School of Life Science and Technology, Harbin Institute of Technology, Harbin, China.
Key Laboratory of Biological Big Data (Harbin Institute of Technology), Ministry of Education, Harbin, China.
Oncogene. 2021 Sep;40(35):5441-5450. doi: 10.1038/s41388-021-01947-7. Epub 2021 Jul 20.
Great progress has been made in the investigation on mutation and expression of splicing factor. However, little is known on the role of alternative splicing of splicing factors across cancers. Here, we reported a pan-cancer analysis of alternative splicing of splicing factors spanning 6904 patients across 16 cancer types, and identified 167 splicing factors with implications regulating cancer-specific splicing patterns through alternative splicing. Furthermore, we found that abnormal splicing events of splicing factors could serve as potential common regulators for alternative splicing in different cancers. In addition, we developed a splicing-derived neoepitopes database (ASPNs), which provided the corresponding putative alternative splicing-derived neoepitopes of 16 cancer types. Our results suggested that alternative splicing of splicing factors involved in the pre-RNA splicing process was common across cancer types and may represent an underestimated hallmark of tumorigenesis.
在剪接因子的突变和表达研究方面已经取得了很大的进展。然而,对于剪接因子在各种癌症中的可变剪接作用知之甚少。在这里,我们报告了一项跨越 16 种癌症类型的 6904 名患者的剪接因子可变剪接的泛癌症分析,并确定了 167 个剪接因子,它们通过可变剪接影响调节癌症特异性剪接模式。此外,我们发现剪接因子的异常剪接事件可以作为不同癌症中可变剪接的潜在共同调节剂。此外,我们开发了一个剪接衍生新表位数据库(ASPNs),该数据库提供了 16 种癌症相应的假定的剪接衍生新表位。我们的结果表明,参与 pre-RNA 剪接过程的剪接因子的可变剪接在癌症类型中是常见的,这可能代表了肿瘤发生的一个被低估的特征。