The RNA-binding protein Sam68 is a multifunctional player in human cancer

被引:125
作者
Bielli, Pamela [1 ,2 ]
Busa, Roberta [1 ,2 ]
Paola Paronetto, Maria [3 ]
Sette, Claudio [1 ,2 ]
机构
[1] Univ Roma Tor Vergata, Dept Publ Hlth & Cell Biol, I-00133 Rome, Italy
[2] IRCSS Fdn Santa Lucia, Lab Neuroembryol, I-00143 Rome, Italy
[3] Ctr Regulacio Genom, Barcelona 08003, Spain
关键词
SPLICING REGULATOR SAM68; BLOOD MONONUCLEAR-CELLS; FAMILY TYROSINE KINASES; SRC HOMOLOGY 3; MESSENGER-RNA; FUNCTIONAL INTERACTION; SIGNAL-TRANSDUCTION; ADAPTER PROTEIN; BREAST-CANCER; C-SRC;
D O I
10.1530/ERC-11-0041
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Src associated in mitosis, of 68 kDa (Sam68) is a KH domain RNA-binding protein that belongs to the signal transduction and activation of RNA family. Although ubiquitously expressed, Sam68 plays very specialized roles in different cellular environments. In most cells, Sam68 resides in the nucleus and is involved in several steps of mRNA processing, from transcription, to alternative splicing, to nuclear export. In addition, Sam68 translocates to the cytoplasm upon cell stimulation, cell cycle transitions or viral infections, where it takes part to signaling complexes and associates with the mRNA translation machinery. Recent evidence has linked Sam68 function to the onset and progression of endocrine tumors, such as prostate and breast carcinomas. Notably, all the biochemical activities reported for Sam68 seem to be implicated in carcinogenesis. Herein, we review the recent advancement in the knowledge of Sam68 function and regulation and discuss it in the frame of its participation to neoplastic transformation and tumor progression. Endocrine-Related Cancer (2011) 18 R91-R102
引用
收藏
页码:R91 / R102
页数:12
相关论文
共 93 条
[1]   Regulatory intramolecular association in a tyrosine kinase of the Tec family [J].
Andreotti, AH ;
Bunnell, SC ;
Feng, S ;
Berg, LJ ;
Schreiber, SL .
NATURE, 1997, 385 (6611) :93-97
[2]   SUMO modification of Sam68 enhances its ability to repress cyclin D1 expression and inhibits its ability to induce apoptosis [J].
Babic, I. ;
Cherry, E. ;
Fujita, D. J. .
ONCOGENE, 2006, 25 (36) :4955-4964
[3]   The RNA binding protein Sam68 is acetylated in tumor cell lines, and its acetylation correlates with enhanced RNA binding activity [J].
Babic, I ;
Jakymiw, A ;
Fujita, DJ .
ONCOGENE, 2004, 23 (21) :3781-3789
[4]   BRK tyrosine kinase expression in a high proportion of human breast carcinomas [J].
Barker, KT ;
Jackson, LE ;
Crompton, MR .
ONCOGENE, 1997, 15 (07) :799-805
[5]   The human SWI/SNF subunit Brm is a regulator of alternative splicing [J].
Batsché, E ;
Yaniv, M ;
Muchardt, C .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2006, 13 (01) :22-29
[6]   Arginine methylation inhibits the binding of proline-rich ligands to Src homology 3, but not WW, domains [J].
Bedford, MT ;
Frankel, A ;
Yaffe, MB ;
Clarke, S ;
Leder, P ;
Richard, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (21) :16030-16036
[7]   Ablation of the Sam68 gene impairs female fertility and gonadotropin-dependent follicle development [J].
Bianchi, Enrica ;
Barbagallo, Federica ;
Valeri, Claudia ;
Geremia, Raffaele ;
Salustri, Antonietta ;
De Felici, Massimo ;
Sette, Claudio .
HUMAN MOLECULAR GENETICS, 2010, 19 (24) :4886-4894
[8]   Tyrosine kinase signalling in breast cancer - Epidermal growth factor receptor and c-Src interactions in breast cancer [J].
Biscardi, JS ;
Ishizawar, RC ;
Silva, CM ;
Parsons, SJ .
BREAST CANCER RESEARCH, 2000, 2 (03) :203-210
[9]   Mechanisms of alternative pre-messenger RNA splicing [J].
Black, DL .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :291-336
[10]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608