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Updated: Aug 17, 2025

Detection of Alternative Splicing During Epithelial-Mesenchymal Transition
Published on: October 9, 2014
Emerging roles of alternative RNA splicing in oral squamous cell carcinoma
Miaomiao Liu1, Jihua Guo1,2, Rong Jia1,3
1The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST) & Key Laboratory of Oral Biomedicine Ministry of Education, School & Hospital of Stomatology, Wuhan University, Wuhan, China.
Abstract:
Alternative RNA splicing (ARS) is an essential and tightly regulated cellular process of post-transcriptional regulation of pre-mRNA. It produces multiple isoforms and may encode proteins with different or even opposite functions. The dysregulated ARS of pre-mRNA contributes to the development of many cancer types, including oral squamous cell carcinoma (OSCC), and may serve as a biomarker for the diagnosis and prognosis of OSCC and an attractive therapeutic target. ARS is mainly regulated by splicing factors, whose expression is also often dysregulated in OSCC and involved in tumorigenesis. This review focuses on the expression and roles of splicing factors in OSCC, the alternative RNA splicing events associated with OSCC, and recent advances in therapeutic approaches that target ARS.
Insights
Alternative RNA splicing (ARS) alterations drive oral cancer. Dysregulated splicing factors and ARS events in oral squamous cell carcinoma (OSCC) offer diagnostic biomarkers and therapeutic targets.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- Alternative RNA splicing (ARS) is a crucial post-transcriptional regulatory mechanism.
- ARS generates diverse protein isoforms from a single gene, impacting cellular functions.
- Dysregulation of ARS is implicated in various cancers, including oral squamous cell carcinoma (OSCC).
Purpose of the Study:
- To review the expression and roles of splicing factors in OSCC.
- To examine alternative RNA splicing events associated with OSCC development.
- To discuss recent therapeutic strategies targeting ARS in OSCC.
Main Methods:
- Literature review of studies on ARS, splicing factors, and OSCC.
- Analysis of the impact of splicing factor dysregulation on OSCC tumorigenesis.
- Synthesis of current knowledge on ARS-related biomarkers and therapeutic targets in OSCC.
Main Results:
- Splicing factors are frequently dysregulated in OSCC and contribute to cancer progression.
- Specific ARS events are characteristic of OSCC and can serve as diagnostic/prognostic indicators.
- Targeting ARS pathways presents a promising therapeutic avenue for OSCC.
Conclusions:
- ARS dysregulation and altered splicing factor expression are key events in OSCC.
- ARS-based biomarkers hold potential for OSCC diagnosis and prognosis.
- Targeting ARS offers a novel therapeutic strategy for oral cancer treatment.
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