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J Nucleic Acids. 2012;2012:269570. doi: 10.1155/2012/269570. Epub 2011 Oct 24.

Splicing programs and cancer.

Journal of nucleic acids

Sophie Germann, Lise Gratadou, Martin Dutertre, Didier Auboeuf

Affiliations

  1. Université de Lyon, 28 rue Laënnec, 69008 Lyon, France.

PMID: 22132318 PMCID: PMC3202119 DOI: 10.1155/2012/269570

Abstract

Numerous studies report splicing alterations in a multitude of cancers by using gene-by-gene analysis. However, understanding of the role of alternative splicing in cancer is now reaching a new level, thanks to the use of novel technologies allowing the analysis of splicing at a large-scale level. Genome-wide analyses of alternative splicing indicate that splicing alterations can affect the products of gene networks involved in key cellular programs. In addition, many splicing variants identified as being misregulated in cancer are expressed in normal tissues. These observations suggest that splicing programs contribute to specific cellular programs that are altered during cancer initiation and progression. Supporting this model, recent studies have identified splicing factors controlling cancer-associated splicing programs. The characterization of splicing programs and their regulation by splicing factors will allow a better understanding of the genetic mechanisms involved in cancer initiation and progression and the development of new therapeutic targets.

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