Zhao Zi-Tong, Li Yang, Yuan Hong-Yu, Ma Fu-Hai, Song Yong-Mei, Tian Yan-Tao
State Key Laboratory of Molecular Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Department of Pancreatic and Gastric Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
World J Clin Cases. 2020 Feb 26;8(4):658-669. doi: 10.12998/wjcc.v8.i4.658.
Gastric signet ring cell carcinoma (GSRCC) is one of the most malignant tumors. It has the features of high invasiveness, rapid progression, and resistance to chemotherapy. However, systematic analyses of mRNAs have not yet been performed for GSRCC.
To identify key mRNAs and signaling pathways in GSRCC.
A transcriptome analysis of two GSRCC and two non-GSRCC samples was performed in this study. Differentially expressed mRNAs and pathways were identified based on the KEGG and PANTHER pathway annotations. The interactive relationships among the differential genes were mapped with the STRING database. Quantitative real-time polymerase chain reaction was used to validate the key gene expression in GSRCC.
About 1162 differential genes (using a 2-fold cutoff, < 0.05) were identified in GSRCC compared with non-GSRCC. The enriched KEGG and PANTHER pathways for the differential genes included immune response pathways, metabolic pathways, and metastasis-associated pathways. Ten genes (, , , , , , , , , and ) were identified as hub genes in the protein-protein interaction network. The expression levels of five genes (, , , , and ) showed potential clinical value.
We have identified the potential key genes and pathways in GSRCC, and these hub genes and pathways could be diagnostic markers and therapeutic targets for GSRCC.
胃印戒细胞癌(GSRCC)是最恶性的肿瘤之一。它具有高侵袭性、进展迅速和对化疗耐药的特点。然而,尚未对GSRCC进行mRNA的系统分析。
鉴定GSRCC中的关键mRNA和信号通路。
本研究对两个GSRCC样本和两个非GSRCC样本进行了转录组分析。基于KEGG和PANTHER通路注释鉴定差异表达的mRNA和通路。利用STRING数据库绘制差异基因之间的相互作用关系。采用定量实时聚合酶链反应验证GSRCC中关键基因的表达。
与非GSRCC相比,GSRCC中鉴定出约1162个差异基因(采用2倍截断值,<0.05)。差异基因富集的KEGG和PANTHER通路包括免疫反应通路、代谢通路和转移相关通路。在蛋白质-蛋白质相互作用网络中鉴定出10个基因(,,,,,,,,,和)作为枢纽基因。5个基因(,,,,和)的表达水平显示出潜在的临床价值。
我们已经鉴定出GSRCC中的潜在关键基因和通路,这些枢纽基因和通路可能成为GSRCC的诊断标志物和治疗靶点。