Polyamines in cell growth and cell death: molecular mechanisms and therapeutic applications

被引:911
作者
Thomas, T
Thomas, TJ
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Environm & Community Med, New Brunswick, NJ 08903 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Med, New Brunswick, NJ 08903 USA
[3] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Environm & Occupat Hlth Sci Inst, New Brunswick, NJ 08903 USA
[4] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Canc Inst New Jersey, New Brunswick, NJ 08903 USA
关键词
polyamines; cell cycle; apoptosis; breast cancer;
D O I
10.1007/PL00000852
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Polyamines are aliphatic cations with multiple functions and are essential for life. Cellular polyamine levels are regulated by multiple pathways such as synthesis from amino acid precursors, cellular uptake mechanisms that salvage polyamines from diet and intestinal microorganisms, as well as stepwise degradation and efflux. Investigations using polyamine biosynthetic inhibitors indicate that alterations in cellular polyamine levels modulate normal and cancer cell growth. Studies using transgenic mice overexpressing polyamine biosynthetic enzymes support a role of polyamines in carcinogenesis. Many, if not all, signal transduction pathways intersect with polyamine biosynthetic pathways and the regulation of intracellular polyamine levels. Direct binding of polyamines to DNA and their ability to modulate DNA-protein interactions appear to be important in the molecular mechanisms of polyamine action in cell proliferation. Consistent with the role of polyamines as facilitators of cell growth, several studies have shown their ability to protect cells from apoptosis. However, polyamines also have a role in facilitating cell death. The basis of these diverse cellular responses is currently not known. Cell death response might be partly mediated by the production of hydrogen peroxide during polyamine catabolism. In addition, the ability of polyamines to alter DNA-protein and protein-protein interactions might be disruptive to cellular functions, when abnormally high levels are accumulated due to defects in polyamine catabolic or efflux pathways. A large body of data indicates that polyamine pathway can be a molecular target for therapeutic intervention in several types cancers. Inhibitors of biosynthesis, polyamine analogues as well as oligonucleotide/polyamine analogue combinations are promising drug candidates for chemoprevention and/or treatment of cancel.
引用
收藏
页码:244 / 258
页数:15
相关论文
共 172 条
[1]
Oligonucleotide therapeutics for hematologic disorders [J].
Agarwal, N ;
Gewirtz, AM .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 1999, 1489 (01) :85-96
[2]
Activation of polyamine catabolism in transgenic rats induces acute pancreatitis [J].
Alhonen, L ;
Parkkinen, JJ ;
Keinänen, T ;
Sinervirta, R ;
Herzig, KH ;
Jänne, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (15) :8290-8295
[3]
LIFELONG OVER-EXPRESSION OF ORNITHINE DECARBOXYLASE (ODC) GENE IN TRANSGENIC MICE DOES NOT LEAD TO GENERALLY ENHANCED TUMORIGENESIS OR NEURONAL DEGENERATION [J].
ALHONEN, L ;
HALMEKYTO, M ;
KOSMA, VM ;
WAHLFORS, J ;
KAUPPINEN, R ;
JANNE, J .
INTERNATIONAL JOURNAL OF CANCER, 1995, 63 (03) :402-404
[4]
Treatment of cells with the polyamine analog N1,N11-diethylnorspermine retards S phase progression within one cell cycle [J].
Alm, K ;
Berntsson, PSH ;
Kramer, DL ;
Porter, CW ;
Oredsson, SM .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (13) :4157-4164
[5]
CLOSING THE CELL-CYCLE CIRCLE IN YEAST - G2 CYCLIN PROTEOLYSIS INITIATED AT MITOSIS PERSISTS UNTIL THE ACTIVATION OF G1 CYCLINS IN THE NEXT CYCLE [J].
AMON, A ;
IRNIGER, S ;
NASMYTH, K .
CELL, 1994, 77 (07) :1037-1050
[6]
Auvinen M, 1997, CANCER RES, V57, P3016
[7]
DNA LOOPS INDUCED BY COOPERATIVE BINDING OF TRANSCRIPTIONAL ACTIVATOR PROTEINS AND PREINITIATION COMPLEXES [J].
BECKER, JC ;
NIKROO, A ;
BRABLETZ, T ;
REISFELD, RA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (21) :9727-9731
[8]
EFFECTS OF METHYLATION ON A SYNTHETIC POLYNUCLEOTIDE - THE B-Z TRANSITION IN POLY(DG-M5DC).POLY(DG-M5DC) [J].
BEHE, M ;
FELSENFELD, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (03) :1619-1623
[9]
THE ORNITHINE DECARBOXYLASE GENE IS A TRANSCRIPTIONAL TARGET OF C-MYC [J].
BELLOFERNANDEZ, C ;
PACKHAM, G ;
CLEVELAND, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (16) :7804-7808
[10]
Bernacki RJ, 1995, CLIN CANCER RES, V1, P847