Glucose conjugation for the specific targeting and treatment of cancer

被引:349
作者
Calvaresi, Emilia C. [1 ]
Hergenrother, Paul J. [1 ,2 ]
机构
[1] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Chem, Urbana, IL 61801 USA
基金
美国国家卫生研究院;
关键词
PHASE-II TRIAL; BIOLOGICAL EVALUATION; SUGAR-TRANSPORT; O-6-METHYLGUANINE-DNA METHYLTRANSFERASE; EUROPEAN ORGANIZATION; HUMAN-ERYTHROCYTES; ANTITUMOR-ACTIVITY; GLUT-1; EXPRESSION; 1-HOUR INFUSION; GENE-EXPRESSION;
D O I
10.1039/c3sc22205e
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Cancers of diverse origins exhibit marked glucose avidity and high rates of aerobic glycolysis. Increased understanding of this dysfunctional metabolism known as the Warburg effect has led to an interest in targeting it for cancer therapy. One promising strategy for such targeting is glycoconjugation, the linking of a drug to glucose or another sugar. This review summarizes the most salient examples of glycoconjugates, in which known cytotoxins or anticancer therapeutics have been linked to glucose (or another glucose transporter substrate sugar) for improved cancer targeting and selectivity. Building on these examples, this review also provides a series of guidelines for the design and mechanistic evaluation of future glycoconjugates.
引用
收藏
页码:2319 / 2333
页数:15
相关论文
共 99 条
[1]
Genes of glycolysis are ubiquitously overexpressed in 24 cancer classes [J].
Altenberg, B ;
Greulich, KO .
GENOMICS, 2004, 84 (06) :1014-1020
[2]
GLUT1 Expression Is Increased in Hepatocellular Carcinoma and Promotes Tumorigenesis [J].
Amann, Thomas ;
Maegdefrau, Ulrike ;
Hartmann, Arndt ;
Agaimy, Abbas ;
Marienhagen, Joerg ;
Weiss, Thomas S. ;
Stoeltzing, Oliver ;
Warnecke, Christina ;
Schoelmerich, Juergen ;
Oefner, Peter J. ;
Kreutz, Marina ;
Bosserhoff, Anja K. ;
Hellerbrand, Claus .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 174 (04) :1544-1552
[3]
Possible contribution of β-glucosidase and caspases in the cytotoxicity of glufosfamide in colon cancer cells [J].
Arafa, Hossam M. M. .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2009, 616 (1-3) :58-63
[4]
UNIQUE CYTOCHALASIN-B BINDING CHARACTERISTICS OF THE HEPATIC GLUCOSE CARRIER [J].
AXELROD, JD ;
PILCH, PF .
BIOCHEMISTRY, 1983, 22 (09) :2222-2227
[5]
STRUCTURAL REQUIREMENTS FOR BINDING TO SUGAR-TRANSPORT SYSTEM OF HUMAN ERYTHROCYTE [J].
BARNETT, JEG ;
HOLMAN, GD ;
MUNDAY, KA .
BIOCHEMICAL JOURNAL, 1973, 131 (02) :211-221
[6]
Measurement of sugar transport in single living cells [J].
Barros, LF .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1999, 437 (05) :763-770
[7]
18F-FDG PET and PET/CT in the Evaluation of Cancer Treatment Response [J].
Ben-Haim, Simona ;
Ell, Peter .
JOURNAL OF NUCLEAR MEDICINE, 2009, 50 (01) :88-99
[8]
New aspects of the Warburg effect in cancer cell biology [J].
Bensinger, Steven J. ;
Christofk, Heather R. .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2012, 23 (04) :352-361
[9]
Phase I trial of 6-hour infusion of glufosfamide, a new alkylating agent with potentially enhanced selectivity for tumors that overexpress transmembrane glucose transporters: A study of the European Organization for Research and Treatment of Cancer Early Clinical Studies Group [J].
Briasoulis, E ;
Judson, I ;
Pavlidis, N ;
Beale, P ;
Wanders, J ;
Groot, Y ;
Veerman, G ;
Schuessler, M ;
Niebch, G ;
Siamopoulos, K ;
Tzamakou, E ;
Rammou, D ;
Wolf, L ;
Walker, R ;
Hanauske, A .
JOURNAL OF CLINICAL ONCOLOGY, 2000, 18 (20) :3535-3544
[10]
Glufosfamide administered using a 1-hour infusion given as first-line treatment for advanced pancreatic cancer.: A phase II trial of the EORTC-new drug development group [J].
Briasoulis, E ;
Pavlidis, N ;
Terret, C ;
Bauer, J ;
Fiedler, W ;
Schöffski, P ;
Raoul, JL ;
Hess, D ;
Selvais, R ;
Lacombe, D ;
Bachmann, P ;
Fumoleau, P .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (16) :2334-2340