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BRCT Domains: Structure, Functions, and Implications in Disease-New Therapeutic Targets for Innovative Drug Discovery against Infections

期刊

PHARMACEUTICS
卷 15, 期 7, 页码 -

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MDPI
DOI: 10.3390/pharmaceutics15071839

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BRCT; infection; disease; cancer; leishmania; therapeutic target; drug

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The BRCT domain is a potential therapeutic target due to its moderately conserved folding and high sequence variations. It plays critical roles in DNA repair, recombination, and cell cycle control, and is implicated in various pathologic processes including breast, ovarian, and lung cancer. This review explores the possible roles of BRCT domains as therapeutic targets and describes their common structural features, relevant interactions and pathways, as well as their implications in pathologic processes. Additionally, it presents drugs commonly used to target these domains and offers new drug design possibilities based on their structures.
The search for new therapeutic targets and their implications in drug development remains an emerging scientific topic. BRCT-bearing proteins are found in Archaea, Bacteria, Eukarya, and viruses. They are traditionally involved in DNA repair, recombination, and cell cycle control. To carry out these functions, BRCT domains are able to interact with DNA and proteins. Moreover, such domains are also implicated in several pathogenic processes and malignancies including breast, ovarian, and lung cancer. Although these domains exhibit moderately conserved folding, their sequences show very low conservation. Interestingly, sequence variations among species are considered positive traits in the search for suitable therapeutic targets, since non-specific drug interactions might be reduced. These main characteristics of BRCT, as well as its critical implications in key biological processes in the cell, have prompted the study of these domains as therapeutic targets. This review explores the possible roles of BRCT domains as therapeutic targets for drug discovery. We describe their common structural features and relevant interactions and pathways, as well as their implications in pathologic processes. Drugs commonly used to target these domains are also presented. Finally, based on their structures, we describe new drug design possibilities using modern and innovative techniques.

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