| Literature DB >> 26368671 |
Si Tan1, Xin Guan2, Christoph Grün3, Zhiqin Zhou4, Ute Schepers5, Peter Nick6.
Abstract
Cancer cells divide rapidly, providing medical targets for anticancer agents. The polyphenolic gallic acid (GA) is known to be toxic for certain cancer cells. However, the cellular mode of action has not been elucidated. Therefore, the current study addressed a potential effect of GA on the mitosis of cancer cells. GA inhibited viability of HeLa cells in a dose-dependent and time-dependent manner. We could show, using fluorescence-activated cell sorting (FACS), that this inhibition was accompanied by elevated frequency of cells arrested at the G2/M transition. This cell-cycle arrest was accompanied by mitotic catastrophe, and formation of cells with multiple nuclei. These aberrations were preceded by impaired centrosomal clustering. We arrive at a model of action, where GA inhibits the progression of the cell cycle at the G2/M phase by impairing centrosomal clustering which will stimulate mitotic catastrophe. Thus, GA has potential as compound against cervical cancer.Entities:
Keywords: Cell-cycle arrest; Centrosome clustering; Gallic acid (GA); HeLa; Mitotic catastrophe
Mesh:
Substances:
Year: 2015 PMID: 26368671 DOI: 10.1016/j.tiv.2015.09.011
Source DB: PubMed Journal: Toxicol In Vitro ISSN: 0887-2333 Impact factor: 3.500