GAS5, a non-protein-coding RNA, controls apoptosis and is downregulated in breast cancer

被引:678
作者
Mourtada-Maarabouni, M. [1 ,2 ]
Pickard, M. R. [1 ,2 ]
Hedge, V. L. [1 ,2 ]
Farzaneh, F. [3 ]
Williams, G. T. [1 ,2 ]
机构
[1] Univ Keele, Inst Sci & Technol Med, Keele ST5 5BG, Staffs, England
[2] Univ Keele, Sch Life Sci, Keele ST5 5BG, Staffs, England
[3] Kings Coll London, Dept Haematol Med, Rayne Inst, London WC2R 2LS, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
apoptosis; snoRNA; growth arrest; oncogenesis; breast cancer; drug resistance; EXPRESSION CLONING REVEALS; HUMAN PROSTATIC-CARCINOMA; SMALL NUCLEOLAR RNAS; SNORNA HOST GENE; B-CELL LYMPHOMA; GROWTH-ARREST; FUNCTIONAL EXPRESSION; MOLECULAR REGULATION; NONCODING RNAS; IN-VITRO;
D O I
10.1038/onc.2008.373
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
Effective control of both cell survival and cell proliferation is critical to the prevention of oncogenesis and to successful cancer therapy. Using functional expression cloning, we have identified GAS5 ( growth arrest-specific transcript 5) as critical to the control of mammalian apoptosis and cell population growth. GAS5 transcripts are subject to complex post-transcriptional processing and some, but not all, GAS5 transcripts sensitize mammalian cells to apoptosis inducers. We have found that, in some cell lines, GAS5 expression induces growth arrest and apoptosis independently of other stimuli. GAS5 transcript levels were significantly reduced in breast cancer samples relative to adjacent unaffected normal breast epithelial tissues. The GAS5 gene has no significant protein-coding potential but expression encodes small nucleolar RNAs (snoRNAs) in its introns. Taken together with the recent demonstration of tumor suppressor characteristics in the related snoRNA U50, our observations suggest that such snoRNAs form a novel family of genes controlling oncogenesis and sensitivity to therapy in cancer.
引用
收藏
页码:195 / 208
页数:14
相关论文
共 64 条
[1]  
BERTHON P, 1995, INT J ONCOL, V6, P333
[2]   The death-associated protein kinases: Structure, function, and beyond [J].
Bialik, Shani ;
Kimchi, Adi .
ANNUAL REVIEW OF BIOCHEMISTRY, 2006, 75 :189-210
[3]   Combined effect of tumor necrosis factor-related apoptosis-inducing ligand and ionizing radiation in breast cancer therapy [J].
Chinnaiyan, AM ;
Prasad, U ;
Shankar, S ;
Hamstra, DA ;
Shanaiah, M ;
Chenevert, TL ;
Ross, BD ;
Rehemtulla, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (04) :1754-1759
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]   REGULATION AND EXPRESSION OF A GROWTH ARREST-SPECIFIC GENE (GAS5) DURING GROWTH, DIFFERENTIATION, AND DEVELOPMENT [J].
COCCIA, EM ;
CICALA, C ;
CHARLESWORTH, A ;
CICCARELLI, C ;
ROSSI, GB ;
PHILIPSON, L ;
SORRENTINO, V .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (08) :3514-3521
[6]   IMMUNOLOGICAL SELECTION OF VARIANT MOUSE LYMPHOID-CELLS WITH ALTERED GLUCOCORTICOID RESPONSIVENESS [J].
DANIELSEN, M ;
PETERSON, DO ;
STALLCUP, MR .
MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (07) :1310-1316
[7]   IDENTIFICATION OF A NOVEL SERINE THREONINE KINASE AND A NOVEL 15-KD PROTEIN AS POTENTIAL MEDIATORS OF THE GAMMA-INTERFERON-INDUCED CELL-DEATH [J].
DEISS, LP ;
FEINSTEIN, E ;
BERISSI, H ;
COHEN, O ;
KIMCHI, A .
GENES & DEVELOPMENT, 1995, 9 (01) :15-30
[8]   SnoRNA U50 is a candidate tumor-suppressor gene at 6q14.3 with a mutation associated with clinically significant prostate cancer [J].
Dong, Xue-Yuan ;
Rodriguez, Carmen ;
Guo, Peng ;
Sun, Xiaodong ;
Talbot, Jeffrey T. ;
Zhou, Wei ;
Petros, John ;
Li, Qunna ;
Vessella, Robert L. ;
Kibel, Adam S. ;
Stevens, Victoria L. ;
Calle, Eugenia E. ;
Dong, Jin-Tang .
HUMAN MOLECULAR GENETICS, 2008, 17 (07) :1031-1042
[9]  
FAN SJ, 1995, CANCER RES, V55, P1649
[10]  
Fleming JV, 1998, BIOCHEM J, V330, P573