Identification and analysis of key genes related to efferocytosis in colorectal cancer.

IF 2.1 4区 医学 Q3 GENETICS & HEREDITY BMC Medical Genomics Pub Date : 2024-08-06 DOI:10.1186/s12920-024-01967-8
Shengliang Zhang, Ying Jiang, Lei Shi, Tianning Wei, Zhiwen Lai, Xuan Feng, Shiyuan Li, Detao Tang
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引用次数: 0

Abstract

The impact of efferocytosis-related genes (ERGs) on the diagnosis of colorectal cancer (CRC) remains unclear. In this study, efferocytosis-associated biomarkers for the diagnosis of CRC were identified by integrating data from transcriptome sequencing and public databases. Finally, the expression of biomarkers was validated by real-time quantitative polymerase chain reaction (RT-qPCR). Our study may provide a reference for CRC diagnosis.

Background: It has been shown that some efferocytosis related genes (ERGs) are associated with the development of cancer. However, it is still uncertain how ERGs may influence the diagnosis of colorectal cancer (CRC).

Methods: In our study, the CRC cohorts were gained from transcriptome sequencing and the gene expression omnibus (GEO) database (GSE71187). Efferocytosis related biomarkers with diagnostic utility for CRC were identified through combining differentially expressed analysis, machine learning algorithms, and receiver operating characteristic (ROC) analysis. Then, infiltration abundance of immune cells between CRC and control was evaluated. The regulatory networks (including mRNA-miRNA-lncRNA and miRNA/transcription factors (TF)-mRNA networks) were created. Finally, the expression of biomarkers was validated via real-time quantitative polymerase chain reaction (RT-qPCR).

Results: There were 3 biomarkers (ELMO3, P2RY12, and PDK4) related diagnosis for CRC patients gained. ELMO3 was highly expressed in CRC group, while P2RY12 and PDK4 was lowly expressed. Besides, the infiltrating abundance of 3 immune cells between CRC and control groups was significantly differential, namely activated CD4 memory T cells, macrophages M0, and resting mast cells. We then constructed a mRNA-miRNA-lncRNA network containing 3 mRNAs, 33 miRNAs, and 22 lncRNAs, and a miRNA/TF-mRNA network including 3 mRNAs, 33 miRNAs, and 7 TFs. Additionally, RT-qPCR results revealed that the expression trends of all biomarkers were consistent with the transcriptome sequencing data and GSE71187.

Conclusion: Taken together, this study provides three efferocytosis related biomarkers (ELMO3, P2RY12, and PDK4) for diagnosis of CRC, providing a scientific reference for further studies of CRC.

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鉴定和分析结直肠癌流出细胞相关的关键基因。
排泄相关基因(ERGs)对结直肠癌(CRC)诊断的影响尚不清楚。在这项研究中,通过整合转录组测序和公共数据库的数据,确定了用于诊断 CRC 的与排泄相关的生物标志物。最后,通过实时定量聚合酶链反应(RT-qPCR)验证了生物标志物的表达。我们的研究可为 CRC 诊断提供参考:背景:已有研究表明,一些与排泄相关的基因(ERGs)与癌症的发生有关。背景:已有研究表明,一些与排泄相关的基因(ERGs)与癌症的发生有关,但ERGs如何影响结直肠癌(CRC)的诊断仍不确定:在我们的研究中,CRC 队列来自转录组测序和基因表达总库(GEO)数据库(GSE71187)。通过结合差异表达分析、机器学习算法和接收者操作特征(ROC)分析,确定了对 CRC 有诊断作用的胞吐相关生物标记物。然后评估了 CRC 和对照组之间免疫细胞的浸润丰度。建立了调控网络(包括mRNA-miRNA-lncRNA和miRNA/转录因子(TF)-mRNA网络)。最后,通过实时定量聚合酶链反应(RT-qPCR)验证了生物标志物的表达:结果:有 3 个生物标记物(ELMO3、P2RY12 和 PDK4)与 CRC 患者的诊断相关。ELMO3 在 CRC 组中高表达,而 P2RY12 和 PDK4 低表达。此外,3种免疫细胞的浸润丰度在 CRC 组和对照组之间存在显著差异,即活化的 CD4 记忆 T 细胞、巨噬细胞 M0 和静息肥大细胞。随后,我们构建了一个包含 3 个 mRNA、33 个 miRNA 和 22 个 lncRNA 的 mRNA-miRNA-lncRNA 网络,以及一个包含 3 个 mRNA、33 个 miRNA 和 7 个 TF 的 miRNA/TF-mRNA 网络。此外,RT-qPCR结果显示,所有生物标志物的表达趋势与转录组测序数据和GSE71187一致:综上所述,本研究为诊断 CRC 提供了三个与流出细胞相关的生物标记物(ELMO3、P2RY12 和 PDK4),为进一步研究 CRC 提供了科学参考。
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来源期刊
BMC Medical Genomics
BMC Medical Genomics 医学-遗传学
CiteScore
3.90
自引率
0.00%
发文量
243
审稿时长
3.5 months
期刊介绍: BMC Medical Genomics is an open access journal publishing original peer-reviewed research articles in all aspects of functional genomics, genome structure, genome-scale population genetics, epigenomics, proteomics, systems analysis, and pharmacogenomics in relation to human health and disease.
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