Four potential prognostic markers for breast cancer identified by hybrid gene and module expression analysis

Lin Xi, Xiangyang Yuan, Jing Liu, X. Tang
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Abstract

With the aim of screening the prognostic genes for breast cancer (BRCA) and exploring the possible mechanism and clinical value of these genes in the growth and regression stage of disease, we study the genes in the public gene expression omnibus (GEO) GSE22820 and the cancer genome atlas (TCGA). To achieve high-confidence gene candidates for BRCA, we present a hybrid gene and module analysis pipeline that strategically considers data mining on different datasets. Ultimately, four gene candidates, i.e., PLIN1, GPD1, LIPE, and CHRDL1, are targeted for BRCA. Afterwards, Kaplan-Meier survival analysis is performed on these genes for verification, revealing that the overall survival time of patients with low expression of these genes was shorter than that of patients with high expression (with P<0.05). Moreover, in order to study the role of these genes in the mechanisms and functionality related to cytoplasmic lipid metabolism, functional enrichment and pathway analysis are implemented. The results indicate that the expression of the four discovered genes plays an adverse role in BRCA development and could serve as effective biomarkers for predicting the formation and progression of BRCA.
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通过杂交基因和模块表达分析确定乳腺癌的四个潜在预后标志物
为了筛选乳腺癌(BRCA)的预后基因,探讨这些基因在疾病生长和消退阶段的可能机制和临床价值,我们研究了公共基因表达图谱(GEO) GSE22820和癌症基因组图谱(TCGA)中的基因。为了获得高可信度的BRCA候选基因,我们提出了一种混合基因和模块分析管道,该管道战略性地考虑了对不同数据集的数据挖掘。最终,四个候选基因PLIN1、GPD1、LIPE和CHRDL1成为BRCA的靶点。随后对这些基因进行Kaplan-Meier生存分析验证,发现这些基因低表达患者的总生存时间短于高表达患者(P<0.05)。此外,为了研究这些基因在细胞质脂代谢相关机制和功能中的作用,我们进行了功能富集和途径分析。结果表明,这四个基因的表达在BRCA的发生发展中起着不利的作用,可以作为预测BRCA形成和进展的有效生物标志物。
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