Qin Xin-Gan, Zeng Jiang-Hui, Lin Peng, Mo Wei-Jia, Li Qing, Feng Zhen-Bo, Luo Dian-Zhong, Yang Hong, Chen Gang, Zeng Jing-Jing
Department of Gastrointestinal Surgery, First Affiliated Hospital of Guangxi Medical University, Guangxi Zhuang Autonomous Region 530021, Nanning, PR China.
Department of Pathology, First Affiliated Hospital of Guangxi Medical University, Guangxi Zhuang Autonomous Region 530021, Nanning, PR China.
Pathol Res Pract. 2019 Mar;215(3):414-426. doi: 10.1016/j.prp.2018.11.004. Epub 2018 Nov 10.
Malignant tumors of the digestive tract include esophageal, gastric, and colorectal carcinomas, which all have high global mortality rates. A clinical role for small nuclear RNA (snRNA), a type of small non-coding RNA, has not yet been documented for digestive tract pan-adenocarcinomas. Therefore, the aim of the study was to identify differentially expressed snRNAs and to explore their prognostic implications in pan-adenocarcinomas from the esophagus, stomach, colon, and rectum. The pan-carcinoma RNA-sequencing data of four types of digestive tract cancers with 1, 102 cases obtained from The Cancer Genome Atlas (TCGA) project were analyzed and the differentially expressed snRNAs were evaluated using the edgeR package. The prognostic value of each of the selected snRNAs was determined by univariate and multivariate Cox regression analyses. All the digestive tract pan-adenocarcinomas showed differential expression of three snRNAs: the up-regulated RNU1-106 P and RNU6-850 P and the down-regulated RNU6-529 P. Interestingly, RNU6-101 P appeared to be a risk factor for esophageal adenocarcinoma (ESAD) and RNVU1-4 was potentially a protective factor for stomach adenocarcinoma (STAD) survival. This consistent finding of differential expression of all three snRNAs in all four types of digestive system cancers suggests potential roles for these snRNAs in the tumorigenesis of digestive system cancers. RNU6-101 P could play a pivotal role in the progression of ESAD and RNVU1-4 could perform a protective role in STAD. However, since the current findings were based on RNA-sequencing data mining, more studies are needed for verification.
消化道恶性肿瘤包括食管癌、胃癌和结直肠癌,这些肿瘤在全球的死亡率都很高。小核RNA(snRNA)是一种小的非编码RNA,其在消化道泛腺癌中的临床作用尚未见报道。因此,本研究的目的是鉴定差异表达的snRNA,并探讨它们在食管、胃、结肠和直肠泛腺癌中的预后意义。分析了从癌症基因组图谱(TCGA)项目获得的1102例四种消化道癌症的泛癌RNA测序数据,并使用edgeR软件包评估差异表达的snRNA。通过单变量和多变量Cox回归分析确定每个选定snRNA的预后价值。所有消化道泛腺癌均显示三种snRNA的差异表达:上调的RNU1-106 P和RNU6-850 P以及下调的RNU6-529 P。有趣的是,RNU6-101 P似乎是食管腺癌(ESAD)的危险因素,而RNVU1-4可能是胃腺癌(STAD)生存的保护因素。在所有四种消化系统癌症中均一致发现这三种snRNA的差异表达,这表明这些snRNA在消化系统癌症的肿瘤发生中可能发挥作用。RNU6-101 P可能在ESAD的进展中起关键作用,而RNVU1-4可能在STAD中发挥保护作用。然而,由于目前的发现基于RNA测序数据挖掘,因此需要更多的研究来进行验证。