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The Ubiquitin-Proteasome Pathway an Emerging Anticancer Strategy for Therapeutics: A Patent Analysis

机译:泛素-蛋白酶体途径的新兴治疗癌症策略:专利分析

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The degradation of intracellular proteins is targeted by ubiquitin via non-lysosomal proteolytic pathway in the cell system. These ubiquitin molecules have been found to be conserved from yeast to humans. Ubiquitin proteasome machinery utilises ATP and other mechanisms for degrading proteins of cytosol as well as nucleus. This process of ubiquitination is regulated by activating the E3 enzyme ligase, involved in phosphorylation. In humans, proteins which regulate the cell cycle are controlled by ubiquitin; therefore the ubiquitin-proteasome pathway can be targeted for novel anti-cancer strategies. Dysregulation of the components of the ubiquitin system has been linked to many diseases like cancer and inflammation. The primary triggering mechanism (apoptosis) of these diseases can also be induced when TNF-related apoptosis-inducing ligand (TRAIL) binds to its specific receptor DR4 and DR5. In this review, the emerging prospects and importance of ubiquitin proteasome pathway as an evolving anticancer strategy have been discussed. Current challenges in the field of drug discovery have also been discussed on the basis of recent patents on cancer diagnosis and therapeutics.
机译:泛素通过细胞系统中的非溶酶体蛋白水解途径靶向细胞内蛋白质的降解。已经发现这些泛素分子从酵母到人类都是保守的。泛素蛋白酶体机制利用ATP和其他机制降解细胞质和细胞核蛋白。泛素化的过程通过激活参与磷酸化的E3酶连接酶来调节。在人类中,调节细胞周期的蛋白质受泛素控制。因此,泛素-蛋白酶体途径可以作为新型抗癌策略的靶标。泛素系统组分的失调与许多疾病如癌症和炎症有关。当TNF相关的凋亡诱导配体(TRAIL)与其特异性受体DR4和DR5结合时,也可以诱导这些疾病的主要触发机制(细胞凋亡)。在这篇综述中,已讨论了泛素蛋白酶体途径作为发展中的抗癌策略的新兴前景和重要性。在有关癌症诊断和治疗的最新专利的基础上,还讨论了药物发现领域的当前挑战。

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