Hu Minghui, Zhang Yingyu, Zhang Pin, Liu Kangbo, Zhang Mengxin, Li Lifeng, Yu Zhidan, Zhang Xianwei, Zhang Wancun, Xu Ying
Health Commission of Henan Province Key Laboratory for Precision Diagnosis and Treatment of Pediatric Tumor, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou, 450018, China.
Henan Key Laboratory of Rare Diseases, Endocrinology and Metabolism Center, The First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang, 471003, China.
Protein Pept Lett. 2025;32(1):18-33. doi: 10.2174/0109298665338519241114103223.
With the emergence of the precision medicine era, targeting specific proteins has emerged as a pivotal breakthrough in tumor diagnosis and treatment. Apurinic/apyrimidinic Endonuclease 1 (APE1) is a multifunctional protein that plays a crucial role in DNA repair and cellular redox regulation. This article comprehensively explores the fundamental mechanisms of APE1 as a multifunctional enzyme in biology, with particular emphasis on its potential significance in disease diagnosis and strategies for tumor treatment. Firstly, this article meticulously analyzes the intricate biological functions of APE1 at a molecular level, establishing a solid theoretical foundation for subsequent research endeavors. In terms of diagnostic applications, the presence of APE1 can be detected in patient serum samples, biopsy tissues, and through cellular in situ testing. The precise detection methods enable changes in APE1 levels to serve as reliable biomarkers for predicting tumor occurrence, progression, and patient prognosis. Moreover, this article focuses on elucidating the potential role of APE1 in tumor treatment by exploring various inhibitors, including nucleic acid-based inhibitors and small molecule drug inhibitors categories, and revealing their unique advantages in disrupting DNA repair function and modulating oxidative-reduction activity. Finally, the article provides an outlook on future research directions for APE1 while acknowledging major technical difficulties and clinical challenges that need to be overcome despite its immense potential as a target for tumor therapy.
随着精准医学时代的到来,靶向特定蛋白质已成为肿瘤诊断和治疗的关键突破。脱嘌呤/脱嘧啶核酸内切酶1(APE1)是一种多功能蛋白质,在DNA修复和细胞氧化还原调节中起关键作用。本文全面探讨了APE1作为一种多功能酶在生物学中的基本机制,特别强调了其在疾病诊断中的潜在意义以及肿瘤治疗策略。首先,本文在分子水平上细致分析了APE1复杂的生物学功能,为后续研究奠定了坚实的理论基础。在诊断应用方面,可以在患者血清样本、活检组织中检测到APE1的存在,也可通过细胞原位检测来实现。这些精确的检测方法使APE1水平的变化能够作为预测肿瘤发生、进展和患者预后的可靠生物标志物。此外,本文着重通过探索各种抑制剂来阐明APE1在肿瘤治疗中的潜在作用,这些抑制剂包括基于核酸的抑制剂和小分子药物抑制剂等类别,并揭示它们在破坏DNA修复功能和调节氧化还原活性方面的独特优势。最后,本文在认识到APE1作为肿瘤治疗靶点虽具有巨大潜力但仍需克服主要技术难题和临床挑战的同时,对其未来的研究方向进行了展望。