Institute of Natural Medicine, University of Toyama.
Biochemistry Department, Faculty of Pharmacy, Minia University.
Biol Pharm Bull. 2022;45(10):1564-1571. doi: 10.1248/bpb.b22-00508.
Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) is a potential target for inflammatory-breast cancer treatment as it participates in its pathogenesis, such as tumor initiation, progression, survival, metastasis, and recurrence. In this study, we aimed to discover a novel anti-cancer treatment from natural products by targeting NF-κB activity. Using the 4T1-NFκB-luciferase reporter cell line, we tested three pregnane glycosides extracted from the herb Caralluma tuberculata and discovered that Russelioside A markedly suppressed NF-κB activity in breast cancer. Russelioside A inhibited NF-κB (p65) transcriptional activity and its phosphorylation. Following NF-κB inhibition, Russelioside A exerted anti-proliferative and anti-metastatic effects in breast cancer cells in vitro. Moreover, it inhibited the NF-κB constitutive expression of downstream pathways, such as VEGF-b, MMP-9, and IL-6 in 4T1 cells. In addition, it reduced the metastatic capacity in a 4T1 breast cancer model in vivo. Collectively, our conclusions reveal that Russelioside A is an attractive natural compound for treating triple-negative breast cancer growth and metastasis through regulating NF-κB activation.
核因子 κB 轻链增强子的活化 B 细胞(NF-κB)是炎症性乳腺癌治疗的潜在靶点,因为它参与了肿瘤的发生、进展、存活、转移和复发等过程。在这项研究中,我们旨在通过靶向 NF-κB 活性,从天然产物中发现一种新的抗癌治疗方法。我们使用来自草药 Caralluma tuberculata 的三种孕烷糖苷提取物,通过 4T1-NFκB-荧光素酶报告细胞系进行测试,发现 Russelioside A 可显著抑制乳腺癌中的 NF-κB 活性。Russelioside A 抑制 NF-κB(p65)转录活性及其磷酸化。抑制 NF-κB 后,Russelioside A 在体外对乳腺癌细胞表现出抗增殖和抗转移作用。此外,它还抑制了 4T1 细胞中 VEGF-b、MMP-9 和 IL-6 等下游通路的 NF-κB 组成型表达。此外,它还降低了体内 4T1 乳腺癌模型的转移能力。综上所述,我们的结论表明,Russelioside A 是一种有吸引力的天然化合物,可通过调节 NF-κB 激活来治疗三阴性乳腺癌的生长和转移。