Advances in chalcone-based anticancer therapy: mechanisms, preclinical advances, and future perspectives.

IF 6 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Expert Opinion on Drug Discovery Pub Date : 2024-12-01 Epub Date: 2024-12-05 DOI:10.1080/17460441.2024.2436908
Shefali Chowdhary, Preeti, Shekhar, Nikita Gupta, Rajesh Kumar, Vipan Kumar
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引用次数: 0

Abstract

Introduction: Cancer remains a leading cause of death worldwide with traditional treatments like chemotherapy, and radiotherapy becoming less effective due to multidrug resistance (MDR). This highlights the necessity for novel chemotherapeutics like chalcone-based compounds, which demonstrate broad anti-cancer properties and target multiple pathways. These compounds hold promise for improving cancer treatment outcomes compared to existing therapies.

Areas covered: This review provides a comprehensive synopsis of the recent literature (2018-2024) for anti-proliferative/anti-cancer activity of chalcones. It includes the identification of potential targets, their mechanisms of action, and possible modes of binding. Additionally, chalcone derivatives in preclinical trials are also discussed.

Expert opinion: Chalcones mark a significant stride in anticancer therapies due to their multifaceted approach in targeting various cellular pathways. Their ability to simultaneously target multiple pathways enables them to overcome drug resistance as compared to traditional therapies. With well-defined mechanisms of action, these compounds can serve as lead molecules for designing new, more promising treatments. Continued progress in synthesis and structural optimization, along with promising results from preclinical trials, offers hope for the development of more potent molecules, heralding a new era in cancer therapeutics.

基于查尔酮的抗癌治疗进展:机制、临床前进展和未来展望。
导言:癌症仍然是世界范围内导致死亡的主要原因,传统治疗方法如化疗和放疗由于多药耐药(MDR)而变得不那么有效。这突出了新型化疗药物的必要性,如查尔酮类化合物,它们具有广泛的抗癌特性,并针对多种途径。与现有疗法相比,这些化合物有望改善癌症治疗效果。研究领域:本文综述了查尔酮抗增殖/抗癌活性的最新文献(2018-2024)。它包括潜在靶标的识别,它们的作用机制和可能的结合模式。此外,查尔酮衍生物在临床前试验也进行了讨论。结论:查尔酮标志着抗癌治疗的一个重大进展,因为它们的多方面的方法针对不同的细胞途径。与传统疗法相比,它们同时靶向多种途径的能力使它们能够克服耐药性。由于具有明确的作用机制,这些化合物可以作为设计新的、更有前景的治疗方法的先导分子。合成和结构优化方面的持续进展,以及临床前试验的良好结果,为开发更多有效分子提供了希望,预示着癌症治疗的新时代。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.20
自引率
1.60%
发文量
78
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Drug Discovery (ISSN 1746-0441 [print], 1746-045X [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on novel technologies involved in the drug discovery process, leading to new leads and reduced attrition rates. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering chemoinformatics; bioinformatics; assay development; novel screening technologies; in vitro/in vivo models; structure-based drug design; systems biology Drug Case Histories examining the steps involved in the preclinical and clinical development of a particular drug The audience consists of scientists and managers in the healthcare and pharmaceutical industry, academic pharmaceutical scientists and other closely related professionals looking to enhance the success of their drug candidates through optimisation at the preclinical level.
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