Journal
JOURNAL OF INORGANIC BIOCHEMISTRY
Volume 103, Issue 7, Pages 1082-1092Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2009.05.006
Keywords
Anticancer drug; Synthesis; DNA intercalators; Cytotoxicity; Crystal structure
Funding
- National Science Council, Taiwan
- Genomics Research Center Mass Spectrometry Facility
- Core Facility for Protein Production
- X-ray Structural Analysis in Academia Sinica
- Academia Sinica [NSC97-3112-B-001-017]
Ask authors/readers for more resources
Terpyridine-platinum(II) (TP-Pt(II)) complexes are known to possess DNA-intercalating activity and have been regarded as potential antitumor agents. However, their cytotoxic mechanism remains unclear. To investigate the possible mechanism, a series of TP-Pt(II) compounds were prepared and their biological activities assessed. The DNA binding activities of the aromatic thiolato[TP-Pt(II)] complexes were stronger than the aliphatic 2-hydroxylethanethiolato(2,2':6',2-terpyridine)platinum(II) [TP(HET)]. TP-Pt(II) complexes inhibited topoisomerase II alpha or topoisomerase I activity at IC50 values of about 5 mu M and 10-20 mu M, respectively, whereas the human thioredoxin reductase 1 (hTrxR1) activity was inhibited with IC50 values in the range of 58-78 nM. At the cellular level, they possessed cytotoxicity with IC50 values between 7 and 19 mu M against HeLa cells. Additionally, using X-ray crystallography and matrix-assisted laser desorption/ionization (MALDI) mass spectrometry, we elucidated that the TP-Pt(II) complexes inhibited hTrxR1 activity by blocking its C-terminal active-site selenocysteine. Therefore, TP-Pt(II) complexes possess inhibitory activities against multiple biological targets, and they may be further studied as anticancer agents. (C) 2009 Elsevier Inc. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available