Anticancer activity studies of a ruthenium(II) polypyridyl complex against human hepatocellular (BEL-7402) cells

التفاصيل البيبلوغرافية
العنوان: Anticancer activity studies of a ruthenium(II) polypyridyl complex against human hepatocellular (BEL-7402) cells
المؤلفون: Yun-Jun Liu, Hong-Liang Huang, Jun-Hua Yao, Wei Li, Gan-Jian Lin, Yang-Yin Xie, Guang-Bin Jiang, Bing-Jie Han
المصدر: Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 150:127-134
بيانات النشر: Elsevier BV, 2015.
سنة النشر: 2015
مصطلحات موضوعية: Cell, chemistry.chemical_element, Antineoplastic Agents, Apoptosis, Analytical Chemistry, 2,2'-Dipyridyl, Cell Line, Tumor, Organometallic Compounds, medicine, Humans, Cytotoxic T cell, Instrumentation, Spectroscopy, Membrane Potential, Mitochondrial, Membrane potential, chemistry.chemical_classification, Reactive oxygen species, Cell growth, Chemistry, Liver Neoplasms, Cell Cycle Checkpoints, Molecular biology, Atomic and Molecular Physics, and Optics, Ruthenium, medicine.anatomical_structure, Liver, Cancer cell, Reactive Oxygen Species
الوصف: A Ru(II) polypyridyl complex [Ru(bpy)2(HMSPIP)](ClO4)2 (1) (bpy=2,2'-bipyridine, HMSPIP=2-(4-methylsulfonyl)phenyl-1H-imidazo[4,5-f][1,10] phenanthroline) was synthesized. The IC50 value of the complex against human hepatocellular cell BEL-7402 is 21.6±2.7 μM. The complex shows no cytotoxic activity toward human lung adenocarcinoma cell A549, human osteosarcoma cell MG-63 and human breast cancer cell SK-BR-3 cells. It is easily for complex 1 to be taken up by BEL-7402 cells. The complex can enhance the reactive oxygen species (ROS) levels and induce the decrease in the mitochondrial membrane potential. The complex inhibits the cell growth in BEL-7402 cells at G2/M phase. Complex 1 can regulate the expression of Bcl-2 family proteins. The results show that the complex induces apoptosis of BEL-7402 cells through a ROS-mediated mitochondrial dysfunction pathway.
تدمد: 1386-1425
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a78320b0762dcd978a885b5fa64ebf6
https://doi.org/10.1016/j.saa.2015.05.032
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....7a78320b0762dcd978a885b5fa64ebf6
قاعدة البيانات: OpenAIRE