Zinc-Doped Copper Oxide Nanocomposites Inhibit the Growth of Human Cancer Cells through Reactive Oxygen Species-Mediated NF-κB Activations

2016 ◽  
Vol 8 (46) ◽  
pp. 31806-31812 ◽  
Author(s):  
Ru Yuan ◽  
Huanli Xu ◽  
Xiaohui Liu ◽  
Ye Tian ◽  
Cong Li ◽  
...  
Keyword(s):  
Reactive Oxygen Species ◽  
Copper Oxide ◽  
Cancer Cells ◽  
Human Cancer ◽  
Reactive Oxygen ◽  
Oxygen Species ◽  
Human Cancer Cells

scholarly journals The Anticancer Drug 3-Bromopyruvate Induces DNA Damage Potentially Through Reactive Oxygen Species in Yeast and in Human Cancer Cells

Cells ◽  
2020 ◽  
Vol 9 (5) ◽  
pp. 1161 ◽  
Author(s):  
Magdalena Cal ◽  
Irwin Matyjaszczyk ◽  
Ireneusz Litwin ◽  
Daria Augustyniak ◽  
Rafał Ogórek ◽  
...  
Keyword(s):  
Reactive Oxygen Species ◽  
Dna Damage ◽  
Cancer Cells ◽  
Human Cancer ◽  
Reactive Oxygen ◽  
Atp Depletion ◽  
Mitochondrial Enzymes ◽  
Oxygen Species ◽  
Human Cancer Cells ◽  
The Impact

3-bromopyruvate (3-BP) is a small molecule with anticancer and antimicrobial activities. 3-BP is taken up selectively by cancer cells’ mono-carboxylate transporters (MCTs), which are highly overexpressed by many cancers. When 3-BP enters cancer cells it inactivates several glycolytic and mitochondrial enzymes, leading to ATP depletion and the generation of reactive oxygen species. While mechanisms of 3-BP uptake and its influence on cell metabolism are well understood, the impact of 3-BP at certain concentrations on DNA integrity has never been investigated in detail. Here we have collected several lines of evidence suggesting that 3-BP induces DNA damage probably as a result of ROS generation, in both yeast and human cancer cells, when its concentration is sufficiently low and most cells are still viable. We also demonstrate that in yeast 3-BP treatment leads to generation of DNA double-strand breaks only in S-phase of the cell cycle, possibly as a result of oxidative DNA damage. This leads to DNA damage, checkpoint activation and focal accumulation of the DNA response proteins. Interestingly, in human cancer cells exposure to 3-BP also induces DNA breaks that trigger H2A.X phosphorylation. Our current data shed new light on the mechanisms by which a sufficiently low concentration of 3-BP can induce cytotoxicity at the DNA level, a finding that might be important for the future design of anticancer therapies.

scholarly journals Aescin-induced reactive oxygen species play a pro-survival role in human cancer cells via ATM/AMPK/ULK1-mediated autophagy

2018 ◽  
Vol 39 (12) ◽  
pp. 1874-1884 ◽  
Author(s):  
Bin Li ◽  
Guo-liang Wu ◽  
Wei Dai ◽  
Gang Wang ◽  
Hao-yuan Su ◽  
...  
Keyword(s):  
Reactive Oxygen Species ◽  
Cancer Cells ◽  
Human Cancer ◽  
Reactive Oxygen ◽  
Oxygen Species ◽  
Human Cancer Cells

scholarly journals Farnesyltransferase Inhibitors Induce DNA Damage via Reactive Oxygen Species in Human Cancer Cells

2005 ◽  
Vol 65 (9) ◽  
pp. 3671-3681 ◽  
Author(s):  
Jingxuan Pan ◽  
Miaorong She ◽  
Zhi-Xiang Xu ◽  
Lily Sun ◽  
Sai-Ching Jim Yeung
Keyword(s):  
Reactive Oxygen Species ◽  
Dna Damage ◽  
Cancer Cells ◽  
Human Cancer ◽  
Reactive Oxygen ◽  
Oxygen Species ◽  
Farnesyltransferase Inhibitors ◽  
Human Cancer Cells
Sign in / Sign up

Export Citation Format

Share Document