Aberrant RNA splicing and its functional consequences in cancer cells

被引:85
作者
Fackenthal, James D. [1 ,2 ]
Godley, Lucy A. [1 ,2 ]
机构
[1] Univ Chicago, Hematol Oncol Sect, Dept Med, Chicago, IL 60637 USA
[2] Univ Chicago, Canc Res Ctr, Chicago, IL 60637 USA
关键词
D O I
10.1242/dmm.000331
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Among the myriad of alterations present in cancer cells are an abundance of aberrant mRNA transcripts. Whether abnormal gene transcription is a by-product of cellular transformation or whether it represents an inherent element that contributes to the properties of cancer cells is not yet clear. Here, we present growing evidence that in many cases, aberrant mRNA transcripts contribute to essential phenotypes associated with transformed cells, suggesting that alterations in the splicing machinery are common and functionally important for cancer development. The proteins encoded by these abnormal transcripts are often truncated or missing domains, thereby altering protein function or conferring new functions altogether. Thus, aberrant splicing regulation has genome-wide effects, potentially altering gene expression in many cancer-associated pathways.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 43 条
[1]  
Adams M, 2002, CANCER RES, V62, P3289
[2]   Changes in WT1 splicing are associated with a specific gene expression profile in Wilms' tumour [J].
Baudry, D ;
Faussillon, M ;
Cabanis, MO ;
Rigolet, M ;
Zucker, JM ;
Patte, C ;
Sarnacki, S ;
Boccon-Gibod, L ;
Junien, C ;
Jeanpierre, C .
ONCOGENE, 2002, 21 (36) :5566-5573
[3]   Mammary epithelial-mesenchymal interaction regulates fibronectin alternative splicing via phosphatidylinositol 3-kinase [J].
Blaustein, M ;
Pelisch, F ;
Coso, OA ;
Bissell, MJ ;
Kornblihtt, AR ;
Srebrow, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (20) :21029-21037
[4]   Signals, pathways and splicing regulation [J].
Blaustein, Matias ;
Pelisch, Federico ;
Srebrow, Anabella .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (11) :2031-2048
[5]   Alternative splicing: New insights from global analyses [J].
Blencowe, Benjamin J. .
CELL, 2006, 126 (01) :37-47
[6]   RNA-based analysis of BRCA1 and BRCA2 gene alterations [J].
Bonatti, Fabrizia ;
Pepe, Chiara ;
Tancredi, Mariella ;
Lombardi, Grazia ;
Aretini, Paolo ;
Sensi, Elisa ;
Falaschi, Elisabetta ;
Cipollini, Giovanna ;
Bevilacqua, Generoso ;
Caligo, Maria Adelaide .
CANCER GENETICS AND CYTOGENETICS, 2006, 170 (02) :93-101
[7]   Alternative spliced transcripts as cancer markers [J].
Caballero, OL ;
de Souza, SJ ;
Brentani, RR ;
Simpson, AJG .
DISEASE MARKERS, 2001, 17 (02) :67-75
[8]   Intronic alterations in BRCA1 and BRCA2:: Effect on mRNA splicing fidelity and expression [J].
Chen, XW ;
Truong, TTN ;
Weaver, J ;
Bove, BA ;
Cattie, K ;
Armstrong, BA ;
Daly, MB ;
Godwin, AK .
HUMAN MUTATION, 2006, 27 (05) :427-435
[9]   Method of predicting Splice Sites based on signal interactions [J].
Churbanov, Alexander ;
Rogozin, Igor B. ;
Deogun, Jitender S. ;
Ali, Hesham .
BIOLOGY DIRECT, 2006, 1 (1)
[10]   Differentiating pathogenic mutations from polymorphic alterations in the splice sites of BRCA1 and BRCA2 [J].
Claes, K ;
Poppe, B ;
Machackova, E ;
Coene, I ;
Foretova, L ;
De Paepe, A ;
Messiaen, L .
GENES CHROMOSOMES & CANCER, 2003, 37 (03) :314-320