Department of Oncology, Changsha Central Hospital, Shaoshan South Road 161, Changsha 410004, Hunan, PR China.
Department of Breast Surgery, Xiangya Hospital, Central South University, Xiangya Road 87, Changsha 410008, Hunan, PR China.
Biomed Pharmacother. 2016 Oct;83:526-535. doi: 10.1016/j.biopha.2016.06.049. Epub 2016 Jul 20.
Breast cancer (BC) is the foremost cause of cancer-related mortality in women worldwide. Polyporus umbellatus is a polysaccharide preparation of the Chinese traditional herb medicine, which has been explored as an inhibitory compounds in suppressing many cancers. And AKT has been known as an essential signaling pathway to regulate cell proliferation and apoptosis via Mdm2/p53 and Caspase-3 signaling pathways respectively. In our study, western blot, RT-PCR, immunochemical assay, immunofluorescence as well as flow cytometry were performed in vitro or in vivo to determine the effects of Polyporus umbellatus on the progression of human laryngeal cancer. First, the breast cancer cell growth, invasion and migration were inhibited, as well as the tumor volume in nude mice was down-regulated for Polyporus umbellatus use. Additionally, our data also showed that Polyporus umbellatus suppressed breast cancer cells proliferation, which was linked with the down-regulation of AKT activation by Polyporus umbellatus treatment. Mdm was inactivated while p53 was stimulated for Polyporus umbellatus administration, displaying inhibitory role in tumor growth. Furthermore, Polyporus umbellatus could up-regulate breast cancer cells in G0/G1 phase during cell cycle, and at the same time reducing cells in S phase. Also, flow cytometry and western blot assays suggested that apoptosis was induced by the administration of Polyporus umbellatus, which enhanced Caspase-3 expressions by AKT-regulated anti-apoptotic and pro-apoptotic signals. In conclusion, our data indicated that Polyporus umbellatus had a potential role in controlling human breast cancer through inhibiting tumor cell proliferation, inducing apoptosis regulated by AKT, which might provide a therapeutic strategy for breast cancer suppression in the future.
乳腺癌(BC)是全球女性癌症相关死亡的首要原因。云芝是一种中药多糖制剂,已被探索作为抑制多种癌症的化合物。AKT 已被认为是通过 Mdm2/p53 和 Caspase-3 信号通路分别调节细胞增殖和细胞凋亡的重要信号通路。在我们的研究中,通过体外和体内实验进行了 Western blot、RT-PCR、免疫化学测定、免疫荧光和流式细胞术,以确定云芝对人喉癌进展的影响。首先,云芝抑制了乳腺癌细胞的生长、侵袭和迁移,并降低了裸鼠的肿瘤体积。此外,我们的数据还表明,云芝通过抑制 AKT 激活来抑制乳腺癌细胞的增殖。云芝处理使 Mdm 失活而 p53 被激活,从而在肿瘤生长中发挥抑制作用。此外,云芝可以在细胞周期中将乳腺癌细胞上调至 G0/G1 期,同时减少 S 期的细胞。同样,流式细胞术和 Western blot 分析表明,云芝通过 AKT 调节的抗凋亡和促凋亡信号诱导细胞凋亡。总之,我们的数据表明,云芝通过抑制肿瘤细胞增殖、诱导 AKT 调节的凋亡,在控制人乳腺癌方面具有潜在作用,这可能为未来的乳腺癌抑制提供一种治疗策略。