Chalcone HTMC causes in vitro selective cytotoxicity, cell-cycle G 1 phase arrest through p53-dependent pathway in human lung adenocarcinoma A549 cells, and in vivo tumor growth suppression

JIUNN-LIANG KO2026-10-162026-10-162010-11-15Pure ID: 15028341Pure UUID: de7ccfe0-7704-4faa-a7dd-5863a428e08f10.1016/j.bmcl.2010.09.056https://www.scopus.com/pages/publications/77958065694https://scholars.csmu.edu.tw/handle/123456789/33161The present Letter identified 2′-hydroxy-2,3,4′,6′- tetramethoxychalcone (HTMC) as a potent in vitro cytotoxic agent with selective activity against cell lines derived from human lung cancer. In A549 lung adenocarcinoma cells, HTMC caused G1 phase cell-cycle arrest. HTMC treatment also led to an inhibition of cell-cycle regulatory proteins phosphorylation of cdc2 (Tyr15 and Tyr161) and Rb (Ser795 and Ser807/811), which was accompanied by the accumulation of tumor suppresser genes p53 and p21. In addition, in vivo data demonstrated that HTMC act as a tumor growth suppressing agent.5enChalcone HTMC causes in vitro selective cytotoxicity, cell-cycle G 1 phase arrest through p53-dependent pathway in human lung adenocarcinoma A549 cells, and in vivo tumor growth suppressionjournal article