Vats Prerna, Saini Chainsee, Baweja Bhavika, Srivastava Sandeep K, Kumar Ashok, Kushwah Atar Singh, Nema Rajeev
Department of Biosciences, Manipal University Jaipur, Dehmi Kalan, Jaipur- Ajmer Expressway, Jaipur, Rajasthan, 303007, India.
Department of Biochemistry, All India Institute of Medical Sciences (AIIMS), Bhopal, Saket Nagar, Bhopal, Madhya Pradesh, 462020, India.
Mol Cancer. 2025 Jun 18;24(1):180. doi: 10.1186/s12943-025-02353-3.
Aurora kinases, AURKA, AURKB, and AURKC, are serine/threonine kinases that play a vital role in regulating cell division and mitosis, particularly in the separation of chromosomes. These kinases are often overexpressed in human tumor cell lines, indicating their potential involvement in tumorigenesis. Preliminary evidence supports the use of Aurora kinase inhibitors for certain types of tumors, several AURKs inhibitors are currently under phase I and II trials. As a result, there is a growing interest in identifying small-molecule Aurora kinase inhibitors to develop as anti-cancer agents. The regulation of the cell cycle, including mitosis, is increasingly recognized as a key target in the fight against various forms of cancer. Novel drugs are being designed to inhibit the function of regulatory proteins, such as Aurora kinases, with the goal of creating personalized treatments. This review summarizes the biology of Aurora kinases in the context of cancer, integrating both preclinical and clinical data. It discusses the challenges and opportunities associated with using Aurora kinases to enhance cancer treatment. Future directions for Aurora kinase-based therapies include developing more selective inhibitors that minimize off-target effects and improve therapeutic efficacy. Researchers are also exploring combination therapies that use Aurora kinase inhibitors alongside other targeted treatments to overcome resistance and improve patient outcomes. Additionally, advancements in biomarker discovery are expected to facilitate the identification of patients most likely to benefit from Aurora kinase-targeted therapies, paving the way for more personalized approaches to cancer treatment.
极光激酶(AURKA、AURKB和AURKC)是丝氨酸/苏氨酸激酶,在调节细胞分裂和有丝分裂,特别是染色体分离过程中发挥着至关重要的作用。这些激酶在人类肿瘤细胞系中常常过度表达,表明它们可能参与肿瘤发生。初步证据支持将极光激酶抑制剂用于某些类型的肿瘤,目前几种极光激酶抑制剂正处于I期和II期试验阶段。因此,人们越来越有兴趣寻找小分子极光激酶抑制剂作为抗癌药物来开发。细胞周期的调控,包括有丝分裂,越来越被认为是对抗各种癌症的关键靶点。正在设计新型药物来抑制调节蛋白的功能,如极光激酶,目的是实现个性化治疗。这篇综述在癌症背景下总结了极光激酶的生物学特性,整合了临床前和临床数据。它讨论了使用极光激酶增强癌症治疗所面临的挑战和机遇。基于极光激酶的治疗的未来方向包括开发更具选择性的抑制剂,以尽量减少脱靶效应并提高治疗效果。研究人员也在探索联合疗法,将极光激酶抑制剂与其他靶向治疗联合使用,以克服耐药性并改善患者预后。此外,生物标志物发现方面的进展有望促进识别最有可能从极光激酶靶向治疗中受益的患者,为更个性化的癌症治疗方法铺平道路。