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SRSF3作为癌症治疗靶点的新作用

Emerging Roles of SRSF3 as a Therapeutic Target for Cancer.

作者信息

Zhou Zhixia, Gong Qi, Lin Zhijuan, Wang Yin, Li Mengkun, Wang Lu, Ding Hongfei, Li Peifeng

机构信息

Institute for Translational Medicine, The Affiliated Hospital of Qingdao University, College of Medicine, Qingdao University, Qingdao, China.

Departments of Pediatrics, Second Clinical Medical College of Qingdao University, Qingdao, China.

出版信息

Front Oncol. 2020 Sep 25;10:577636. doi: 10.3389/fonc.2020.577636. eCollection 2020.

Abstract

Ser/Arg-rich (SR) proteins are RNA-binding proteins known as constitutive and alternative splicing (AS) regulators that regulate multiple aspects of the gene expression program. Ser/Arg-rich splicing factor 3 (SRSF3) is the smallest member of the SR protein family, and its level is controlled by multiple factors and involves complex mechanisms in eukaryote cells, whereas the aberrant expression of SRSF3 is associated with many human diseases, including cancer. Here, we review state-of-the-art research on SRSF3 in terms of its function, expression, and misregulation in human cancers. We emphasize the negative consequences of the overexpression of the SRSF3 oncogene in cancers, the pathways underlying SRSF3-mediated transformation, and implications of potential anticancer drugs by downregulation of SRSF3 expression for cancer therapy. Cumulative research on SRSF3 provides critical insight into its essential part in maintaining cellular processes, offering potential new targets for anti-cancer therapy.

摘要

富含丝氨酸/精氨酸(SR)的蛋白质是一类RNA结合蛋白,作为组成型和可变剪接(AS)调节因子,调控基因表达程序的多个方面。富含丝氨酸/精氨酸剪接因子3(SRSF3)是SR蛋白家族中最小的成员,其水平受多种因素控制,在真核细胞中涉及复杂机制,而SRSF3的异常表达与包括癌症在内的多种人类疾病相关。在此,我们综述了关于SRSF3在人类癌症中的功能、表达和调控异常的最新研究。我们强调了SRSF3癌基因在癌症中过表达的负面后果、SRSF3介导的转化所涉及的途径,以及通过下调SRSF3表达实现潜在抗癌药物对癌症治疗的意义。对SRSF3的累积研究为其在维持细胞过程中的重要作用提供了关键见解,为抗癌治疗提供了潜在的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c975/7544984/704fe69f2f78/fonc-10-577636-g0001.jpg

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