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富含亮氨酸重复序列LGI家族成员3:综合分析揭示其与非小细胞肺癌的预后关联。

Leucine rich repeat LGI family member 3: Integrative analyses reveal its prognostic association with non-small cell lung cancer.

作者信息

Kim Dong-Seok, Kwon Nyoun Soo, Yun Hye-Young

机构信息

Department of Biochemistry, Chung-Ang University, College of Medicine, Seoul 06974, Republic of Korea.

出版信息

Oncol Lett. 2019 Sep;18(3):3388-3398. doi: 10.3892/ol.2019.10648. Epub 2019 Jul 22.

Abstract

Leucine rich repeat LGI family member 3 (LGI3) is a member of the LGI protein family. Our previous studies reported that LGI3 was expressed in adipose tissues, brain and skin, where it served roles as a multifunctional cytokine and pro-inflammatory adipokine. It was hypothesized that LGI3 may be involved in cytokine networks in cancer. The present study aimed to analyze differentially expressed genes in non-small cell lung cancer (NSCLC) tissues and NSCLC cohort data, to evaluate the prognostic role of LGI3. Expression microarray and NSCLC cohort data were statistically analyzed by bioinformatic methods, and protein-protein interactions, functional enrichment and pathway, gene coexpression network (GCN) and prognostic association analyses were performed. The results demonstrated that the expression levels of LGI3 and its receptor a disintegrin and metalloproteinase domain-containing protein 22 were significantly decreased in NSCLC tissues. A total of two upregulated genes and 11 downregulated genes in NSCLC tissues were identified as LGI3-regulated genes. Protein-protein interaction network analysis demonstrated that all LGI3-regulated genes that were altered in NSCLC were involved in a protein-protein interaction network cluster. Functional enrichment, Kyoto Encyclopedia of Genes and Genomes pathway and GCN analyses demonstrated the association of these genes with the immune and inflammatory responses, angiogenesis, the tumor necrosis factor pathway, and chemokine and peroxisome proliferator-activated receptor signaling pathways. Analysis of NSCLC cohorts revealed that low expression levels of LGI3 was significantly associated with poor prognosis of NSCLC. Analysis of the somatic mutations of the LGI3 gene in NSCLC revealed that the amino acid residues altered in NSCLC included two single nucleotide polymorphism sites and three phylogenetically coevolved amino acid residues. Taken together, these results suggest that LGI3 may be a potential prognostic marker of NSCLC.

摘要

富含亮氨酸重复序列的LGI家族成员3(LGI3)是LGI蛋白家族的一员。我们之前的研究报道,LGI3在脂肪组织、脑和皮肤中表达,在这些组织中它作为一种多功能细胞因子和促炎脂肪因子发挥作用。据推测,LGI3可能参与癌症中的细胞因子网络。本研究旨在分析非小细胞肺癌(NSCLC)组织中的差异表达基因以及NSCLC队列数据,以评估LGI3的预后作用。通过生物信息学方法对表达微阵列和NSCLC队列数据进行统计学分析,并进行蛋白质-蛋白质相互作用、功能富集和通路、基因共表达网络(GCN)以及预后关联分析。结果表明,NSCLC组织中LGI3及其受体含去整合素和金属蛋白酶结构域蛋白22的表达水平显著降低。在NSCLC组织中总共鉴定出2个上调基因和11个下调基因作为LGI3调控基因。蛋白质-蛋白质相互作用网络分析表明,在NSCLC中发生改变的所有LGI3调控基因都参与了一个蛋白质-蛋白质相互作用网络簇。功能富集、京都基因与基因组百科全书通路和GCN分析表明这些基因与免疫和炎症反应、血管生成、肿瘤坏死因子通路以及趋化因子和过氧化物酶体增殖物激活受体信号通路相关。对NSCLC队列的分析显示,LGI3低表达与NSCLC的不良预后显著相关。对NSCLC中LGI3基因的体细胞突变分析表明,在NSCLC中发生改变的氨基酸残基包括两个单核苷酸多态性位点和三个系统发育上共同进化的氨基酸残基。综上所述,这些结果表明LGI3可能是NSCLC的一个潜在预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dfa/6704323/87ea1b0b2c5e/ol-18-03-3388-g00.jpg

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