Divergent patterns of telomere maintenance mechanisms among human sarcomas: Sharply contrasting prevalence of the alternative lengthening of telomeres mechanism in Ewing's sarcomas and osteosarcomas

被引:71
作者
Ulaner, GA
Hoffman, AR
Otero, J
Huang, HY
Zhao, ZQ
Mazumdar, M
Gorlick, R
Meyers, P
Healey, JH
Ladanyi, M
机构
[1] VA Palo Alto Hlth Care Syst, Med Serv, Palo Alto, CA 94304 USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[3] Stanford Univ, Dept Med, Palo Alto, CA 94304 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Pathol, New York, NY 10021 USA
[5] Mem Sloan Kettering Canc Ctr, Dept Epidemiol & Biostat, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Pediat, New York, NY 10021 USA
[7] Mem Sloan Kettering Canc Ctr, Dept Orthopaed Surg, New York, NY 10021 USA
关键词
D O I
10.1002/gcc.20074
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Two types of telomere maintenance mechanisms (TMMs) have been described in human tumors: telomerase activation and alternative lengthening of telomeres (ALT). Although the vast majority of epithelial tumors rely on telomerase activation, many mesenchymal tumors rely on ALT for telomere maintenance, but within this tumor group, the TMMs used by translocation-associated sarcomas have not been systematically studied. We studied telomere lengths and telomerase expression and activity in 30 uncultured tumor samples and in 10 cell lines of Ewing's sarcoma, a prototypical translocation-associated sarcoma, and compared the data to an identical analysis of 60 osteosarcomas, the most common type of sarcoma lacking a specific translocation. Telomerase activity was demonstrated in 21 Ewing's sarcoma tumor samples (70%) and in 9 of 10 Ewing's sarcoma cell lines. Evidence of ALT, indicated by the presence of long and heterogeneous telomeres, was observed only in the cell line without telomerase activity and in none of the 30 Ewing's sarcoma tumor samples. The 9 Ewing's sarcoma patients whose tumors lacked detectable telomerase activity did not differ significantly from the remaining patients in age, stage, EWSR1-FLI1 fusion type, prevalence of TP53 point mutations, or overall survival. The low prevalence of ALT in Ewing's sarcoma contrasted sharply with our data on TMMs in 60 osteosarcomas, which showed ALT in 38 of 60 cases (P < 0.0001). The present study, together with emerging published data on other sarcoma types, suggests that a predominance of telomerase activation in the absence of ALT may characterize sarcomas with specific chromosomal translocations (such as Ewing's sarcoma), whereas a high prevalence of ALT appears typical of sarcomas with nonspecific complex karyotypes (such as osteosarcoma). (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:155 / 162
页数:8
相关论文
共 42 条
[1]   Translocations, cancer and the puzzle of specificity [J].
Barr, FG .
NATURE GENETICS, 1998, 19 (02) :121-124
[2]  
Borden EC, 2003, CLIN CANCER RES, V9, P1941
[3]   Human POT1 facilitates telomere elongation by telomerase [J].
Colgin, LM ;
Baran, K ;
Baumann, P ;
Cech, TR ;
Reddel, RR .
CURRENT BIOLOGY, 2003, 13 (11) :942-946
[4]   Analysis of the expression of cell cycle regulators in Ewing cell lines:: EWS-FLI-1 modulates p57KIP2 and c-Myc expression [J].
Dauphinot, L ;
De Oliveira, C ;
Melot, T ;
Sevenet, N ;
Thomas, V ;
Weissman, BE ;
Delattre, O .
ONCOGENE, 2001, 20 (25) :3258-3265
[5]   GENE FUSION WITH AN ETS DNA-BINDING DOMAIN CAUSED BY CHROMOSOME-TRANSLOCATION IN HUMAN TUMORS [J].
DELATTRE, O ;
ZUCMAN, J ;
PLOUGASTEL, B ;
DESMAZE, C ;
MELOT, T ;
PETER, M ;
KOVAR, H ;
JOUBERT, I ;
DEJONG, P ;
ROULEAU, G ;
AURIAS, A ;
THOMAS, G .
NATURE, 1992, 359 (6391) :162-165
[6]   Upregulation of Id2, an oncogenic helix-loop-helix protein, is mediated by the chimeric EWS/ets protein in Ewing sarcoma [J].
Fukuma, M ;
Okita, H ;
Hata, J ;
Umezawa, A .
ONCOGENE, 2003, 22 (01) :1-9
[7]  
Gisselsson D, 2002, HISTOL HISTOPATHOL, V17, P1207, DOI 10.14670/HH-17.1207
[8]   Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity [J].
Gisselsson, D ;
Pettersson, L ;
Höglund, M ;
Heidenblad, M ;
Gorunova, L ;
Wiegant, J ;
Mertens, F ;
Dal Cin, P ;
Mitelman, F ;
Mandahl, N .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (10) :5357-5362
[9]   Short telomeres result in organismal hypersensitivity to ionizing radiation in mammals [J].
Goytisolo, FA ;
Samper, E ;
Martín-Caballero, J ;
Finnon, P ;
Herrera, E ;
Flores, JM ;
Bouffler, SD ;
Blasco, MA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (11) :1625-1636
[10]   Is telomerase activity in cancer due to selection of stem cells and differentiation arrest? [J].
Greaves, M .
TRENDS IN GENETICS, 1996, 12 (04) :127-128