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Over-expression of nm23-H1 in HeLa cells provides cells with higher resistance to oxidative stress possibly due to raising intracellular p53 and GPX1.
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- معلومة اضافية
- المصدر:
Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 100956087 Publication Model: Print Cited Medium: Internet ISSN: 1745-7254 (Electronic) Linking ISSN: 16714083 NLM ISO Abbreviation: Acta Pharmacol Sin Subsets: MEDLINE
- بيانات النشر:
Publication: 2009- : New York : Nature Publishing Group
Original Publication: Beijing, China : Science Press, c2000-
- الموضوع:
- نبذة مختصرة :
Aim: To determine whether the antitumor factor nm23 is related with antioxidation.
Methods: Full-length human nm23-H1 was cloned into a mammalianexpressing vector and transiently introduced into HeLa cells.
Results: A remarkably low level of reactive oxygen species (ROS) was detected in the cells overexpressing nm23-H1. 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and trypan blue assays found that the cells transfected with a nm23- H1-expressing plasmid had higher viability and stronger resistance to oxidative stress. Immunoprecipitation tests revealed that endogenous nm23-H1 formed a protein complex with p53. Furthermore, the intracellular levels of p53 and p53- regulated gene GPX1 were obviously increased in the cells overexpressing nm23- H1. The downregulation of p53 in the cells overexpressing nm23-H1 resulted in a higher cellular ROS level and lower cell viability.
Conclusion: The findings suggest that nm23-H1 may act as a cellular protector against oxidative stress, possibly triggering the p53-related antioxidative pathway.
- الرقم المعرف:
0 (NM23 Nucleoside Diphosphate Kinases)
0 (Oxidants)
0 (Reactive Oxygen Species)
0 (Tumor Suppressor Protein p53)
BBX060AN9V (Hydrogen Peroxide)
EC 1.11.1.9 (Glutathione Peroxidase)
EC 2.7.4.6 (NME1 protein, human)
EC 1.11.1.9 (Glutathione Peroxidase GPX1)
EC 1.11.1.9 (GPX1 protein, human)
- الموضوع:
Date Created: 20081126 Date Completed: 20090417 Latest Revision: 20221207
- الموضوع:
20240829
- الرقم المعرف:
10.1111/j.1745-7254.2008.00902.x
- الرقم المعرف:
19026164
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