Aurora kinases signaling in cancer: from molecular perception to targeted therapies

IF 33.9 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Prerna Vats, Chainsee Saini, Bhavika Baweja, Sandeep K. Srivastava, Ashok Kumar, Atar Singh Kushwah, Rajeev Nema
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引用次数: 0

Abstract

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.
极光激酶信号在癌症中的作用:从分子感知到靶向治疗
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,特别是染色体分离中起重要作用。这些激酶在人类肿瘤细胞系中经常过度表达,表明它们可能参与肿瘤发生。初步证据支持极光激酶抑制剂用于某些类型的肿瘤,几种AURKs抑制剂目前正在进行I期和II期试验。因此,人们对确定小分子极光激酶抑制剂以开发抗癌药物的兴趣越来越大。细胞周期的调控,包括有丝分裂,越来越被认为是对抗各种形式癌症的关键靶点。新的药物被设计用来抑制调控蛋白的功能,比如极光激酶,目的是创造个性化的治疗方法。本文综述了极光激酶在癌症中的生物学作用,结合临床前和临床数据。它讨论了与使用极光激酶加强癌症治疗相关的挑战和机遇。未来基于极光激酶的治疗方向包括开发更多的选择性抑制剂,以最大限度地减少脱靶效应和提高治疗效果。研究人员还在探索使用极光激酶抑制剂和其他靶向治疗来克服耐药性并改善患者预后的联合疗法。此外,生物标志物发现的进步有望促进识别最有可能从Aurora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。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Cancer
Molecular Cancer 医学-生化与分子生物学
CiteScore
54.90
自引率
2.70%
发文量
224
审稿时长
2 months
期刊介绍: Molecular Cancer is a platform that encourages the exchange of ideas and discoveries in the field of cancer research, particularly focusing on the molecular aspects. Our goal is to facilitate discussions and provide insights into various areas of cancer and related biomedical science. We welcome articles from basic, translational, and clinical research that contribute to the advancement of understanding, prevention, diagnosis, and treatment of cancer. The scope of topics covered in Molecular Cancer is diverse and inclusive. These include, but are not limited to, cell and tumor biology, angiogenesis, utilizing animal models, understanding metastasis, exploring cancer antigens and the immune response, investigating cellular signaling and molecular biology, examining epidemiology, genetic and molecular profiling of cancer, identifying molecular targets, studying cancer stem cells, exploring DNA damage and repair mechanisms, analyzing cell cycle regulation, investigating apoptosis, exploring molecular virology, and evaluating vaccine and antibody-based cancer therapies. Molecular Cancer serves as an important platform for sharing exciting discoveries in cancer-related research. It offers an unparalleled opportunity to communicate information to both specialists and the general public. The online presence of Molecular Cancer enables immediate publication of accepted articles and facilitates the presentation of large datasets and supplementary information. This ensures that new research is efficiently and rapidly disseminated to the scientific community.
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