Most cited article - PubMed ID 17979756
Targeting of nuclear factor-kappaB and proteasome by dithiocarbamate complexes with metals
A series of three complexes with diethyldithiocarbamate ligand and three different metals (Ni, Cu, Zn) was prepared, confirmed by X-ray crystallography, and tested in human breast cancer MDA-MB-231 cells. Zinc and copper complexes, but not nickel complex, were found to be more active against cellular 26S proteasome than against purified 20S proteasome core particle. One of the possible explanations is inhibition of JAMM domain in the 19S proteasome lid.
- MeSH
- Ditiocarb analogs & derivatives chemistry pharmacology MeSH
- Enzyme Inhibitors chemistry pharmacology MeSH
- Proteasome Inhibitors * MeSH
- Humans MeSH
- Copper MeSH
- Molecular Structure MeSH
- Cell Line, Tumor MeSH
- Breast Neoplasms enzymology pathology MeSH
- Nickel MeSH
- Organometallic Compounds chemistry pharmacology MeSH
- Proteasome Endopeptidase Complex metabolism MeSH
- Zinc MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
- Names of Substances
- bis(N,N-diethyldithiocarbamate)Cu (II) complex MeSH Browser
- Ditiocarb MeSH
- Enzyme Inhibitors MeSH
- Proteasome Inhibitors * MeSH
- Copper MeSH
- Nickel MeSH
- Organometallic Compounds MeSH
- Proteasome Endopeptidase Complex MeSH
- Zinc MeSH