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通过生物信息学分析,预期这些潜在的关键基因将成为结直肠癌早期诊断的生物标志物。

Potential key genes are expected to become biomarker for early diagnosis of colorectal cancer through bioinformatics analysis.

机构信息

Department of Gastrointestinal Surgery, The second Affiliated Hospital of Shandong First Medical University, Tai'an, China.

Department of Rehabilitation, Taishan Vocational College of Nursing, Tai'an, China.

出版信息

Biotechnol Genet Eng Rev. 2024 Apr;40(1):678-691. doi: 10.1080/02648725.2023.2186586. Epub 2023 Mar 7.

Abstract

Colorectal cancer (CRC) is the leading cause of cancer-related deaths in the world. The aim of this study was to identify the potential key genes, and associated pathways for early-onset CRC through bioinformatics methods. We integrated the gene expression patterns of CRC from three RNAseq datasets (GSE8671, GSE20916, GSE39582) from GEO database to identify DEGs between CRC and normal samples. We established a gene co-expression network through WGCNA. Through the WGCNA calculation, the genes were divided into six modules. The WGCNA analysis screened 242 genes associated with pathological stage and colorectal adenocarcinoma, 31 of which had the ability to predict OS with an AUC >0.7. The GSE39582 dataset identified 2040 DEGs between the CRC and normal samples. The two were intersected to obtain two genes: NPM1 and PANK3. The two genes were used as a threshold to divide the samples into high group and low group for survival analysis. Survival analysis showed that increased expression of both genes was significantly associated with a poorer prognosis. These two genes (NPM1 and PANK3) could be possible marker genes for early diagnosis of CRC, providing ideas for other experimental studies in the future.

摘要

结直肠癌(CRC)是全球癌症相关死亡的主要原因。本研究旨在通过生物信息学方法鉴定早发性 CRC 的潜在关键基因和相关途径。我们整合了 GEO 数据库中三个 RNAseq 数据集(GSE8671、GSE20916、GSE39582)中来自 CRC 的基因表达模式,以鉴定 CRC 与正常样本之间的差异表达基因。我们通过 WGCNA 建立了基因共表达网络。通过 WGCNA 计算,将基因分为六个模块。WGCNA 分析筛选出 242 个与病理分期和结直肠腺癌相关的基因,其中 31 个基因具有 AUC>0.7 的 OS 预测能力。GSE39582 数据集鉴定出 CRC 和正常样本之间的 2040 个差异表达基因。将两者相交,得到两个基因:NPM1 和 PANK3。将这两个基因作为阈值将样本分为高组和低组进行生存分析。生存分析表明,这两个基因(NPM1 和 PANK3)的表达增加与预后不良显著相关。这两个基因(NPM1 和 PANK3)可能是 CRC 早期诊断的潜在标记基因,为未来的其他实验研究提供了思路。

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