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AGPAT5低表达与结直肠癌的临床分期及不良预后相关,并促进肿瘤进展。

Low Expression of AGPAT5 Is Associated With Clinical Stage and Poor Prognosis in Colorectal Cancer and Contributes to Tumour Progression.

作者信息

Zang Jia, Sun Juanjuan, Xiu WenChao, Liu Xiaoshuang, Chai Yunsheng, Zhou Yanyan

机构信息

Department of Colorectal Surgery, Shanghai Changzheng Hospital, Shanghai, P.R. China.

The Second Ward of Anorectal Department, Qilu Hospital of Shandong University (Qingdao), China.

出版信息

Clin Med Insights Oncol. 2022 Nov 30;16:11795549221137399. doi: 10.1177/11795549221137399. eCollection 2022.

Abstract

BACKGROUND

Colorectal cancer (CRC) has a high prevalence and poor prognosis. This study aimed to identify biomarkers related to the clinical stage (I-IV) of CRC.

METHODS

The LinkedOmics database was used as the discovery cohort, and two Gene Expression Omnibus (GEO) databases (GSE41258 and GSE422848) served as validation cohorts. The trend test of genes related to clinical stage (I-IV) of CRC patients was identified by the Jonckheere-Terpstra test. The cBioPortal database, Gene Expression Profiling Interactive Analysis (GEPIA) and PrognoScan databases were used to explore the expression change and prognostic value of clinical stage-related genes in CRC patients. CRC cells overexpressed AGPAT5 were constructed and used for cell counting kit-8 (CCK-8), flow cytometric, and wound healing assays in vitro.

RESULTS

We identified four clinical stage-related genes, GSR, AGPAT5, CRLF1, and NPR3, in CRC. The CNA frequencies of GSR, CRLF1, AGPAT5, and NPR3 occurred in 11%, 2.4%, 13%, and 3% of patients, respectively. The expression of GSR and AGPAT5 tended to decrease with CRC stage (I-IV) progression, and the expression of CRLF1 and NPR3 tended to increase with CRC stage (I-IV) progression. Compared with the normal group, AGPAT5 expression was markedly decreased in stage IV CRC. Higher GSR and AGPAT5 expression levels were associated with better overall survival (OS) and disease-free survival (DFS) in CRC patients. Lower CRLF1 and NPR3 expression levels were associated with better OS and DFS in CRC. GSR, CRLF1, AGPAT5, and NPR3 expression were related to CRC progression, microsatellite instability, and tumour purity in CRC. Furthermore, AGPAT5 was downregulated in CRC cell lines, and overexpression of AGPAT5 inhibited cell proliferation and migration and promoted cell apoptosis in CRC cells.

CONCLUSION

Low AGPAT5 expression may serve as a poor prognostic factor and clinical stage biomarker in CRC. In addition, AGPAT5 acts as a tumour suppressor in CRC progression.

摘要

背景

结直肠癌(CRC)患病率高且预后差。本研究旨在鉴定与CRC临床分期(I - IV期)相关的生物标志物。

方法

将LinkedOmics数据库用作发现队列,两个基因表达综合数据库(GEO)(GSE41258和GSE422848)用作验证队列。通过Jonckheere - Terpstra检验确定与CRC患者临床分期(I - IV期)相关基因的趋势检验。利用cBioPortal数据库、基因表达谱交互式分析(GEPIA)和PrognoScan数据库探讨CRC患者中临床分期相关基因的表达变化及预后价值。构建过表达AGPAT5的CRC细胞,并用于体外细胞计数试剂盒 - 8(CCK - 8)、流式细胞术和伤口愈合试验。

结果

我们在CRC中鉴定出四个与临床分期相关的基因,即GSR、AGPAT5、CRLF1和NPR3。GSR、CRLF1、AGPAT5和NPR3的拷贝数改变频率分别出现在11%、2.4%、13%和3%的患者中。GSR和AGPAT5的表达倾向于随CRC分期(I - IV期)进展而降低,CRLF1和NPR3的表达倾向于随CRC分期(I - IV期)进展而增加。与正常组相比,IV期CRC中AGPAT5表达明显降低。较高的GSR和AGPAT5表达水平与CRC患者更好的总生存期(OS)和无病生存期(DFS)相关。较低的CRLF1和NPR3表达水平与CRC患者更好的OS和DFS相关。GSR、CRLF,1、AGPAT5和NPR3的表达与CRC进展、微卫星不稳定性和肿瘤纯度相关。此外,AGPAT5在CRC细胞系中表达下调,AGPAT5过表达抑制CRC细胞增殖和迁移并促进细胞凋亡。

结论

低AGPAT5表达可能是CRC预后不良的因素和临床分期生物标志物。此外,AGPAT5在CRC进展中起肿瘤抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df78/9716453/c7b79c8e8216/10.1177_11795549221137399-fig1.jpg

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