| Literature DB >> 24858379 |
Jung Jae Cho1, Jung-Il Chae2, Goo Yoon1, Ka Hwi Kim1, Jin Hyoung Cho2, Seung-Sik Cho1, Young Sik Cho3, Jung-Hyun Shim1.
Abstract
Licochalcone A (LCA), a chalconoid derived from root of Glycyrrhiza inflata, has been known to possess a wide range of biological functions such as antitumor, anti-angiogenesis, antiparasitic, anti-oxidant, antibacterial and anti-inflammatory effects. However, the anticancer effects of LCA on oral squamous cell carcinoma (OSCC) have not been reported. Our data showed that LCA inhibited OSCC cell (HN22 and HSC4) growth in a concentration- and time-dependent manner. Mechanistically, it was mediated via downregulation of specificity protein 1 (Sp1) expression and subsequent regulation of Sp1 downstream proteins such as p27, p21, cyclin D1, Mcl-1 and survivin. Here, we found that LCA caused apoptotic cell death in HSC4 and HN22 cells, as characterized by sub-G1 population, nuclear condensation, Annexin V staining, and multi-caspase activity and apoptotic regulatory proteins such as Bax, Bid, Bcl(-xl), caspase-3 and PARP. Consequently, this study strongly suggests that LCA induces apoptotic cell death of OSCC cells via downregulation of Sp1 expression, prompting its potential use for the treatment of human OSCC.Entities:
Mesh:
Substances:
Year: 2014 PMID: 24858379 DOI: 10.3892/ijo.2014.2461
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650