She Wenting, Shao Jun, Jia Rong
The 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.
Department of Stomatology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, China.
Front Cell Dev Biol. 2021 Nov 30;9:780023. doi: 10.3389/fcell.2021.780023. eCollection 2021.
Aberrant alternative splicing of pre-mRNA is an emerging cancer hallmark. Many cancer-associated genes undergo alternative splicing to produce multiple isoforms with diverse or even antagonistic functions. Oncogenic isoforms are often up-regulated, whereas tumor suppressive isoforms are down-regulated during tumorigenesis. Serine/arginine-rich splicing factor 6 (SRSF6) is an important splicing factor that regulates the alternative splicing of hundreds of target genes, including many cancer-associated genes. The potential roles of SRSF6 in cancers have attracted increasing attentions in the past decade. Accumulated pieces of evidence have shown that SRSF6 is a potential oncogenic gene that promotes oncogenic splicing when overexpressed. Targeting SRSF6 may suppress tumorigenesis. In this review, we describe the gene, mRNA, and protein structure of SRSF6; summarize the current understanding of the expression, functions, and regulatory mechanisms of SRSF6 during tumorigenesis; and discuss the potential application of targeting SRSF6 in cancer treatment.
前体mRNA的异常可变剪接是一种新出现的癌症标志。许多与癌症相关的基因会发生可变剪接,以产生具有不同甚至拮抗功能的多种异构体。在肿瘤发生过程中,致癌异构体往往上调,而肿瘤抑制异构体则下调。富含丝氨酸/精氨酸的剪接因子6(SRSF6)是一种重要的剪接因子,可调节数百个靶基因的可变剪接,其中包括许多与癌症相关的基因。在过去十年中,SRSF6在癌症中的潜在作用已引起越来越多的关注。越来越多的证据表明,SRSF6是一种潜在的致癌基因,过表达时会促进致癌剪接。靶向SRSF6可能会抑制肿瘤发生。在这篇综述中,我们描述了SRSF6的基因、mRNA和蛋白质结构;总结了目前对SRSF6在肿瘤发生过程中的表达、功能和调控机制的理解;并讨论了靶向SRSF6在癌症治疗中的潜在应用。