Wawryk-Gawda Ewelina, Chylińska-Wrzos Patrycja, Lis-Sochocka Marta, Chłapek Katarzyna, Bulak Kamila, Jędrych Marian, Jodłowska-Jędrych Barbara
Department of Histology and Embryology with Experimental Cytology Unit, Medical University in Lublin, ul. Radziwiłłowska 11, 20-080, Lublin, Poland,
Protoplasma. 2014 May;251(3):525-33. doi: 10.1007/s00709-013-0548-1. Epub 2013 Sep 17.
The p53 protein is an important factor of many intra- and extracellular processes. This protein regulates the repair of cellular DNA and induces apoptosis. It is also responsible for the regulation of the senescence and the cell entering the subsequent stages of the cellular cycle. The protein p53 is also involved in inhibiting angiogenesis and the induction of oxidative shock. In our study, we examined the activity of p53 protein in the uterine epithelial cells in rats treated with cladribine. Its action is mainly based on apoptosis induction. We compared the activity of p53 protein in cells with a high apoptosis index and in cells with active repair mechanisms and high proliferation index. We observed stronger p53 protein expression in the epithelial cells of the materials taken 24 h after the last dose of 2-CdA associated with the active process of apoptosis and inhibition of proliferation. After 4 weeks from the last dose of cladribine, the stronger expression of p53 protein was associated with both the existing changes in the cell's genome, the effects of the ongoing repair mechanisms, as well as the high proliferation activity.
p53蛋白是许多细胞内和细胞外过程的重要因素。该蛋白调节细胞DNA的修复并诱导细胞凋亡。它还负责调节细胞衰老以及细胞进入细胞周期的后续阶段。p53蛋白还参与抑制血管生成和诱导氧化应激。在我们的研究中,我们检测了用克拉屈滨处理的大鼠子宫上皮细胞中p53蛋白的活性。其作用主要基于诱导细胞凋亡。我们比较了具有高凋亡指数的细胞以及具有活跃修复机制和高增殖指数的细胞中p53蛋白的活性。我们观察到在最后一剂2-氯脱氧腺苷后24小时采集的材料的上皮细胞中p53蛋白表达更强,这与细胞凋亡的活跃过程和增殖抑制有关。在最后一剂克拉屈滨给药4周后,p53蛋白的更强表达与细胞基因组的现有变化、正在进行的修复机制的影响以及高增殖活性有关。