Telomerase expression in lung preneoplasia and neoplasia

被引:65
作者
Lantuejoul, Sylvie
Salon, Caroline
Soria, Jean-Charles
Brambilla, Elisabeth
机构
[1] CHU Michallon, Inst A Bonniot, Dept Pathol, INSERM U 578, F-38043 Grenoble, France
[2] CHU Michallon, Inst A Bonniot, Lung Canc Res Grp, INSERM U 578, F-38043 Grenoble, France
[3] CEA, Lab Radiobiol & Oncol DSV DRR, Fontenay Aux Roses, France
关键词
telomerase; hTERT; lung cancer; preneoplasia;
D O I
10.1002/ijc.22473
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Telomeres are specialized structures at eukaryotic chromosomes ends, which role is to prevent them from degradation, end to-end fusion and rearrangement. However, they shorten after each cellular division because of an incomplete DNA replication, acting in normal somatic cells as a mitotic clock for permanent proliferation arrest or senescence entry. Short telomeres are perceived as damaged DNA leading to p53/ATM pathway activation. In tumoral cells, a ribonucleoprotein complex termed telomerase enables telomere elongation. This complex, composed of 2 main components, the telomerase RNA component or hTR, the RNA template for telomere synthesis, and telomerase reverse transcriptase, the catalytic subunit, is reactivated in the majority of cancers, including those of the lung. In this review, we briefly. present the main results on telomerase expression in various histological types or lung carcinoma and in bronchial carcinogenesis along with telomere attrition. Inhibition of one of the main components of the enzyme or limitation of telomere access by telomerase represent novel targets for cancer therapies and chemoprevention in high risk patients of lung cancer. (c) 2007 Wiley-Liss, Inc.
引用
收藏
页码:1835 / 1841
页数:7
相关论文
共 92 条
[1]  
Ahrendt SA, 1997, CLIN CANCER RES, V3, P1207
[2]   Telomerase activity in germ cell cancers and mature teratomas [J].
Albanell, J ;
Bosl, GJ ;
Reuter, VE ;
Engelhardt, M ;
Franco, S ;
Moore, MAS ;
Dmitrovsky, E .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (15) :1321-1326
[3]   High telomerase activity in primary lung cancers: Association with increased cell proliferation rates and advanced pathologic stage [J].
Albanell, J ;
Lonardo, F ;
Rusch, V ;
Engelhardt, M ;
Langenfeld, J ;
Han, W ;
Klimstra, D ;
Venkatraman, E ;
Moore, MAS ;
Dmitrovsky, E .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (21) :1609-1615
[4]   Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice [J].
Artandi, SE ;
Chang, S ;
Lee, SL ;
Alson, S ;
Gottlieb, GJ ;
Chin, L ;
DePinho, RA .
NATURE, 2000, 406 (6796) :641-645
[5]   Frequent recombination in telomeric DNA may extend the proliferative life of telomerase-negative cells [J].
Bailey, SM ;
Brenneman, MA ;
Goodwin, EH .
NUCLEIC ACIDS RESEARCH, 2004, 32 (12) :3743-3751
[6]   New developments in telomere length analysis [J].
Baird, DM .
EXPERIMENTAL GERONTOLOGY, 2005, 40 (05) :363-368
[7]   DNA damage response as a candidate anti-cancer barrier in early human tumorigenesis [J].
Bartkova, J ;
Horejsi, Z ;
Koed, K ;
Krämer, A ;
Tort, F ;
Zieger, K ;
Guldberg, P ;
Sehested, M ;
Nesland, JM ;
Lukas, C ;
Orntoft, T ;
Lukas, J ;
Bartek, J .
NATURE, 2005, 434 (7035) :864-870
[8]   Switching and signaling at the telomere [J].
Blackburn, EH .
CELL, 2001, 106 (06) :661-673
[9]   Extension of life-span by introduction of telomerase into normal human cells [J].
Bodnar, AG ;
Ouellette, M ;
Frolkis, M ;
Holt, SE ;
Chiu, CP ;
Morin, GB ;
Harley, CB ;
Shay, JW ;
Lichtsteiner, S ;
Wright, WE .
SCIENCE, 1998, 279 (5349) :349-352
[10]   TELOMERASE ACTIVITY IN NORMAL AND MALIGNANT HEMATOPOIETIC-CELLS [J].
BROCCOLI, D ;
YOUNG, JW ;
DELANGE, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (20) :9082-9086