Alkynyl gold(I) phosphane complexes: Evaluation of structure-activity -relationships for the phosphane ligands, effects on key signaling proteins and preliminary in-vivo studies with a nanoformulated complex

被引:53
作者
Andermark, Vincent [1 ,2 ]
Goeke, Katrin [2 ,3 ]
Kokoschka, Malte [4 ,5 ]
Abu el Maaty, Mohamed A. [6 ]
Lum, Ching Tung [7 ,8 ]
Zou, Taotao [7 ,8 ]
Sun, Raymond Wai-Yin [7 ,8 ]
Aguilo, Elisabet [9 ]
Oehninger, Luciano [1 ,2 ]
Rodriguez, Laura [9 ]
Bunjes, Heike [2 ,3 ]
Woelfl, Stefan [6 ]
Che, Chi-Ming [7 ,8 ]
Ott, Ingo [1 ,2 ]
机构
[1] Tech Univ Carolo Wilhelmina Braunschweig, Inst Med & Pharmaceut Chem, Beethovenstr 55, D-38106 Braunschweig, Germany
[2] PVZ Ctr Pharmaceut Engn, Franz Liszt Str 35A, D-38106 Braunschweig, Germany
[3] Tech Univ Carolo Wilhelmina Braunschweig, Inst Pharmaceut Technol, Mendelssohnstr 1, D-38106 Braunschweig, Germany
[4] Acad Sci Czech Republ, Inst Organ Chem & Biochem, Gilead Sci & IOCB Res Ctr, Dept Computat Chem, Prague 16610 6, Czech Republic
[5] Palacky Univ, Dept Phys Chem, Olomouc 77146, Czech Republic
[6] Heidelberg Univ, Inst Pharm & Mol Biotechnol, Dept Biol, Neuenheimer Feld 364, D-69120 Heidelberg, Germany
[7] Univ Hong Kong, Chem Biol Ctr, State Key Lab Synthet Chem, 8-F Hong Kong Jockey Club Bldg Interdisciplinary, Hong Kong, Hong Kong, Peoples R China
[8] Univ Hong Kong, Dept Chem, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
[9] Univ Barcelona, Dept Quim Inorgan, Marti & Franques 1-11, E-08028 Barcelona, Spain
关键词
Alkyne; Cancer; Formulation; Gold; Microarray; Xenograft; THIOREDOXIN REDUCTASE INHIBITION; GENERALIZED GRADIENT APPROXIMATION; HETEROCYCLIC CARBENE COMPLEXES; ANTICANCER AGENTS; RATIONAL DESIGN; CANCER-CELLS; CHEMISTRY; CHEMOTHERAPEUTICS; PHARMACOLOGY; REACTIVITY;
D O I
10.1016/j.jinorgbio.2015.12.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gold alkynyl complexes with phosphane ligands of the type (alkynyl)Au(I)(phosphane) represent a group of bioorganometallics, which has only recently been evaluated biologically in more detail. Structure-activity-relationship studies regarding the residues of the phosphane ligand (P(Ph)(3), P(2-furyl)(3), P(DAPTA)(3), P(PTA)(3), P(Et)(3), P(Me)(3)) of complexes with an 4-ethynylanisole alkyne ligand revealed no strong differences concerning cytotoxicity. However, a relevant preference for the heteroatom free alkyl/aryl residues concerning inhibition of the target enzyme thioredoxin reductase was evident. Complex 1 with the triphenylphosphane ligand was selected for further studies, in which clear effects on cell morphology were monitored by time-lapse microscopy. Effects on cellular signaling were determined by ELISA microarrays and showed a significant induction of the phosphorylation of ERK1 (extracellular signal related kinase 1), ERK2 and HSP27 (heat shock protein 27) in HT-29 cells. Application of 1 in-vivo in a mouse xenograft model was found to be challenging due to the low solubility of the complex and required a formulation strategy based on a peanut oil nanoemulsion. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:140 / 148
页数:9
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