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
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共 43 条
[11]  
Collesi C, 1996, MOL CELL BIOL, V16, P5518
[12]   A functional role for KLF6-SV1 in lung adenocarcinoma prognosis and chemotherapy response [J].
Difeo, Analisa ;
Feld, Lauren ;
Rodriguez, Estefania ;
Wang, Christine ;
Beer, David G. ;
Martignetti, John A. ;
Narla, Goutham .
CANCER RESEARCH, 2008, 68 (04) :965-970
[13]   Identification of BRCA1-IRIS, a BRCA1 locus product [J].
ElShamy, WM ;
Livingston, DM .
NATURE CELL BIOLOGY, 2004, 6 (10) :954-+
[14]   MicroRNA-29 family reverts aberrant methylation in lung cancer by targeting DNA methyltransferases 3A and 3B [J].
Fabbri, Muller ;
Garzon, Ramiro ;
Cimmino, Amelia ;
Liu, Zhongfa ;
Zanesi, Nicola ;
Callegari, Elisa ;
Liu, Shujun ;
Alder, Hansjuerg ;
Costinean, Stefan ;
Fernandez-Cymering, Cecilia ;
Volinia, Stefano ;
Guler, Gulnur ;
Morrison, Carl D. ;
Chan, Kenneth K. ;
Marcucci, Guido ;
Calin, George A. ;
Huebner, Kay ;
Croce, Carlo M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (40) :15805-15810
[15]  
Furuta K, 1998, CLIN CANCER RES, V4, P21
[16]   Cell motility is controlled by SF2/ASF through alternative splicing of the Ron protooncogene [J].
Ghigna, C ;
Giordano, S ;
Shen, HH ;
Benvenuto, F ;
Castiglioni, F ;
Comoglio, PM ;
Green, MR ;
Riva, S ;
Biamonti, G .
MOLECULAR CELL, 2005, 20 (06) :881-890
[17]   Identification of alternatively spliced mRNA variants related to cancers by genome-wide ESTs alignment [J].
Hui, LJ ;
Zhang, X ;
Wu, X ;
Lin, ZX ;
Wang, QK ;
Li, YX ;
Hu, GX .
ONCOGENE, 2004, 23 (17) :3013-3023
[18]   Insights into the connection between cancer and alternative splicing [J].
Kim, Eddo ;
Goren, Amir ;
Ast, Gil .
TRENDS IN GENETICS, 2008, 24 (01) :7-10
[19]   Multiple alternative splicing markers for ovarian cancer [J].
Klinck, Roscoe ;
Bramard, Anne ;
Inkel, Lyna ;
Dufresne-Martin, Genevieve ;
Gervais-Bird, Julien ;
Madden, Richard ;
Paquet, Eric R. ;
Koh, ChuShin ;
Venables, Julian P. ;
Prinos, Panagiotis ;
Jilaveanu-Pelmus, Manuela ;
Wellinger, Raymund ;
Rancourt, Claudine ;
Chabot, Benoit ;
Abou Elela, Sherif .
CANCER RESEARCH, 2008, 68 (03) :657-663
[20]   Alterations in Gemin5 expression contribute to alternative mRNA splicing patterns and tumor cell motility [J].
Lee, Jong Heun ;
Horak, Christine E. ;
Khanna, Chand ;
Meng, Zhaojing ;
Yu, Li Rong ;
Veenstra, Timothy D. ;
Steeg, Patricia S. .
CANCER RESEARCH, 2008, 68 (03) :639-644