Winczyk K, Pawlikowski M, Karasek M
Department of Experimental Endocrinology and Hormone Diagnostics, Institute of Endocrinology, Medical University of Lodz, Poland.
J Pineal Res. 2001 Sep;31(2):179-82. doi: 10.1034/j.1600-079x.2001.310213.x.
The effects of melatonin and the thiazolinidinedione derivative CGP 52608 on apoptosis of Colon 38 cancer cells were investigated. Male mice were implanted subcutaneously with a suspension of Colon 38 cells. Ten days after induction of tumors, the animals were treated with melatonin or CGP 52608. Both substances were given in subcutaneous injections in daily doses of 10 or 100 microg in the evening for 6 days. The control group received solvent. The apoptotic cells were visualized in paraffin sections by means of the transferase-mediated dUTPnick end-labeling method. Both treatments increased significantly and to the same degree the number of apoptotic cells in tumors. This finding confirms our earlier observation that melatonin exerts a pro-apoptotic effect on murine colonic cancer cells. Moreover, because CGP 52608 is a ligand of RZR/ROR receptors and the latter are considered by some investigators as nuclear binding sites for melatonin, our data suggest the involvement of these receptors in the pro-apoptotic effect of melatonin.
研究了褪黑素和噻唑啉二酮衍生物CGP 52608对结肠38癌细胞凋亡的影响。将雄性小鼠皮下植入结肠38细胞悬液。诱导肿瘤10天后,用褪黑素或CGP 52608对动物进行治疗。两种物质均在傍晚皮下注射,每日剂量为10或100微克,共6天。对照组接受溶剂。通过转移酶介导的dUTP缺口末端标记法在石蜡切片中观察凋亡细胞。两种处理均显著且同等程度地增加了肿瘤中凋亡细胞的数量。这一发现证实了我们早期的观察结果,即褪黑素对小鼠结肠癌细胞具有促凋亡作用。此外,由于CGP 52608是RZR/ROR受体的配体,且一些研究人员认为后者是褪黑素的核结合位点,我们的数据表明这些受体参与了褪黑素的促凋亡作用。