Tumour specific regulation of telomerase RNA gene expression visualized by in situ hybridization

被引:70
作者
Soder, AI
Going, JJ
Kaye, SB
Keith, WN
机构
[1] Univ Glasgow, CRC, Beatson Labs, Dept Med Oncol, Glasgow G61 1BD, Lanark, Scotland
[2] Glasgow Royal Infirm, Dept Pathol, Glasgow G4 0SF, Lanark, Scotland
关键词
telomerase; in situ hybridization; gene expression; hTR; ribonucleoproteins;
D O I
10.1038/sj.onc.1201620
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Maintenance of telomere structure by the ribonucleoprotein enzyme telomerase is considered central to the development of most human cancers, However, regulatory mechanisms governing telomerase expression during oncogenesis are largely unknown. We address potential tumour-specific regulation of telomerase RNA gene expression by RNA in situ hybridization to over 300 tumour samples of germ cell and epithelial origin, Twenty-six per cent of non-small cell lung cancers (NSCLC), expressed detectable levels of the telomerase RNA gene (hTR), and interestingly expression was almost confined to squamous carcinomas (41%), being rare in pulmonary adenocarcinomas and large-cell anaplastic carcinomas (P=0.006), Low frequency hTR expression was also associated with adenocarcinoma of the breast (13%), and ovary (17%), In comparison, hTR expression was detected in 43% of cervical cancers with no significant differences in frequency between squamous-cell carcinoma and adenocarcinoma or in transitions between intraepithelial neoplasia and invasive carcinoma, In contrast to the common epithelial cancers, the malignant cells in 73% of testicular germ-cell tumours (seminomas and teratomas), expressed hTR consistent with hTR expression in normal testicular germ cells, Differentiated tissues within ovarian germ cell tumours and in testicular teratomas lacked detectable hTR expression, These studies show that different tumour types have distinct patterns of hTR expression, which has implications for our understanding of mechanisms regulating telomerase activity and for targeting the telomerase RNA component as an anti-cancer therapy.
引用
收藏
页码:979 / 983
页数:5
相关论文
共 21 条
[1]  
BENDA JA, 1994, SEMIN ONCOL, V21, P3
[2]   Telomerase and early detection of cancer: A National Cancer Institute workshop [J].
Breslow, RA ;
Shay, JW ;
Gazdar, AF ;
Srivastava, S .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (09) :618-623
[3]   Telomerase activity in normal and malignant mammalian tissues: Feasibility of telomerase as a target for cancer chemotherapy [J].
Burger, AM ;
Bibby, MC ;
Double, JA .
BRITISH JOURNAL OF CANCER, 1997, 75 (04) :516-522
[4]   THE RNA COMPONENT OF HUMAN TELOMERASE [J].
FENG, JL ;
FUNK, WD ;
WANG, SS ;
WEINRICH, SL ;
AVILION, AA ;
CHIU, CP ;
ADAMS, RR ;
CHANG, E ;
ALLSOPP, RC ;
YU, JH ;
LE, SY ;
WEST, MD ;
HARLEY, CB ;
ANDREWS, WH ;
GREIDER, CW ;
VILLEPONTEAU, B .
SCIENCE, 1995, 269 (5228) :1236-1241
[5]   TELOMERES AND TELOMERASE IN AGING AND CANCER [J].
HARLEY, CB ;
VILLEPONTEAU, B .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1995, 5 (02) :249-255
[6]   Telomerase activity in human breast tumors [J].
Hiyama, E ;
Gollahon, L ;
Kataoka, T ;
Kuroi, K ;
Yokoyama, T ;
Gazdar, AF ;
Hiyama, K ;
Piatyszek, MA ;
Shay, JW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (02) :116-122
[7]   CORRELATING TELOMERASE ACTIVITY LEVELS WITH HUMAN NEUROBLASTOMA OUTCOMES [J].
HIYAMA, E ;
HIYAMA, K ;
YOKOYAMA, T ;
MATSUURA, Y ;
PIATYSZEK, MA ;
SHAY, JW .
NATURE MEDICINE, 1995, 1 (03) :249-255
[8]   TELOMERASE ACTIVITY IN SMALL-CELL AND NON-SMALL-CELL LUNG CANCERS [J].
HIYAMA, K ;
HIYAMA, E ;
ISHIOKA, S ;
YAMAKIDO, M ;
INAI, K ;
GAZDAR, AF ;
PIATYSZEK, MA ;
SHAY, JW .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (12) :895-902
[9]   Refining the telomere-telomerase hypothesis of aging and cancer [J].
Holt, SE ;
Shay, JW ;
Wright, WE .
NATURE BIOTECHNOLOGY, 1996, 14 (07) :836-839
[10]  
Holt SE, 1996, MOL CELL BIOL, V16, P2932