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Multidimensional regulatory roles and therapeutic applications of SRSF7 in cancer
Yuan Li1, Huimeng Gao1, Xuanyu Zhang1
1Department of Oral Biology, School and Hospital of Stomatology, China Medical University, Liaoning Province Key Laboratory of Oral Disease, Shenyang, Liaoning, 110002, China.
Abstract:
Malignant tumors, as one of the leading causes of mortality, pose great threats to global public health. Serine/Arginine-rich Splicing Factor 7 (SRSF7), a core splicing regulatory protein of the SRSF family, plays a crucial role in maintaining RNA stability, facilitating alternative splicing, and assisting RNA nuclear export. It also exhibits significantly aberrant expression among various cancers, including lung, colorectal, liver, and oral cancer. This review examines the molecular mechanisms of SRSF7 in tumorigenesis, with a focus on its role in the epigenetic reprogramming of related tumors. Specifically, it explores the abnormal regulation of the cell cycle, the regulation of non-coding RNA, the control of RNA methylation, and the reprogramming of glucose metabolism. Additionally, this review examines the role of SRSF7 in the tumor immune microenvironment through alternative splicing and immune evasion through the immune checkpoint PD-1. It also highlights the role of SRSF family members in tumor resistance, illustrating how alternative splicing contributes to tumor chemoresistance. Although SRSF7 shows significant promise in tumor intervention therapies, more experimental and clinical studies are still needed to evaluate its clinical application. This review enhances our understanding of the molecular landscape of SRSF7 in tumorigenesis with great potential to become a key node in tumor-targeted therapy and companion diagnostics, driving translational potential from mechanisms to clinical applications.
Insights
Serine/Arginine-rich Splicing Factor 7 (SRSF7) is crucial in cancer development and progression. Understanding SRSF7
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- Malignant tumors are a leading cause of mortality worldwide.
- Serine/Arginine-rich Splicing Factor 7 (SRSF7) is a key splicing regulator implicated in various cancers.
- Aberrant SRSF7 expression is observed in lung, colorectal, liver, and oral cancers.
Purpose of the Study:
- To review the molecular mechanisms of SRSF7 in tumorigenesis.
- To focus on SRSF7's role in epigenetic reprogramming within tumors.
- To explore SRSF7's involvement in cancer progression, immune evasion, and therapeutic resistance.
Main Methods:
- Literature review of studies on SRSF7 function in cancer.
- Analysis of SRSF7's role in cell cycle regulation, non-coding RNA, RNA methylation, and glucose metabolism.
- Examination of SRSF7's impact on the tumor immune microenvironment and immune checkpoint PD-1.
Main Results:
- SRSF7 influences epigenetic reprogramming, cell cycle control, non-coding RNA, RNA methylation, and glucose metabolism in tumors.
- SRSF7 contributes to immune evasion via alternative splicing and PD-1 immune checkpoint.
- SRSF7 family members play a role in tumor resistance, including chemoresistance, through alternative splicing.
Conclusions:
- SRSF7 is a significant factor in tumorigenesis and cancer progression.
- SRSF7 presents potential as a target for tumor intervention therapies and companion diagnostics.
- Further experimental and clinical studies are necessary to validate SRSF7's clinical applications.
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