Choudhary Mayank Kumar, Pancholi Bhaskaranand, Kumar Manoj, Babu Raja, Garabadu Debapriya
Department of Pharmacology, School of Health Sciences, Central University of Punjab, Bathinda, India.
J Drug Target. 2025 Feb;33(2):206-231. doi: 10.1080/1061186X.2024.2417189. Epub 2024 Oct 24.
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.
乳腺癌(BC)是全球癌症相关死亡的主要原因,在女性中尤为高发。鉴于目前乳腺癌管理方法的不良结果和若干局限性,迫切需要关注并探索替代靶点以及针对该靶点的潜在候选药物,以用于乳腺癌的管理。错误折叠蛋白的积累以及随后未折叠蛋白反应(UPR)的激活会改变内质网(ER)腔的稳态,最终导致内质网中的氧化应激。UPR会激活IRE1α、PERK和ATF6等应激检测蛋白,这些蛋白有时可能会导致癌细胞中促凋亡信号通路的激活。内质网应激依赖性抗肿瘤活性可以通过抑制适应性UPR使细胞对内质网应激敏感来实现,或者通过引起慢性内质网应激来实现,慢性内质网应激可能导致促凋亡信号通路的触发。几种草药药物会引发乳腺癌细胞中内质网依赖性凋亡。因此,本综述讨论了52种草药药物及其活性成分的作用,重点是破坏癌细胞内质网的平衡。此外,还讨论了乳腺癌内质网依赖性管理中的若干挑战和机遇。乳腺癌(BC)是全球癌症相关死亡的主要原因,在女性中尤为高发。鉴于目前乳腺癌管理方法的不良结果和若干局限性,迫切需要关注并探索替代靶点以及针对该靶点的潜在候选药物,以用于乳腺癌的管理。错误折叠蛋白的积累以及随后未折叠蛋白反应(UPR)的激活会改变内质网(ER)腔的稳态,最终导致内质网中的氧化应激。UPR会激活IRE1α、PERK和ATF6等应激检测蛋白,这些蛋白有时可能会导致癌细胞中促凋亡信号通路的激活。内质网应激依赖性抗肿瘤活性可以通过抑制适应性UPR使细胞对内质网应激敏感来实现,或者通过引起慢性内质网应激来实现,慢性内质网应激可能导致促凋亡信号通路的触发。几种草药药物会引发乳腺癌细胞中内质网依赖性凋亡。因此,本综述讨论了52种草药药物及其活性成分的作用,重点是破坏癌细胞内质网的平衡。此外,还讨论了乳腺癌内质网依赖性管理中的若干挑战和机遇。