Details

Autor(en) / Beteiligte

• Hille, Annegret
• Wolf, Tanja
• Schumacher, Petra
• Ott, Ingo
• Gust, Ronald
• Kircher, Brigitte

Titel

Effects of Metal Salophene and Saldach Complexes on Lymphoma and Leukemia Cells

Ist Teil von

• Archiv der Pharmazie (Weinheim), 2011-04, Vol.344 (4), p.217-223

Ort / Verlag

Weinheim: WILEY-VCH Verlag

Erscheinungsjahr

2011

Link zum Volltext

Quelle

Wiley Blackwell Single Titles

Beschreibungen/Notizen

• Schiff base transition metal complexes are an important class of compounds with great potential for therapeutic interventions. However, data on antileukemic and antilymphoma effects of these complexes are limited. The activity of N,N′‐bis(salicylidene)‐1,2‐phenylenediamine (salophene, 1), its iron(II/III) and manganese(II/III) complexes as well as rac‐trans‐N,N′‐bis(salicylidene)‐1,2‐cyclohexanediamine (saldach, 2) and its respective iron(II/III) complexes was evaluated against U‐937 non‐Hodgkin's lymphoma and the HL‐60, SUP‐B15, and K‐562 leukemia cell lines. The free ligands induced in all cell lines, if at all, only marginal, concentration‐dependent growth inhibitory effects, and did not trigger Cu/Zn superoxide dismutase (Cu/Zn SOD) release or induce apoptosis. [FeII(salophene)] (3) and [FeIII(salophene)Cl] (4) blocked cellular growth, caused a strong release of Cu/Zn SOD and induced apoptosis. In contrast, the manganese analogs [MnII(salophene)] (5) and [MnIII(salophene)OAc] (6) inhibited cell growth, caused the programmed cell death only at higher concentrations and did not provoke release of Cu/Zn SOD in any of the four cell lines. Weaker cell death‐promoting effects were observed when the salophene moiety of 3 and 4 was replaced with saldach (complexes 7 and 8), indicating the influence exerted by the ligand structure. In conclusion, Schiff base transition metal complexes induce strong inhibitory effects on human lymphoma and leukemia cells. Similar but still different – dependent on the transition metal and the ligand structure: Iron salophene and saldach complexes induce various cellular changes such as inhibition of cell growth, induction of apoptosis and release of Cu/Zn superoxide dismutase, a cellular repair enzyme, in human lymphoma and leukemia cell lines. Manganese salophene complexes inhibit only cell growth and free ligands are almost ineffective.