Lack of telomerase activity in lung carcinoids is dependent on human telomerase reverse transcriptase transcription and alternative splicing and is associated with long telomeres

被引:28
作者
Zaffaroni, N
Villa, R
Pastorino, U
Cirincione, R
Incarbone, M
Alloisio, M
Cum, M
Pilotti, S
Daidone, MG
机构
[1] Ist Nazl Studio & Cura Tumori, Dept Expt Oncol, I-20133 Milan, Italy
[2] Ist Nazl Studio & Cura Tumori, Dept Surg, I-20133 Milan, Italy
[3] Ist Nazl Studio & Cura Tumori, Dept Pathol, I-20133 Milan, Italy
[4] Ist Clin Humanitas, Dept Thorac Surg, Milan, Italy
关键词
D O I
10.1158/1078-0432.CCR-04-1293
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Preliminary evidence indicates that telomerase activity is significantly less expressed in typical carcinoids than in large cell neuroendocrine carcinomas or in small cell lung cancers. Knowledge of the mechanisms by which telomerase is differentially regulated in neuroendocrine lung tumors is important for a better understanding of the pathogenesis of these malignancies. Experimental Design: We investigated telomerase activity in 86 neuroendocrine lung tumors and correlated the enzyme activity with the expression of the enzyme subunits [human RNA component (hTR), human telomerase reverse transcriptase (hTERT), and alternatively spliced hTERT variants], with the telomere-associated protein human protection of telomere-1, and with the telomere length pattern. Results: A significantly (P = 0.0001) lower frequency of telomerase-positive cases was found in typical carcinoids (14%) than in large cell neuroendocrine carcinomas (87%) and small cell lung cancers (92%). hTR was constitutively expressed in all carcinoids. Telomerase-negative carcinoids were characterized by the absence of any hTERT transcript, only displayed the beta(-) alternatively spliced variant, or concomitantly expressed the alpha(+)beta(+) full-length message with different combinations of alternatively spliced variants. However, in these tumors, a more abundant level of alternatively spliced transcripts than that of the alpha(+)beta(+) full-length transcript was generally found. No significant difference was observed in human protection of telomere-1 expression between telomerase-negative and telomerase-positive carcinoids. Telomeres were significantly (P < 0.05) longer in telomerase-negative carcinoids than in telomerase-positive carcinoids (median value, 9.15 versus 4.47 kb). However, alternative lengthening of telomeres, as shown by associated promyelocytic leukemia bodies, was not observed in these tumors. Conclusions: Our results indicate that telomerase is repressed in most lung carcinoids and that hTERT transcription and alternative splicing play a role in such a negative regulation. Moreover, the absence of any telomerase maintenance mechanism may contribute to the favorable prognosis of this malignancy.
引用
收藏
页码:2832 / 2839
页数:8
相关论文
共 58 条
[11]   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
[12]   The hTERTα splice variant is a dominant negative inhibitor of telomerase activity [J].
Colgin, LM ;
Wilkinson, C ;
Englezou, A ;
Kilian, A ;
Robinson, MO ;
Reddel, RR .
NEOPLASIA, 2000, 2 (05) :426-432
[13]   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
[14]   Telomerase activity in pulmonary neuroendocrine tumors -: Correlation with histologic subtype (MS-0060) [J].
Gómez-Román, JJ ;
Romero, AF ;
Castro, LS ;
Nieto, EH ;
Fernández-Luna, JL ;
Val-Bernal, JF .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2000, 24 (03) :417-421
[15]  
GOULD VE, 1983, LAB INVEST, V49, P519
[16]   Creation of human tumour cells with defined genetic elements [J].
Hahn, WC ;
Counter, CM ;
Lundberg, AS ;
Beijersbergen, RL ;
Brooks, MW ;
Weinberg, RA .
NATURE, 1999, 400 (6743) :464-468
[17]   Human telomerase contains evolutionarily conserved catalytic and structural subunits [J].
Harrington, L ;
Zhou, W ;
McPhail, T ;
Oulton, R ;
Yeung, DSK ;
Mar, V ;
Bass, MB ;
Robinson, MO .
GENES & DEVELOPMENT, 1997, 11 (23) :3109-3115
[18]   Alternative lengthening of telomeres in mammalian cells [J].
Henson, JD ;
Neumann, AA ;
Yeager, TR ;
Reddel, RR .
ONCOGENE, 2002, 21 (04) :598-610
[19]   Functional requirement of p23 and Hsp90 in telomerase complexes [J].
Holt, SE ;
Aisner, DL ;
Baur, J ;
Tesmer, VM ;
Dy, M ;
Ouellette, M ;
Trager, JB ;
Morin, GB ;
Toft, DO ;
Shay, JW ;
Wright, WE ;
White, MA .
GENES & DEVELOPMENT, 1999, 13 (07) :817-826
[20]   Two prognostically significant subtypes of high-grade lung neuroendocrine turnours independent of small-cell and large-cell neuroendocrine carcinomas identified by gene expression profiles [J].
Jones, MH ;
Virtanen, C ;
Honjoh, D ;
Miyoshi, T ;
Satoh, Y ;
Okumura, S ;
Nakagawa, K ;
Nomura, H ;
Ishikawa, Y .
LANCET, 2004, 363 (9411) :775-781