| Literature DB >> 27097871 |
Jia-Wen Zhai1,2,3, Chang Gao4, Wei-Dong Ma1,2,3, Wei Wang1,2,3, Li-Ping Yao1,2,3, Xin-Xin Xia1,2,3, Meng Luo1,2,3, Yuan-Gang Zu1,2,3, Yu-Jie Fu1,2,3.
Abstract
Geraniin, a typical ellagitannin isolated from Phyllanthus urinaria Linn, has been found to possess a range of bioactive properties. In the present study, we found that Geraniin showed potent anti-proliferative effects on human breast cancer MCF-7 cells. The IC50 values were 9.94, 17.98 and 42.32 µM after 72-, 48- and 24-h treatment, respectively. Meanwhile, Geraniin could remarkably disrupt mitochondrial membrane potential and arrest S phase cell cycle. Western-blot analysis showed that Geraniin induced phosphorylation of the anti-apoptotic Bcl-2, and the cleavage of poly (ADP-ribose) polymerase (PARP) and caspase-3 in MCF-7 cells. Moreover, Geraniin treatment activated p38 mitogen-activated protein kinase (p38 MAPK) and the effect was blunted in MCF-7 cells with the treatment of a specific p38 inhibitor SB203580. Geraniin could generate intracellular reactive oxygen species (ROS), activate p38 MAPK then induce the apoptosis in MCF-7 cells, such phenomena was abrogated by pretreatment with N-acetyl-l-cysteine. In general, these results support the conclusion that Geraniin-induced apoptosis is mediated via ROS-mediated stimulation of p38 MAPK signaling.Entities:
Keywords: Apoptosis; MCF-7 cells; ROS; geraniin; mitochondrial; p38 MAPK
Mesh:
Substances:
Year: 2016 PMID: 27097871 DOI: 10.3109/15376516.2016.1139025
Source DB: PubMed Journal: Toxicol Mech Methods ISSN: 1537-6516 Impact factor: 2.987