Targeting human telomerase for cancer therapeutics

被引:25
作者
Guittat, L
Alberti, P
Gomez, D
De Cian, A
Pennarun, G
Lemarteleur, T
Belmokhtar, C
Paterski, R
Morjani, H
Trentesaux, C
Mandine, E
Boussin, F
Mailliet, P
Lacroix, L
Riou, JF
Mergny, JL
机构
[1] Museum Natl Hist Nat, CNRS, INSERM,U565,UMR 5153, Biophys Lab, F-75231 Paris, France
[2] Univ Reims, UFR Pharm, Lab Oncopharmacol, F-51096 Reims, France
[3] CEA, Lab Radiopathol, F-92265 Fontenay Aux Roses, France
[4] Aventis Pharma SA, Ctr Rech Paris, F-94403 Vitry Sur Seine, France
关键词
apoptosis; cancer; G-quadruplex ligands; G-quartets; senescence; telomerase; telomere;
D O I
10.1007/s10616-004-5127-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The enzyme telomerase is involved in the replication of telomeres, specialized structures that cap and protect the ends of chromosomes. Its activity is required for maintenance of telomeres and for unlimited lifespan, a hallmark of cancer cells. Telomerase is overexpressed in the vast majority of human cancer cells and therefore represents an attractive target for therapy. Several approaches have been developed to inhibit this enzyme through the targeting of its RNA or catalytic components as well as its DNA substrate, the single-stranded 3'-telomeric overhang. Telomerase inhibitors are chemically diverse and include modified oligonucleotides as well as small diffusable molecules, both natural and synthetic. This review presents an update of recent investigations pertaining to these agents and discusses their biological properties in the context of the initial paradigm that the exposure of cancer cells to these agents should lead to progressive telomere shortening followed by a delayed growth arrest response.
引用
收藏
页码:75 / 90
页数:16
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