Chi Xiao-Jv, Song Yi-Bei, Liu Deng-He, Wei Li-Qiang, An Xin, Feng Zi-Zhen, Lan Xiao-Hua, Lan Dong, Huang Chao
Department of Clinical Laboratory, The First Affiliated Hospital of Guangxi Medical University, Key Laboratory of Clinical Laboratory Medicine of Guangxi Department of Education, Nanning, China.
The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Digit Health. 2023 Sep 26;9:20552076231203902. doi: 10.1177/20552076231203902. eCollection 2023 Jan-Dec.
Although surgical methods are the most effective treatments for colon adenocarcinoma (COAD), the cure rates remain low, and recurrence rates remain high. Furthermore, platelet adhesion-related genes are gaining attention as potential regulators of tumorigenesis. Therefore, identifying the mechanisms responsible for the regulation of these genes in patients with COAD has become important. The present study aims to investigate the underlying mechanisms of platelet adhesion-related genes in COAD patients.
The present study was an experimental study. Initially, the effects of platelet number and related genomic alteration on survival were explored using real-world data and the cBioPortal database, respectively. Then, the differentially expressed platelet adhesion-related genes of COAD were analyzed using the TCGA database, and patients were further classified by employing the non-negative matrix factorization (NMF) analysis method. Afterward, some of the clinical and expression characteristics were analyzed between clusters. Finally, least absolute shrinkage and selection operator regression analysis was used to establish the prognostic nomogram. All data analyses were performed using the R package.
High platelet counts are associated with worse survival in real-world patients, and alternations to platelet adhesion-related genes have resulted in poorer prognoses, based on online data. Based on platelet adhesion-related genes, patients with COAD were classified into two clusters by NMF-based clustering analysis. Cluster2 had a better overall survival, when compared to Cluster1. The gene copy number and enrichment analysis results revealed that two pathways were differentially enriched. In addition, the differentially expressed genes between these two clusters were enriched for POU6F1 in the transcription factor signaling pathway, and for MATN3 in the ceRNA network. Finally, a prognostic nomogram, which included the ALOX12 and ACTG1 genes, was established based on the platelet adhesion-related genes, with a concordance (C) index of 0.879 (0.848-0.910).
The mRNA expression-based NMF was used to reveal the potential role of platelet adhesion-related genes in COAD. The series of experiments revealed the feasibility of targeting platelet adhesion-associated gene therapy.
尽管手术方法是治疗结肠腺癌(COAD)最有效的手段,但治愈率仍然较低,复发率仍然较高。此外,血小板黏附相关基因作为肿瘤发生的潜在调节因子正受到关注。因此,确定COAD患者中这些基因的调控机制变得至关重要。本研究旨在探讨COAD患者中血小板黏附相关基因的潜在机制。
本研究为实验性研究。首先,分别使用真实世界数据和cBioPortal数据库探讨血小板数量和相关基因组改变对生存的影响。然后,使用TCGA数据库分析COAD中差异表达的血小板黏附相关基因,并采用非负矩阵分解(NMF)分析方法对患者进行进一步分类。之后,分析各聚类之间的一些临床和表达特征。最后,使用最小绝对收缩和选择算子回归分析建立预后列线图。所有数据分析均使用R包进行。
基于在线数据,在真实世界患者中,高血小板计数与较差的生存相关,血小板黏附相关基因的改变导致预后更差。基于血小板黏附相关基因,通过基于NMF的聚类分析将COAD患者分为两个聚类。与聚类1相比,聚类2的总生存期更好。基因拷贝数和富集分析结果显示两条通路存在差异富集。此外,这两个聚类之间的差异表达基因在转录因子信号通路中富集于POU6F1,在ceRNA网络中富集于MATN3。最后,基于血小板黏附相关基因建立了包含ALOX12和ACTG1基因的预后列线图,一致性(C)指数为0.879(0.848 - 0.910)。
基于mRNA表达的NMF用于揭示血小板黏附相关基因在COAD中的潜在作用。一系列实验揭示了靶向血小板黏附相关基因治疗的可行性。