Ye M, Wu H, Mei Y, Zhang Q
School of Medicine, South China University of Technology, Guangzhou 510006, China.
Department of Pathology, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, Guangzhou 510080, China.
Nan Fang Yi Ke Da Xue Xue Bao. 2024 Sep 20;44(9):1776-1782. doi: 10.12122/j.issn.1673-4254.2024.09.18.
To analyze the expression of CREM in gastric cancer (GC) and its correlation with prognosis of the patients.
TCGA and GEO databases were used to analyze the expression levels of CREM mRNA in GC and adjacent tissues. Immunohistochemistry was used to examine the expression of CREM protein in 43 pairs of GC and adjacent tissues, and the correlation of CREM expression with clinicopathological features of the patients was analyzed. Kaplan-Meier survival analysis was used to explore the relationship between CREM expression and survival of GC patients. LinkedOmics database was used to annotate the GO function and KEGG pathway enrichment of CREM-related genes.
Database analysis showed that CREM was highly expressed in GC tissues ( < 0.05) and positively correlated with poor prognosis in GC patients (=0.01). Immunohistochemistry results showed significantly higher CREM expression in GC tissues than in paired adjacent tissues ( < 0.0001), and its expression level was correlated with T-stage and N-stage of the tumor ( < 0.05). The overall survival of GC patients with high expression of CREM was shorter (=4.02, =0.0046). Gene enrichment analysis showed that high CREM expression promotes occurrence and progression of GC very likely through the cell adhesion signaling pathway.
CREM is highly expressed in GC, and its high expression is associated with a poor prognosis of GC patients, suggesting the potential of CREM to serve as a prognostic indicator for GC.
分析胃癌(GC)中CREM的表达及其与患者预后的相关性。
利用TCGA和GEO数据库分析GC组织及癌旁组织中CREM mRNA的表达水平。采用免疫组织化学法检测43对GC组织及癌旁组织中CREM蛋白的表达情况,并分析CREM表达与患者临床病理特征的相关性。采用Kaplan-Meier生存分析法探讨CREM表达与GC患者生存的关系。利用LinkedOmics数据库对CREM相关基因进行GO功能注释和KEGG通路富集分析。
数据库分析显示,CREM在GC组织中高表达(<0.05),且与GC患者的不良预后呈正相关(=0.01)。免疫组织化学结果显示,GC组织中CREM表达明显高于配对的癌旁组织(<0.0001),其表达水平与肿瘤的T分期和N分期相关(<0.05)。CREM高表达的GC患者总生存期较短(=4.02,=0.0046)。基因富集分析表明,CREM高表达很可能通过细胞黏附信号通路促进GC的发生和进展。
CREM在GC中高表达,其高表达与GC患者预后不良相关,提示CREM有望作为GC的预后指标。