Acilan Ceyda, Cevatemre Buse, Adiguzel Zelal, Karakas Didem, Ulukaya Engin, Ribeiro Nádia, Correia Isabel, Pessoa João Costa
TUBITAK, Marmara Research Center, Genetic Engineering and Biotechnology Institute, Gebze, Kocaeli, Turkey.
Uludag University, Faculty of Arts and Sciences, Department of Biology, Bursa, Turkey.
Data Brief. 2016 Nov 22;9:1160-1174. doi: 10.1016/j.dib.2016.11.063. eCollection 2016 Dec.
Three copper(II) complexes, Cu(Sal-Gly)(phen), Cu(Sal-Gly)pheamine, Cu(Sal-Gly)phepoxy were synthesized and characterized for their anticancer properties and mechanism of action (Acilan et al., in press) [1]. Here, we provide supporting data on colon cancer cell lines complementing our previous findings in cervix cells. This paper also contains a data table for the fold changes and -values of all genes analyzed in this study via a custom RT-qPCR array. All compounds induced DNA damage (based on 8-oxo-guanidine, ɣH2AX staining in cells) and apoptosis (based on elevated DNA condensation/fragmentation, Annexin V staining, caspase 3/7 activity and mitochondrial membrane depolarization) in HCT-116 colon cancer cells. The increase in oxidative stress was also further confirmed in these cells. Further interpretation of the data presented here can be found in the article entitled "Synthesis, biological characterization and evaluation of molecular mechanisms of novel copper complexes as anticancer agents" (Acilan et al., in press) [1].
合成了三种铜(II)配合物,即Cu(Sal-Gly)(phen)、Cu(Sal-Gly)pheamine、Cu(Sal-Gly)phepoxy,并对其抗癌特性和作用机制进行了表征(阿西兰等人,即将发表)[1]。在此,我们提供了关于结肠癌细胞系的支持数据,以补充我们之前在宫颈细胞中的研究结果。本文还包含一个数据表,列出了通过定制的逆转录定量聚合酶链反应(RT-qPCR)阵列分析的本研究中所有基因的倍数变化和P值。所有化合物均在HCT-116结肠癌细胞中诱导了DNA损伤(基于细胞中的8-氧代鸟嘌呤、ɣH2AX染色)和细胞凋亡(基于DNA浓缩/片段化增加、膜联蛋白V染色、半胱天冬酶3/7活性和线粒体膜去极化)。这些细胞中氧化应激的增加也得到了进一步证实。本文所呈现数据的进一步解读可在题为《新型铜配合物作为抗癌剂的合成、生物学表征及分子机制评估》的文章中找到(阿西兰等人,即将发表)[1]。