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

Author:

Sharma Nilesh Kumar1ORCID,Bahot Anjali1ORCID,Sekar Gopinath1ORCID,Bansode Mahima1,Khunteta Kratika1,Sonar Priyanka Vijay1ORCID,Hebale Ameya1,Salokhe Vaishnavi1ORCID,Sinha Birandra Kumar2

Affiliation:

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

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

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.

Funder

National Institute of Environmental Health Sciences, NIH

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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