a Department of Colorectal and Anal Surgery , The First Hospital of Jilin University , Changchun , Jilin , 130021 , China.
Cell Cycle. 2018;17(2):240-249. doi: 10.1080/15384101.2017.1407892. Epub 2018 Jan 5.
Paeoniflorin (PF) exhibits tumor suppressive functions in a variety of human cancers. However, the function of PF and molecular mechanism in colorectal cancer are elusive. In the present study, we investigated whether PF could exert its antiproliferative activity, anti-migration, and anti-invasive function in colorectal cancer cells. We found that PF inhibited cell growth and induced apoptosis and blocked cell cycle progression in the G0/G1 phase in colorectal cancer cells. Moreover, we found that PF suppressed cell migration and invasion in colorectal cancer cells. FoxM1 has been reported to play an important oncogenic role in human cancers. We also determine whether PF inhibited the expression of FoxM1, leading to its anti-cancer activity. We found that PF treatment in colorectal cancer cells resulted in down-regulation of FoxM1. The rescue experiments showed that overexpression of FoxM1 abrogated the tumor suppressive function induced by PF treatment. Notably, depletion of FoxM1 promoted the anti-tumor activity of PF in colorectal cancer cells. Therefore, inhibition of FoxM1 could participate in the anti-tumor activity of PF in colorectal cancer cells.
芍药苷(PF)在多种人类癌症中具有肿瘤抑制功能。然而,PF 在结直肠癌中的功能和分子机制尚不清楚。在本研究中,我们研究了 PF 是否可以在结直肠癌细胞中发挥其抗增殖活性、抗迁移和抗侵袭功能。我们发现 PF 抑制细胞生长并诱导细胞凋亡,同时将细胞周期阻滞在 G0/G1 期。此外,我们发现 PF 抑制结直肠癌细胞的迁移和侵袭。FoxM1 已被报道在人类癌症中发挥重要的致癌作用。我们还确定 PF 是否抑制 FoxM1 的表达,从而发挥其抗癌活性。我们发现 PF 处理结直肠癌细胞导致 FoxM1 的下调。挽救实验表明,FoxM1 的过表达可消除 PF 处理诱导的肿瘤抑制功能。值得注意的是,FoxM1 的耗竭促进了 PF 在结直肠癌细胞中的抗肿瘤活性。因此,抑制 FoxM1 可能参与 PF 在结直肠癌细胞中的抗肿瘤活性。