The use of copper-lowering therapy with tetrathiomolybdate in medicine

被引:42
作者
Brewer, George J. [1 ,2 ]
机构
[1] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
关键词
alzheimer's disease therapy; anticopper therapy; autoimmune disease therapy; cancer therapy; fibrotic disease therapy; inflammatory disease therapy; tetrathiomolybdate; Wilson's disease therapy; NEUROLOGICALLY AFFECTED PATIENTS; PHASE-II TRIAL; SQUAMOUS-CELL CARCINOMA; AMMONIUM TETRATHIOMOLYBDATE; WILSONS-DISEASE; ALZHEIMERS-DISEASE; INITIAL THERAPY; MOUSE MODEL; FOLLOW-UP; PULMONARY-FIBROSIS;
D O I
10.1517/13543780802621859
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Background: Tetrathioimolybdate (TM), an anticopper drug, has been developed for the neurologic presentation of Wilson's disease. In animal models, lowering copper levels with TM produces antifibrotic, anti-inflammatory, antiautoimmune, and anticancer effects, thought to be due to inhibition of many cytokines that are dependent on available copper for their activity. Clinical testing has been done relatively extensively in Wilson's disease and advanced cancers, but remains in its infancy in other diseases. Objectives: To review current preclinical and clinical studies done with TM, and our current knowledge of TM efficacy and toxicity. Methods: We have reviewed the last 10 years of literature on TM therapy. Results/conclusion: TM has excellent efficacy and acceptable toxicity for the initial treatment of neurologically presenting Wilson's disease. TM has excellent efficacy in animal models of fibrotic, inflammatory, autoimmune, and neoplastic diseases, as well as Alzheimer's disease models.
引用
收藏
页码:89 / 97
页数:9
相关论文
共 72 条
[1]
Rapid restoration of cognition in Alzheimer's transgenic mice with 8-hydroxy quinoline analogs is associated with decreased interstitial Aβ [J].
Adlard, Paul A. ;
Cherny, Robert A. ;
Finkelstein, David I. ;
Gautier, Elisabeth ;
Robb, Elysia ;
Cortes, Mikhalina ;
Volitakis, Irene ;
Liu, Xiang ;
Smith, Jeffrey P. ;
Perez, Keyla ;
Laughton, Katrina ;
Li, Qiao-Xin ;
Charman, Susan A. ;
Nicolazzo, Joseph A. ;
Wilkins, Simon ;
Deleva, Karolina ;
Lynch, Toni ;
Kok, Gaik ;
Ritchie, Craig W. ;
Tanzi, Rudolph E. ;
Cappai, Roberto ;
Masters, Colin L. ;
Barnham, Kevin J. ;
Bush, Ashley I. .
NEURON, 2008, 59 (01) :43-55
[2]
BACE1 cytoplasmic domain interacts with the copper chaperone for superoxide dismutase-1 and binds copper [J].
Angeletti, B ;
Waldron, KJ ;
Freeman, KB ;
Bawagan, H ;
Hussain, I ;
Miller, CCJ ;
Lau, KF ;
Tennant, ME ;
Dennison, C ;
Robinson, NJ ;
Dingwall, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (18) :17930-17937
[3]
[Anonymous], HARRISONS PRINCIPLES
[4]
[Anonymous], 2001, WILSONS DIS CLIN GUI
[5]
Tetrathiomolybdate therapy protects against concanavalin A and carbon tetrachloride hepatic damage in mice [J].
Askari, FK ;
Dick, R ;
Mao, M ;
Brewer, GJ .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2004, 229 (08) :857-863
[6]
BIRK D, 2008, VASC ENDOVASCULAR SU
[7]
Thalidomide in multiple myeloma - clinical trials and aspects of drug metabolism and toxicity [J].
Breitkreutz, Iris ;
Anderson, Kenneth C. .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2008, 4 (07) :973-985
[8]
COPPER-METABOLISM IN RATS GIVEN DITHIOMOLYBDATES OR TRITHIOMOLYBDATES [J].
BREMNER, I ;
MILLS, CF ;
YOUNG, BW .
JOURNAL OF INORGANIC BIOCHEMISTRY, 1982, 16 (02) :109-119
[9]
TREATMENT OF WILSONS-DISEASE WITH AMMONIUM TETRATHIOMOLYBDATE .1. INITIAL THERAPY IN 17 NEUROLOGICALLY AFFECTED PATIENTS [J].
BREWER, G ;
DICK, RD ;
JOHNSON, V ;
WANG, YX ;
YUZBASIYANGURKAN, V ;
KLUIN, K ;
FINK, JK ;
AISEN, A .
ARCHIVES OF NEUROLOGY, 1994, 51 (06) :545-554
[10]
Brewer G.J., 2003, SEMIN INTEGR MED, V1, P181