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基于转录组测序和生物信息学分析鉴定肠化生的潜在致病基因

[Identification of potential pathogenic genes of intestinal metaplasia based on transcriptomic sequencing and bioinformatics analysis].

作者信息

Pei B, Zhang Y, Wei S, Mei Y, Song B, Dong G, Wen Z, Li X

机构信息

Second Affiliated Hospital of Anhui University of Chinese Medicine, Anhui 230000, China.

First Clinical Medical College of Nanjing Medical University, Nanjing 210000, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2024 May 20;44(5):941-949. doi: 10.12122/j.issn.1673-4254.2024.05.16.

Abstract

OBJECTIVE

To explore the potential pathogenic genes of intestinal metaplasia.

METHODS

Twenty-one patients with intestinal metaplasia admitted to the Department of Gastroenterology at the Second Affiliated Hospital of Anhui University of Chinese Medicine from January, 2022 to June, 2022, and 21 healthy subjects undergoing gastroscopic examination during the same period were enrolled in this study. All the participants underwent gastroscopy and pathological examination, and gastric tissue samples were collected for transcriptome sequencing to screen for differentially expressed genes (DEGs). The biological functions of the DEGs were analyzed using bioinformatics analysis, and qRT-PCR was used to validate the results.

RESULTS

Transcriptomic sequencing identified a total of 1373 DEGs, including 827 upregulated and 546 downregulated ones. The top 6 upregulated genes (, , , , , and ), ranked based on their significance and average expression level, were selected for validation, and qRT-PCR showed significant upregulation of their mRNAs in the gastric tissues of patients with intestinal metaplasia ( < 0.05).

CONCLUSION

, , , , , and participate in the occurrence and development of intestinal metaplasia, and may serve as potential biomarkers for diagnosing intestinal metaplasia.

摘要

目的

探索肠化生的潜在致病基因。

方法

选取2022年1月至2022年6月安徽中医药大学第二附属医院收治的21例肠化生患者以及同期接受胃镜检查的21例健康受试者纳入本研究。所有参与者均接受胃镜检查及病理检查,并采集胃组织样本进行转录组测序以筛选差异表达基因(DEGs)。采用生物信息学分析方法分析DEGs的生物学功能,并通过qRT-PCR验证结果。

结果

转录组测序共鉴定出1373个DEGs,其中上调基因827个,下调基因546个。根据其显著性和平均表达水平,选取上调最显著的前6个基因(、、、、、)进行验证,qRT-PCR结果显示这些基因的mRNA在肠化生患者胃组织中显著上调(<0.05)。

结论

、、、、、参与肠化生的发生发展过程,可能作为诊断肠化生的潜在生物标志物。

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