Teel R W
Cancer Lett. 1986 Mar;30(3):329-36. doi: 10.1016/0304-3835(86)90058-3.
Ellagic acid (EA), a plant phenol, is reported to possess antimutagenic and anticarcinogenic activity. In the present study, explants of esophagus, trachea, colon, forestomach and bladder from young male Sprague-Dawley rats were incubated in medium containing [3H]EA (4.5 mu Ci/ml) for 24 h at 37 degrees C. DNA from these explants was extracted, purified and quantitated to determine [3H]EA binding to the DNA. Significant covalent binding of [3H]EA to DNA occurred in all the explants. Calf thymus DNA incubated in 0.05 M sodium phosphate buffer containing [3H]EA covalently bound [3H]EA in a concentration dependent manner. Furthermore covalent binding of [3H]EA to calf thymus DNA was inhibited by the addition of unlabeled EA that was concentration dependent over a range of 50-150 microM and by the addition of unlabeled adenosine, cytidine, guanosine or thymidine at a concentration of 1.0 mM. These results suggest that one of the mechanisms by which EA inhibits mutagenesis and carcinogenesis is by forming adducts with DNA, thus masking binding sites to be occupied by the mutagen or carcinogen.
鞣花酸(EA)是一种植物酚,据报道具有抗诱变和抗癌活性。在本研究中,将年轻雄性斯普拉格-道利大鼠的食管、气管、结肠、前胃和膀胱外植体在含有[3H]EA(4.5微居里/毫升)的培养基中于37℃孵育24小时。提取、纯化并定量这些外植体的DNA,以确定[3H]EA与DNA的结合情况。在所有外植体中均发生了[3H]EA与DNA的显著共价结合。在含有[3H]EA的0.05M磷酸钠缓冲液中孵育的小牛胸腺DNA以浓度依赖的方式共价结合[3H]EA。此外,添加未标记的EA(在50 - 150 microM范围内浓度依赖)以及添加浓度为1.0 mM的未标记腺苷、胞苷、鸟苷或胸苷可抑制[3H]EA与小牛胸腺DNA的共价结合。这些结果表明,EA抑制诱变和致癌作用的机制之一是与DNA形成加合物,从而掩盖诱变剂或致癌物将要占据的结合位点。