Making alternative splicing decisions during epithelial-to-mesenchymal transition (EMT)

被引:66
作者
Biamonti, Giuseppe [1 ]
Bonomi, Serena [1 ]
Gallo, Stefania [1 ]
Ghigna, Claudia [1 ]
机构
[1] CNR, Ist Genet Mol, I-27100 Pavia, Italy
关键词
Alternative splicing; EMT; Splicing factors; Metastasis; RNA-binding proteins; Tumor progression; RECEPTOR TYROSINE KINASE; MESSENGER-RNA DECAY; TUMORIGENIC ACTIVITIES; CANCER; CD44; RON; GENE; EXON; GROWTH; RAC1B;
D O I
10.1007/s00018-012-0931-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Alternative splicing generates multiple mRNAs from a single transcript and is a major contributor to proteomic diversity and to the control of gene expression in complex organisms. Not surprisingly, this post-transcriptional event is tightly regulated in different tissues and developmental stages. An increasing body of evidences supports a causative role of aberrant alternative splicing in cancer. However, very little is known about its impact on cellular processes crucially involved in tumor progression. The aim of this review is to discuss the link between alternative splicing and the epithelial-to-mesenchymal transition (EMT), one of the major routes by which cancer cells acquire invasive capabilities and become metastatic. We begin with a brief overview of alternative splicing. Next, we discuss alternative splicing factors that regulate EMT. Finally, we provide examples of target genes presenting alternative splicing changes that contribute to the morphological conversions in the EMT process.
引用
收藏
页码:2515 / 2526
页数:12
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