二氢查耳酮类化合物对癌细胞的放射增敏作用。
Radiosensitization of cancer cells by hydroxychalcones.
机构信息
Department of Radiation Oncology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
出版信息
Bioorg Med Chem Lett. 2010 Oct 15;20(20):5997-6000. doi: 10.1016/j.bmcl.2010.08.081. Epub 2010 Aug 22.
Radiation sensitization is significantly increased by proteotoxic stress, such as a heat shock. We undertook an investigation, seeking to identify natural products that induced proteotoxic stress and then determined if a compound exhibited radiosensitizing properties. The hydroxychalcones, 2',5'-dihydroxychalcone (D-601) and 2,2'-dihydroxychalcone (D-501), were found to activate heat shock factor 1 (Hsf1) and exhibited radiation sensitization properties in colon and pancreatic cancer cells. The radiosensitization ability of D-601 was blocked by pretreatment with α-napthoflavone (ANF), a specific inhibitor of cytochrome P450 1A2 (CYP1A2), suggesting that the metabolite of D-601 is essential for radiosensitization. The study demonstrated the ability of hydroxychalcones to radiosensitize cancer cells and provides new leads for developing novel radiation sensitizers.
辐射增敏作用显著增加蛋白毒性应激,如热休克。我们进行了一项调查,旨在寻找诱导蛋白毒性应激的天然产物,然后确定一种化合物是否具有放射增敏特性。二氢查耳酮,2',5'-二羟基查耳酮(D-601)和 2,2'-二羟基查耳酮(D-501),被发现能激活热休克因子 1(Hsf1),并在结肠和胰腺癌细胞中表现出放射增敏特性。D-601 的放射增敏能力被α-萘黄酮(ANF)预处理所阻断,α-萘黄酮是细胞色素 P450 1A2(CYP1A2)的特异性抑制剂,这表明 D-601 的代谢物对放射增敏是必需的。该研究证明了二氢查耳酮类化合物对癌细胞的放射增敏作用,并为开发新型放射增敏剂提供了新的线索。