作者: Kai Tang , Yi Lin , Li‐Ming Li , None
DOI: 10.1002/AR.22677
关键词:
摘要: Adramycin (ADM) resistance is an essential aspect of bladder cancer treatment failure and phenethyl isothiocyanate (PEITC) has been found to exhibit antitumor properties; however, the effect potential mechanism PEITC on ADM reversal not fully clear. The aim this study was explore role in cells underlying molecular mechanisms. In report, we identified human carcinoma T24/ADM cells, including increased drug sensitivity ADM, cell apoptosis rates, intracellular accumulation Rhodamine-123 (Rh-123), expression DNA topoisomerase II (Topo-II), a decreased multidrug gene (MDR1), resistance-associated protein (MRP1), bcl-2 glutathione s transferase π (GST-π).We also that there NF-κB, Survivin, Twist, p-Akt, PTEN p-JNK after for T24/ cells. results indicated might be used as therapeutic strategy through blocking Akt activating MAPK pathway carcinoma.