Gold(I) complexes of 9-deazahypoxanthine as selective antitumor and anti-inflammatory agents
Language English Country United States Media electronic-ecollection
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25333949
PubMed Central
PMC4198181
DOI
10.1371/journal.pone.0109901
PII: PONE-D-14-31451
Knihovny.cz E-resources
- MeSH
- Anti-Inflammatory Agents chemistry pharmacology therapeutic use MeSH
- Edema drug therapy MeSH
- Hepatocytes drug effects MeSH
- Hypoxanthines chemistry pharmacology therapeutic use MeSH
- Rats MeSH
- Humans MeSH
- Disease Models, Animal MeSH
- Cell Line, Tumor MeSH
- Neoplasms drug therapy MeSH
- Antineoplastic Agents chemistry pharmacology therapeutic use MeSH
- Spectroscopy, Fourier Transform Infrared MeSH
- Inflammation drug therapy MeSH
- Gold chemistry pharmacology therapeutic use MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Humans MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 9-deazahypoxanthine MeSH Browser
- Anti-Inflammatory Agents MeSH
- Hypoxanthines MeSH
- Antineoplastic Agents MeSH
- Gold MeSH
The gold(I) mixed-ligand complexes involving O-substituted derivatives of 9-deazahypoxanthine (HLn) and triphenylphosphine (PPh3) with the general formula [Au(Ln)(PPh3)] (1-5) were prepared and thoroughly characterized by elemental analysis, FT-IR and multinuclear NMR spectroscopy, ESI+ mass spectrometry, single crystal X-ray (HL5 and complex 2) and TG/DTA analyses. Complexes 1-5 were evaluated for their in vitro antitumor activity against nine human cancer lines, i.e. MCF7 (breast carcinoma), HOS (osteosarcoma), A549 (adenocarcinoma), G361 (melanoma), HeLa (cervical cancer), A2780 (ovarian carcinoma), A2780R (ovarian carcinoma resistant to cisplatin), 22Rv1 (prostate cancer) and THP-1 (monocytic leukaemia), for their in vitro anti-inflammatory activity using a model of LPS-activated macrophages, and for their in vivo antiedematous activity by λ-carrageenan-induced hind paw edema model on rats. The results showed that the complexes 1-5 exhibit selective in vitro cytotoxicity against MCF7, HOS, 22Rv1, A2780 and A2780R, with submicromolar IC50 values for 2 against the MCF7 (0.6 µM) and HOS (0.9 µM). The results of in vitro cytotoxicity screening on primary culture of human hepatocytes (HEP220) revealed up to 30-times lower toxicity of compounds against healthy cells as compared with cancer cells. Additionally, the complexes 1-5 significantly influence the secretion and expression of pro-inflammatory cytokines TNF-α and IL-1β by a similar manner as a commercially used anti-arthritic drug Auranofin. The tested complexes also significantly influence the rate and overall volume of the edema, caused by the intraplantar application of λ-carrageenan polysaccharide to rats. Based on these promising results, the presented compounds could qualify to become feasible candidates for advanced testing as potential antitumor and anti-inflammatory drug-like compounds.
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In Vitro Antitumor Active Gold(I) Triphenylphosphane Complexes Containing 7-Azaindoles