Biflavonoids: Preliminary Reports on Their Role in Prostate and Breast Cancer Therapy

Pharmaceuticals Pub Date : 2024-07-02 DOI:10.3390/ph17070874
Carolina Afonso de Lima, Larissa Kaori Maquedano, Luiza Sertek Jaalouk, Dina Cardoso dos Santos, G. Longato
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Abstract

Dimeric flavonoids, also called biflavonoids, are bioactive compounds that exhibit various activities described in the literature, including antibacterial, antifungal, antiviral, anti-inflammatory, analgesic, antioxidant, vasorelaxant, and anticancer properties. This work focuses on the anticancer action of naturally occurring dimeric flavonoids against prostate and breast cancer, as well as on the mechanisms of action involved in their activity and presents the most current information on this subject in the literature. In the present review, we summarize the latest findings on the antiproliferative activity of 33 dimeric flavonoid-based compounds selected from recently published studies. The tests conducted were in silico and in vitro and demonstrated the cytotoxic activity potential of biflavonoids against prostate and breast tumor cells. Biflavonoids were capable of interfering with the migration and replication of cancer cells and their mechanism of action is related to cell death pathways, especially apoptosis, necrosis, and ferroptosis. These compounds decreased mitochondrial membrane potential and significantly increased intracellular levels of reactive oxygen species (ROS). Additionally, they significantly upregulated the expression of p21, Bax, and cleaved caspase-3, while downregulating Bcl-2 and caspase-3 levels, indicating their cell death mechanism of action is through the Bcl-2/Bax/cleaved caspase-3 pathway and cell cycle arrest. The biflavonoids here related have shown promising anticancer activity and are considered potential drug candidates for prostate and breast cancer treatment.
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双黄酮:关于其在前列腺癌和乳腺癌治疗中作用的初步报告
二聚类黄酮又称双黄酮,是一种生物活性化合物,具有文献中描述的各种活性,包括抗菌、抗真菌、抗病毒、抗炎、镇痛、抗氧化、血管舒张和抗癌特性。本研究主要关注天然二聚黄酮类化合物对前列腺癌和乳腺癌的抗癌作用,以及这些化合物的作用机制,并介绍了目前文献中有关这一主题的最新信息。在本综述中,我们总结了从最近发表的研究中选出的 33 种基于二聚类黄酮的化合物的抗增殖活性的最新发现。所进行的测试包括硅学测试和体外测试,结果表明双黄酮类化合物对前列腺和乳腺肿瘤细胞具有潜在的细胞毒性活性。双黄酮类化合物能够干扰癌细胞的迁移和复制,其作用机制与细胞死亡途径有关,特别是细胞凋亡、坏死和铁凋亡。这些化合物会降低线粒体膜电位,并显著增加细胞内活性氧(ROS)的水平。此外,它们还能明显上调 p21、Bax 和裂解的 caspase-3 的表达,同时下调 Bcl-2 和 caspase-3 的水平,这表明它们的细胞死亡作用机制是通过 Bcl-2/Bax/ 裂解的 caspase-3 途径和细胞周期停滞。与此相关的双黄酮类化合物具有良好的抗癌活性,被认为是治疗前列腺癌和乳腺癌的潜在候选药物。
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