexplored cytosolic Sam (Sterile alpha motif) domain at the C-terminus. EphA2-Sam binds the Sam domain from the lipid phosphatase Ship2 and the first Sam domain of Odin. Sam-Sam interactions may be important to regulate ligand-induced receptor endocytosis and degradation i.e., processes that could be engaged against tumor malignancy.
Methods: We critically analyzed literature related to a) Eph receptors with particular emphasis on EphA2 and its role in cancer, b) Sam domains, c) heterotypic Sam-Sam interactions involving EphA2-Sam.
Results: While literature data indicate that binding of EphA2-Sam to Ship2-Sam should largely generate pro-oncogenic effects in cancer cells, the correlation between EphA2- Sam/Odin-Sam1 complex and the disease is unclear. Recently a few linear peptides encompassing binding interfaces from either Ship2-Sam and Odin-Sam1 have been characterized but failed to efficiently block heterotypic Sam-Sam interactions involving EphA2-Sam due to the lack of a native like fold.
Conclusion: Molecule antagonists of heterotypic EphA2-Sam associations could work as potential anticancer agents or be implemented as tools to further clarify receptor functions and eventually validate its role as a novel target in the field of anti-cancer drug discovery. Due to the failure of linear peptides there is a crucial need for novel approaches, based on cyclic or helical molecules, to target Sam-Sam interfaces.
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Cite this article as:
Flavia A. Mercurio, Marilisa Leone , The Sam Domain of EphA2 Receptor and its Relevance to Cancer: A Novel Challenge for Drug Discovery?, Current Medicinal Chemistry 2016; 23 (42) . https://dx.doi.org/10.2174/0929867323666161101100722
DOI https://dx.doi.org/10.2174/0929867323666161101100722 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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