Mimic catechins to develop selective MMP-2 inhibitors

被引:4
作者
Di Pizio, Antonella [1 ]
Agamennone, Mariangela [2 ]
Laghezza, Antonio [3 ]
Loiodice, Fulvio [3 ]
Tortorella, Paolo [3 ]
机构
[1] Hebrew Univ Jerusalem, Inst Biochem Food Sci & Nutr, Robert H Smith Fac Agr Food & Environm, Rehovot, Israel
[2] Univ G dAnnunzio, Dipartimento Farm, Chieti, Italy
[3] Univ A Moro Bari, Dipartimento Farm Sci Farmaco, Bari, Italy
来源
MONATSHEFTE FUR CHEMIE | 2018年 / 149卷 / 07期
关键词
Enzymes; Ligands; Molecular modelling; Flavonoids; MMP inhibitors; Anticancer drugs; MATRIX-METALLOPROTEINASE INHIBITORS; HYDROXAMATE INHIBITOR; ACTIVE-SITE; CANCER; WATER; IDENTIFICATION; PATHWAYS; BIOLOGY; DESIGN; CELLS;
D O I
10.1007/s00706-018-2237-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Matrix metalloproteinase 2 (MMP-2) is a well-known anticancer target belonging to the MMP family. Because of the bilateral role of MMPs in cancer, developing highly selective MMP-2 inhibitors is a current challenge. In this paper, we investigated the binding modes of green tea polyphenols epigallocatechin gallate and epicatechin into the active site of the MMP-2 enzyme. The structure-based analysis allowed the optimization of these hits and hence led to a better lead candidate. Moreover, using a pharmacophore model, we screened FooDB compounds and selected food components as potential MMP-2 inhibitors. The search for food-derived compounds that target this enzyme may represent a strategy to identify new lead molecules with improved safety profiles and provide indications about possible functional foods. [GRAPHICS] .
引用
收藏
页码:1293 / 1300
页数:8
相关论文
共 43 条
[1]   Zinc-binding groups modulate selective inhibition of MMPs [J].
Agrawal, Arpita ;
Romero-Perez, Diego ;
Jacobsen, Jennifer A. ;
Villarreal, Francisco J. ;
Cohen, Seth M. .
CHEMMEDCHEM, 2008, 3 (05) :812-820
[2]   Loss of collagenase-2 confers increased skin tumor susceptibility to male mice [J].
Balbín, M ;
Fueyo, A ;
Tester, AM ;
Pendás, AM ;
Pitiot, AS ;
Astudillo, A ;
Overall, CM ;
Shapiro, SD ;
López-Otín, C .
NATURE GENETICS, 2003, 35 (03) :252-257
[3]   Water as an active constituent in cell biology [J].
Ball, Philip .
CHEMICAL REVIEWS, 2008, 108 (01) :74-108
[5]   Snapshots of the reaction mechanism of matrix metalloproteinases [J].
Bertini, Ivano ;
Calderone, Vito ;
Fragai, Marco ;
Luchinat, Claudio ;
Maletta, Massimiliano ;
Yeo, Kwon Joo .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (47) :7952-7955
[6]   Shedding Light on Important Waters for Drug Design: Simulations versus Grid-Based Methods [J].
Bucher, Denis ;
Stouten, Pieter ;
Triballeau, Nicolas .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2018, 58 (03) :692-699
[7]   Inhibition of pro-/active MMP-2 by green tea catechins and prediction of their interaction by molecular docking studies [J].
Chowdhury, Animesh ;
Nandy, Suman Kumar ;
Sarkar, Jaganmay ;
Chakraborti, Tapati ;
Chakraborti, Sajal .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 2017, 427 (1-2) :111-122
[8]   In silico identification of anti-cancer compounds and plants from traditional Chinese medicine database [J].
Dai, Shao-Xing ;
Li, Wen-Xing ;
Han, Fei-Fei ;
Guo, Yi-Cheng ;
Zheng, Jun-Juan ;
Liu, Jia-Qian ;
Wang, Qian ;
Gao, Yue-Dong ;
Li, Gong-Hua ;
Huang, Jing-Fei .
SCIENTIFIC REPORTS, 2016, 6
[9]   Solvent water interactions within the active site of the membrane type I matrix metalloproteinase [J].
Decaneto, Elena ;
Vasilevskaya, Tatiana ;
Kutin, Yuri ;
Ogata, Hideaki ;
Grossman, Moran ;
Sagi, Irit ;
Havenith, Martina ;
Lubitz, Wolfgang ;
Thiel, Walter ;
Cox, Nicholas .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2017, 19 (45) :30316-30331
[10]   A structure-activity study for the inhibition of metalloproteinase-9 activity and gene expression by analogues of gallocatechin-3-gallate [J].
Dell'Agli, M ;
Bellosta, S ;
Rizzi, L ;
Galli, G ;
Canavesi, M ;
Rota, F ;
Parente, R ;
Bosisio, E ;
Romeo, S .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (23) :2896-2903