Recent advances in MMP inhibitor design

被引:211
作者
Fisher, JF [1 ]
Mobashery, S [1 ]
机构
[1] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
matrix metalloprotease; metalloproteinase gelatinase; collagenase;
D O I
10.1007/s10555-006-7894-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The search for an MMP inhibitor with anticancer efficacy is a nearly three-decade endeavor. This inhibitor is yet to be found. The reasons for this failure include shortcomings in the chemistry of these compounds (including broad MMP sub-type selectivity, metabolic lability, and toxicity) as well as the emerging, and arguably extraordinary, complexity of MMP cell (and cancer) biology. Together these suggest that the successful anticancer inhibitor must possess MMP selectivity against the MMP subtype whose involvement is critical, yet highly temporally (with respect to metastatic progression) and mechanistically (with respect to matrix degradation) regulated. This review summarizes the progression of chemical structure and mechanistic thinking toward these objectives, with emphasis on the disappointment, the perseverance, and the resilient optimism that such an inhibitor is there to be discovered.
引用
收藏
页码:115 / 136
页数:22
相关论文
共 230 条
[1]   Chemically modified tetracyclines as inhibitors of matrix metalloproteinases [J].
Acharya, MR ;
Venitz, E ;
Figg, WD ;
Sparreboom, A .
DRUG RESISTANCE UPDATES, 2004, 7 (03) :195-208
[2]   Synthesis and evaluation of new tripeptide phosphonate inhibitors of MMP-8 and MMP-2 [J].
Agamennone, M ;
Campestre, C ;
Preziuso, S ;
Consalvi, V ;
Crucianelli, M ;
Mazza, F ;
Politi, V ;
Ragno, R ;
Tortorella, P ;
Gallina, C .
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2005, 40 (03) :271-279
[3]   Stromelysin-3 is a potent negative regulator of adipogenesis participating to cancer cell-adipocyte interaction/crosstalk at the tumor invasive front [J].
Andarawewa, KL ;
Motrescu, ER ;
Chenard, MP ;
Gansmuller, A ;
Stoll, I ;
Tomasetto, C ;
Rio, MC .
CANCER RESEARCH, 2005, 65 (23) :10862-10871
[4]  
Andarawewa KL, 2003, CANCER RES, V63, P5844
[5]   Counting the zinc-proteins encoded in the human genome [J].
Andreini, C ;
Banci, L ;
Bertini, I ;
Rosato, A .
JOURNAL OF PROTEOME RESEARCH, 2006, 5 (01) :196-201
[6]   Synthesis and structure-activity relationship of α-sulfonylhydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritis [J].
Aranapakam, V ;
Grosu, GT ;
Davis, JM ;
Hu, BH ;
Ellingboe, J ;
Baker, JL ;
Skotnicki, JS ;
Zask, A ;
DiJoseph, JF ;
Sung, A ;
Sharr, MA ;
Killar, LM ;
Walter, T ;
Jin, GX ;
Cowling, R .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (12) :2361-2375
[7]   Synthesis and structure-activity relationship of N-substituted 4-arylsulfonylpiperidine-4-hydroxamic acids as novel, orally active matrix metalloproteinase inhibitors for the treatment of osteoarthritis [J].
Aranapakam, V ;
Davis, JM ;
Grosu, GT ;
Baker, J ;
Ellingboe, J ;
Zask, A ;
Levin, JI ;
Sandanayaka, VP ;
Du, ML ;
Skotnicki, JS ;
DiJoseph, JF ;
Sung, A ;
Sharr, MA ;
Killar, LM ;
Walter, T ;
Jin, GX ;
Cowling, R ;
Tillett, J ;
Zhao, WU ;
McDevitt, J ;
Xu, ZB .
JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (12) :2376-2396
[8]  
ARLT M, 2001, CLIN CANCER RES, V7, P1912
[9]   Synthesis and structure-activity relationships of β- and α-piperidine sulfone hydroxamic acid matrix metalloproteinase inhibitors with oral antitumor efficacy [J].
Becker, DP ;
Villamil, CI ;
Barta, TE ;
Bedell, LJ ;
Boehm, TL ;
DeCrescenzo, GA ;
Freskos, JN ;
Getman, DP ;
Hockerman, S ;
Heintz, R ;
Howard, SC ;
Li, MH ;
McDonald, JJ ;
Carron, CP ;
Funckes-Shippy, CL ;
Mehta, PP ;
Munie, GE ;
Swearingen, CA .
JOURNAL OF MEDICINAL CHEMISTRY, 2005, 48 (21) :6713-6730
[10]  
Béliveau R, 2002, CLIN CANCER RES, V8, P1242