Synlett 2023; 34(18): 2129-2158
DOI: 10.1055/a-2132-1356
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Modern Boron Chemistry: 60 Years of the Matteson Reaction

Boronic Acids and Beyond: ROS-Responsive Prodrugs as Tools for a Safer and More Effective Cancer Chemotherapy

Sofia A. G. Monteiro
,
Pedro M. P. Gois
,
This work was generously supported by the Portuguese Fundação para a Ciência e Tecnologia, Ministério da Ciência e da Tecnologia, Portugal [grants, 2022.06817.CEECIND (J.A.), PTDC/QUI-OUT/ 3989/2021 (P.G.); Institutional grants UIDB/04138/2020 and UIDP/04138/2020 (iMed)].


Abstract

Despite significant scientific advances and the wide variety of available treatments, cancer remains a major cause of death worldwide. Chemotherapy, which is frequently one of the first-line treatments, frequently suffers from low selectivity to cancer cells, leading to the appearance of important side effects. Thus, it becomes imperative to develop a new generation of targeted alternatives that spare the healthy tissues by delivering the cytotoxic payloads safely and selectively to cancer cells. In this respect, prodrugs that are activated by tumor-specific stimuli have attracted significant attention. Despite being a hallmark of cancer and present in high concentrations in cancer cells, reactive oxygen species (ROS) have been rather underexplored as a stimulus for the preparation of targeted prodrugs, particularly when compared with an acidic pH or glutathione. Despite their lower expression, ROS have recently been gaining substantial consideration, with various ROS-responsive prodrugs already reported with meaningful performances both in vitro and in vivo. This review aims to provide critical insights into this strategy by discussing the various available functional groups (with an important focus on boronic acids and their esters), their mechanisms of action, examples of their applications, advantages, limitations, and future challenges.

1 Introduction

2 Boronic Acids and Boronate Esters

2.1 Histone Deacetylase Inhibitors

2.2 DNA Alkylating Agents

2.3 Selective Estrogen Receptor Modulators and Selective Estrogen Receptor Degraders

2.4 ROS Inducers

2.5 Prodrugs Based on Other Types of Anticancer Drugs

3 Other ROS-Responsive Moieties

3.1 Thiazolidinones

3.2 1,3-Oxathiolanes

3.3 Selenium Ethers

3.4 Sulfur-Containing ROS-Responsive Moieties

4 Summary and Future Perspectives



Publikationsverlauf

Eingereicht: 14. Juni 2023

Angenommen nach Revision: 18. Juli 2023

Accepted Manuscript online:
18. Juli 2023

Artikel online veröffentlicht:
05. September 2023

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