Multidrug Resistance: Are We Still Afraid of the Big Bad Wolf.

IF 4.8 3区 医学 Q2 CHEMISTRY, MEDICINAL
Pharmaceuticals Pub Date : 2025-06-14 DOI:10.3390/ph18060895
Abdulelah Alhazza, Adenike Oyegbesan, Emira Bousoik, Hamidreza Montazeri Aliabadi
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引用次数: 0

Abstract

After the era of multidrug resistance (MDR) against cytotoxic chemotherapy, the development of resistance against newly developed molecularly targeted drugs also seems inevitable. While the mechanisms involved in resistance against these two categories of anticancer drugs are different, the principles are similar: inherent resistance (also known as primary resistance) is a result of heterogeneity in cancer cells where a subpopulation of the cells do not show a favorable initial response to the drug, while acquired resistance (or secondary resistance), as the name suggests, is developed after repeated treatments due to the plasticity of cancer cells. Despite the introduction of a variety of molecularly targeted drugs to clinical practice, chemotherapy is still at the forefront of the battle against cancer. In this manuscript, we review the major mechanisms involved in MDR and resistance against different categories of molecularly targeted drugs separately, and review some of the strategies studied to overcome the resistance against cancer therapy. While MDR mechanisms have been reviewed previously, the molecular mechanisms of resistance to the latest generations of anticancer drugs are rarely reviewed as a group, and the connection between the two categories of resistance is often missing in this type of publication. Our aim is to illustrate a comprehensive picture of what the landscape of cancer treatment is today with respect to resistance. While this picture seems bleak, and it is the common belief that resistance is inevitable, understanding the mechanisms involved could potentially lead to more efficient approaches to overcoming this so far unbeatable obstacle.

多药耐药性:我们还害怕大灰狼吗?
在对细胞毒性化疗的多药耐药(MDR)时代之后,对新开发的分子靶向药物的耐药发展似乎也不可避免。虽然对这两类抗癌药物的耐药机制不同,但原理是相似的:固有耐药(也称为原发性耐药)是癌细胞异质性的结果,其中一部分细胞对药物没有良好的初始反应,而获得性耐药(或继发性耐药),顾名思义,是由于癌细胞的可塑性而经过反复治疗后产生的。尽管在临床实践中引入了各种分子靶向药物,但化疗仍然处于对抗癌症的最前沿。在这篇文章中,我们分别综述了耐多药和对不同类别分子靶向药物的耐药的主要机制,并综述了一些研究克服癌症治疗耐药的策略。虽然以前已经对耐多药机制进行了综述,但对最新一代抗癌药物耐药的分子机制很少作为一个群体进行综述,而且在这类出版物中往往缺少两类耐药之间的联系。我们的目的是要说明什么景观癌症治疗是今天的耐药性的综合图片。尽管这一前景似乎令人沮丧,而且人们普遍认为阻力是不可避免的,但了解其中的机制可能会带来更有效的方法来克服这一迄今为止无法克服的障碍。
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
Pharmaceuticals
Pharmaceuticals Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
6.10
自引率
4.30%
发文量
1332
审稿时长
6 weeks
期刊介绍: Pharmaceuticals (ISSN 1424-8247) is an international scientific journal of medicinal chemistry and related drug sciences.Our aim is to publish updated reviews as well as research articles with comprehensive theoretical and experimental details. Short communications are also accepted; therefore, there is no restriction on the maximum length of the papers.
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