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了解癌症对拓扑异构酶活性药物的防御机制:全面综述。

Understanding Cancer's Defense against Topoisomerase-Active Drugs: A Comprehensive Review.

作者信息

Sharma Nilesh Kumar, Bahot Anjali, Sekar Gopinath, Bansode Mahima, Khunteta Kratika, Sonar Priyanka Vijay, Hebale Ameya, Salokhe Vaishnavi, Sinha Birandra Kumar

机构信息

Cancer and Translational Research Centre Dr. D.Y. Patil Biotechnology & Bioinformatics Institute, Dr. D.Y. Patil Vidyapeeth, Pune 411033, Maharashtra, India.

Mechanistic Toxicology Branch, Division of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, Durham, NC 27709, USA.

出版信息

Cancers (Basel). 2024 Feb 6;16(4):680. doi: 10.3390/cancers16040680.

Abstract

In recent years, the emergence of cancer drug resistance has been one of the crucial tumor hallmarks that are supported by the level of genetic heterogeneity and complexities at cellular levels. Oxidative stress, immune evasion, metabolic reprogramming, overexpression of ABC transporters, and stemness are among the several key contributing molecular and cellular response mechanisms. Topo-active drugs, e.g., doxorubicin and topotecan, are clinically active and are utilized extensively against a wide variety of human tumors and often result in the development of resistance and failure to therapy. Thus, there is an urgent need for an incremental and comprehensive understanding of mechanisms of cancer drug resistance specifically in the context of topo-active drugs. This review delves into the intricate mechanistic aspects of these intracellular and extracellular topo-active drug resistance mechanisms and explores the use of potential combinatorial approaches by utilizing various topo-active drugs and inhibitors of pathways involved in drug resistance. We believe that this review will help guide basic scientists, pre-clinicians, clinicians, and policymakers toward holistic and interdisciplinary strategies that transcend resistance, renewing optimism in the ongoing battle against cancer.

摘要

近年来,癌症耐药性的出现一直是关键的肿瘤特征之一,这在细胞水平上受到遗传异质性和复杂性的影响。氧化应激、免疫逃逸、代谢重编程、ABC转运蛋白的过表达以及干性是几个关键的分子和细胞反应机制。拓扑异构酶活性药物,如阿霉素和拓扑替康,在临床上具有活性,被广泛用于治疗多种人类肿瘤,但常常导致耐药性的产生和治疗失败。因此,迫切需要更深入、全面地了解癌症耐药机制,特别是在拓扑异构酶活性药物的背景下。本综述深入探讨了这些细胞内和细胞外拓扑异构酶活性药物耐药机制的复杂机理,并探索了通过使用各种拓扑异构酶活性药物和耐药相关途径抑制剂的潜在联合方法。我们相信,本综述将有助于指导基础科学家、临床前研究人员、临床医生和政策制定者制定超越耐药性的整体和跨学科策略,在对抗癌症的持续斗争中重拾乐观态度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/26b9/10886629/b8f9d3936619/cancers-16-00680-g001.jpg

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