A review on endoplasmic reticulum-dependent anti-breast cancer activity of herbal drugs: possible challenges and opportunities.

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Journal of Drug Targeting Pub Date : 2025-02-01 Epub Date: 2024-10-24 DOI:10.1080/1061186X.2024.2417189
Mayank Kumar Choudhary, Bhaskaranand Pancholi, Manoj Kumar, Raja Babu, Debapriya Garabadu
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引用次数: 0

Abstract

Breast cancer (BC) is a major cause of cancer-related mortality across the globe and is especially highly prevalent in females. Based on the poor outcomes and several limitations of present management approaches in BC, there is an urgent need to focus and explore an alternate target and possible drug candidates against the target in the management of BC. The accumulation of misfolded proteins and subsequent activation of unfolded protein response (UPR) alters the homeostasis of endoplasmic reticulum (ER) lumen that ultimately causes oxidative stress in ER. The UPR activates stress-detecting proteins such as IRE1α, PERK, and ATF6, these proteins sometimes may lead to the activation of pro-apoptotic signaling pathways in cancerous cells. The ER stress-dependent antitumor activity could be achieved either through suppressing the adaptive UPR to make cells susceptible to ER stress or by causing chronic ER stress that may lead to triggering of pro-apoptotic signaling pathways. Several herbal drugs trigger ER-dependent apoptosis in BC cells. Therefore, this review discussed the role of fifty-two herbal drugs and their active constituents, focusing on disrupting the balance of the ER within cancer cells. Further, several challenges and opportunities have also been discussed in ER-dependent management in BC.Breast cancer (BC) is a major cause of cancer-related mortality across the globe and is especially highly prevalent in females. Based on the poor outcomes and several limitations of present management approaches in BC, there is an urgent need to focus and explore an alternate target and possible drug candidates against the target in the management of BC. The accumulation of misfolded proteins and subsequent activation of unfolded protein response (UPR) alters the homeostasis of endoplasmic reticulum (ER) lumen that ultimately causes oxidative stress in ER. The UPR activates stress-detecting proteins such as IRE1α, PERK, and ATF6, these proteins sometimes may lead to the activation of pro-apoptotic signaling pathways in cancerous cells. The ER stress-dependent antitumor activity could be achieved either through suppressing the adaptive UPR to make cells susceptible to ER stress or by causing chronic ER stress that may lead to triggering of pro-apoptotic signaling pathways. Several herbal drugs trigger ER-dependent apoptosis in BC cells. Therefore, this review discussed the role of fifty-two herbal drugs and their active constituents, focusing on disrupting the balance of the ER within cancer cells. Further, several challenges and opportunities have also been discussed in ER-dependent management in BC.

草药的内质网依赖性抗乳腺癌活性综述:可能的挑战和机遇。
乳腺癌(BC)是全球癌症相关死亡的主要原因,尤其是在女性中高发。乳腺癌的治疗包括化疗、放疗和手术。使用化疗药物治疗乳腺癌的成本很高,而且会产生一些不良反应。鉴于目前对 BC 的治疗效果不佳且存在一些局限性,因此迫切需要关注和探索治疗 BC 的替代靶点和针对该靶点的候选药物。内质网(ER)应激的产生会因错误折叠蛋白的积累而扰乱ER腔内的平衡,导致未折叠蛋白反应(UPR)的激活,其目的是恢复ER的平衡。然而,在ER应激灼烧的情况下,UPR会激活三种应激检测蛋白:IRE1α、PERK和ATF6,这些蛋白有时会导致癌细胞中促凋亡信号通路的激活。因此,通过调节ER应激达到抗肿瘤效果有两种途径:一是抑制适应性UPR,使细胞易受ER应激影响;二是引起慢性ER应激,从而触发促凋亡信号通路。以往的研究探索了几种草药及其活性成分,以提供有效、无毒、经济的抗癌疗法。越来越多的证据表明,有几种草药能触发 BC 细胞中的 ER 依赖性凋亡。因此,本综述讨论了 24 种中草药及其活性成分的作用,重点是破坏癌细胞内的 ER 平衡,从而通过调节 ER 应激相关蛋白反应诱导细胞凋亡。此外,还讨论了依赖ER的管理在BC中面临的一些挑战和机遇。
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
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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