Department of Vascular and Breast Surgery, First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, P.R. China.
School of Medical & Life Sciences, Chengdu University of TCM, Chengdu, Sichuan, P.R. China.
Cell Biochem Funct. 2020 Apr;38(3):249-256. doi: 10.1002/cbf.3443. Epub 2020 Feb 27.
Hinokiflavone is a natural product, isolated from Selaginella P. Beauv, Juniperus phoenicea and Rhus succedanea. Even though hinokiflavone was reported to possess cytotoxicity to many cancer cells, and has potential in cancer treatment, the anti-proliferation and anti-metastasis efficacy of hinokiflavone on human breast cancer cells has not a further research. In this study, we investigated the anti-cancer activity of hinokiflavone in human breast cancer cells in vitro and in vivo. Hinokiflavone exhibited a time- and dose-dependent manner apoptosis induction by upregulating expression of Bax and downregulating Bcl-2 in breast cancer cells. Furthermore, hinokiflavone significantly inhibited the migration and invasion of breast cancer cells by impairing the process of epithelial-to-mesenchymal transition. In addition, the tumour growth was distinctly inhibited by treatment of hinokiflavone in a xenograft tumour mouse model of MDA-MB-231 cells. Immunohistochemical analysis of tumour sections showed that MMP-2 cells and Ki-67 cells were remarkably decreased in tumour tissues of mice after treatment of hinokiflavone, indicating that hinokiflavone inhibits not only proliferation but also metastasis of breast cancer cells. Our study suggested that hinokiflavone can be a potential drug to breast cancer. SIGNIFICANCE OF THE STUDY: Hinokiflavone significantly inhibited proliferation and induced apoptosis in breast cancer cells. In addition, hinokiflavone remarkably inhibited migration and invasion of breast cancer cells via EMT signalling pathway. It is worth noting that hinokiflavone possesses anti-tumour effect in tumour mouse xenograft model of breast cancer. Overall, our results indicated that hinokiflavone may be a potential anticancer drug for breast cancer treatment.
扁柏黄酮是一种天然产物,从卷柏、柏木和漆树中分离得到。尽管扁柏黄酮已被报道对许多癌细胞具有细胞毒性,并具有癌症治疗的潜力,但扁柏黄酮对人乳腺癌细胞的抗增殖和抗转移作用尚未得到进一步研究。在这项研究中,我们研究了扁柏黄酮在体外和体内对人乳腺癌细胞的抗癌活性。扁柏黄酮通过上调 Bax 的表达和下调 Bcl-2 的表达,以时间和剂量依赖的方式诱导乳腺癌细胞凋亡。此外,扁柏黄酮通过抑制上皮间质转化过程显著抑制乳腺癌细胞的迁移和侵袭。此外,在 MDA-MB-231 细胞的异种移植肿瘤小鼠模型中,扁柏黄酮的治疗明显抑制了肿瘤的生长。肿瘤组织的免疫组织化学分析显示,扁柏黄酮治疗后肿瘤组织中的 MMP-2 细胞和 Ki-67 细胞明显减少,表明扁柏黄酮不仅抑制乳腺癌细胞的增殖,而且抑制其转移。我们的研究表明,扁柏黄酮可以成为一种治疗乳腺癌的潜在药物。研究意义:扁柏黄酮显著抑制乳腺癌细胞的增殖并诱导其凋亡。此外,扁柏黄酮通过 EMT 信号通路显著抑制乳腺癌细胞的迁移和侵袭。值得注意的是,扁柏黄酮在乳腺癌肿瘤小鼠异种移植模型中具有抗肿瘤作用。综上所述,我们的研究结果表明,扁柏黄酮可能是一种治疗乳腺癌的潜在抗癌药物。