School of Pharmacy, College of Medicine, National Taiwan University, Taipei, Taiwan.
J Nutr Biochem. 2011 Aug;22(8):732-40. doi: 10.1016/j.jnutbio.2010.06.004. Epub 2010 Nov 9.
Denbinobin (5-hydroxy-3,7-dimethoxy- 1,4-phenanthraquinone), a biologically active chemical isolated from Ephemerantha lonchophylla, has been demonstrated to display anti-cancer activity. Breast cancer is the leading cause of female mortality, and the high mortality is mainly attributable to metastasis. Src kinase activity is elevated in many human cancers, including breast cancer, and is often associated with aggressive disease. In the present study, we examined the anti-metastatic effects of denbinobin through decreasing Src kinase activity in human and mouse breast cancer cells. Denbinobin caused significant block of Src kinase activity in both human and mouse breast cancer cells. Moreover, phosphorylation of the signaling molecules focal adhesion kinase, Crk-associated substrate and paxillin downstream of Src was also inhibited by denbinobin. Furthermore, denbinobin inhibited the in vitro migration, invasion and in vivo metastasis of breast cancers in a mouse metastatic model. The denbinobin-treated group showed a significant reduction in tumor metastasis, orthrotopic tumor volume, and spleen enlargement compared to the control group. In addition, transfection of breast cancer cells with a plasmid coding for a constitutively active Src prevented the denbinobin-mediated phosphorylation of Src and downstream molecules and cell migration. Our findings provide evidences that denbinobin inhibits Src-mediated signaling pathways involved in controlling breast cancer migration and metastasis, suggesting that it has therapeutic potential in breast cancer treatment.
地诺孕素(5-羟基-3,7-二甲氧基-1,4-菲醌)是一种从Ephemerantha lonchophylla 中分离出来的具有生物活性的化学物质,已被证明具有抗癌活性。乳腺癌是女性死亡的主要原因,高死亡率主要归因于转移。Src 激酶活性在许多人类癌症中升高,包括乳腺癌,并且通常与侵袭性疾病相关。在本研究中,我们通过降低人类和小鼠乳腺癌细胞中的 Src 激酶活性来研究地诺孕素的抗转移作用。地诺孕素导致人类和小鼠乳腺癌细胞中的 Src 激酶活性显著受阻。此外,地诺孕素还抑制了 Src 下游的信号分子粘着斑激酶、Crk 相关底物和桩蛋白的磷酸化。此外,地诺孕素在小鼠转移模型中抑制了乳腺癌的体外迁移、侵袭和体内转移。与对照组相比,地诺孕素处理组的肿瘤转移、原位肿瘤体积和脾脏肿大均显著减少。此外,用编码组成性激活 Src 的质粒转染乳腺癌细胞可防止地诺孕素介导的 Src 和下游分子及细胞迁移的磷酸化。我们的研究结果提供了证据表明,地诺孕素抑制 Src 介导的信号通路,参与控制乳腺癌的迁移和转移,这表明它在乳腺癌治疗中具有治疗潜力。