Federico Antonio, Rienzo Monica, Abbondanza Ciro, Costa Valerio, Ciccodicola Alfredo, Casamassimi Amelia
Institute of Genetics and Biophysics "Adriano Buzzati Traverso", CNR, 80131 Naples, Italy.
Department of Science and Technology, University of Naples "Parthenope", 80143 Naples, Italy.
Int J Mol Sci. 2017 Apr 29;18(5):936. doi: 10.3390/ijms18050936.
The integrator complex has been recently identified as a key regulator of RNA Polymerase II-mediated transcription, with many functions including the processing of small nuclear RNAs, the pause-release and elongation of polymerase during the transcription of protein coding genes, and the biogenesis of enhancer derived transcripts. Moreover, some of its components also play a role in genome maintenance. Thus, it is reasonable to hypothesize that their functional impairment or altered expression can contribute to malignancies. Indeed, several studies have described the mutations or transcriptional alteration of some Integrator genes in different cancers. Here, to draw a comprehensive pan-cancer picture of the genomic and transcriptomic alterations for the members of the complex, we reanalyzed public data from The Cancer Genome Atlas. Somatic mutations affecting Integrator subunit genes and their transcriptional profiles have been investigated in about 11,000 patients and 31 tumor types. A general heterogeneity in the mutation frequencies was observed, mostly depending on tumor type. Despite the fact that we could not establish them as cancer drivers, and genes were highly mutated in specific cancers. A transcriptome analysis of paired (normal and tumor) samples revealed that the transcription of , , and is significantly altered in several cancers. Experimental validation performed on primary tumors confirmed these findings.
整合子复合体最近被确定为RNA聚合酶II介导转录的关键调节因子,具有多种功能,包括小核RNA的加工、蛋白质编码基因转录过程中聚合酶的暂停释放和延伸,以及增强子衍生转录本的生物合成。此外,其一些组分在基因组维持中也发挥作用。因此,合理推测其功能受损或表达改变可能导致恶性肿瘤。事实上,多项研究已经描述了不同癌症中一些整合子基因的突变或转录改变。在此,为了全面描绘该复合体成员在泛癌中的基因组和转录组改变情况,我们重新分析了来自癌症基因组图谱的公开数据。在约11000名患者和31种肿瘤类型中研究了影响整合子亚基基因的体细胞突变及其转录谱。观察到突变频率存在普遍异质性,主要取决于肿瘤类型。尽管我们无法将它们确定为癌症驱动基因,但某些基因在特定癌症中高度突变。对配对(正常和肿瘤)样本的转录组分析表明,在几种癌症中,[具体基因1]、[具体基因2]和[具体基因3]的转录有显著改变。对原发性肿瘤进行的实验验证证实了这些发现。