Deregulation of splicing factors and breast cancer development.

Abstract

It is well known that many genes implicated in the development and progression of breast cancer undergo aberrant alternative splicing events to produce proteins with pro-cancer properties. These changes in alternative splicing can arise from mutations or single-nucleotide polymorphisms (SNPs) within the DNA sequences of cancer-related genes, which can strongly affect the activity of splicing factors and influence the splice site choice. However, it is important to note that absence of mutations is not sufficient to prevent misleading choices in splice site selection. There is now increasing evidence to demonstrate that the expression profile of ten splicing factors (including SRs and hnRNPs) and eight RNA-binding proteins changes in breast cancer cells compared with normal cells. These modifications strongly influence the alternative splicing pattern of many cancer-related genes despite the absence of any detrimental mutations within their DNA sequences. Thus, a comprehensive assessment of the splicing factor status in breast cancer is important to provide insights into the mechanisms that lead to breast cancer development and metastasis. Whilst most studies focus on mutations that affect alternative splicing in cancer-related genes, this review focuses on splicing factors and RNA-binding proteins that are themselves deregulated in breast cancer and implicated in cancer-related alternative splicing events.

• Authors: Marco Silipo, Hannah Gautrey, Alison Tyson-Capper
• Journal: Journal of molecular cell biology (J Mol Cell Biol) Vol. 7 Issue 5 Pg. 388-401 (Oct 2015) ISSN: 1759-4685 [Electronic] United States
• PMID: 25948865 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
• Copyright: © The Author (2015). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. All rights reserved.

Chemical References

• RNA-Binding Proteins

Topics

• Alternative Splicing (genetics, physiology)
• Animals
• Breast Neoplasms (genetics, metabolism)
• Female
• Gene Expression Regulation, Neoplastic (genetics, physiology)
• Humans
• RNA Splicing (genetics)
• RNA-Binding Proteins (genetics, metabolism)