Alternative Splicing: Expanding the Landscape of Cancer Biomarkers and Therapeutics

International Journal of Molecular Sciences

Paulo Matos¹  Cláudia Bessa¹  Vânia Gonçalves¹  Peter Jordan¹ 

[1] Department of Human Genetics, National Health Institute Dr. Ricardo Jorge, 1649-016 Lisbon, Portugal;

关键词: pre-messenger RNA;    alternative splicing;    mutation;    cancer progression;    splicing factor;    signal transduction;   

DOI  :  10.3390/ijms21239032

来源: DOAJ

【 摘 要 】

Alternative splicing (AS) is a critical post-transcriptional regulatory mechanism used by more than 95% of transcribed human genes and responsible for structural transcript variation and proteome diversity. In the past decade, genome-wide transcriptome sequencing has revealed that AS is tightly regulated in a tissue- and developmental stage-specific manner, and also frequently dysregulated in multiple human cancer types. It is currently recognized that splicing defects, including genetic alterations in the spliced gene, altered expression of both core components or regulators of the precursor messenger RNA (pre-mRNA) splicing machinery, or both, are major drivers of tumorigenesis. Hence, in this review we provide an overview of our current understanding of splicing alterations in cancer, and emphasize the need to further explore the cancer-specific splicing programs in order to obtain new insights in oncology. Furthermore, we also discuss the recent advances in the identification of dysregulated splicing signatures on a genome-wide scale and their potential use as biomarkers. Finally, we highlight the therapeutic opportunities arising from dysregulated splicing and summarize the current approaches to therapeutically target AS in cancer.

【 授权许可】

Unknown