CLEC1B is a Promising Prognostic Biomarker and Correlated with Immune Infiltration in Hepatocellular Carcinoma.

IF 2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL International Journal of General Medicine Pub Date : 2022-06-16 eCollection Date: 2022-01-01 DOI:10.2147/IJGM.S363050
Xiaoliang Liang, Fei Song, Wanzhi Fang, Yu Zhang, Zihan Feng, Zeyin Chen, Lu Han, Zhong Chen
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引用次数: 2

Abstract

Purpose: C-type lectin domain family 1 member B (CLEC1B) is a protein-coding gene involved in various processes, such as platelet activation, tumor cell metastasis and separation of blood/lymphatic vessels. However, how CLEC1B plays its role in hepatocellular carcinoma (HCC) has not been well studied. The purpose of this study was to investigate the clinical significance and biological function of CLEC1B in HCC.

Patients and methods: Based on (The Cancer Genome Atlas) TCGA database, CLEC1B expression matrix and corresponding clinical information were extracted. ROC curves and Kaplan-Meier method were generated to evaluate the value of CLEC1B as a diagnostic and prognostic biomarker. Moreover, single-gene difference analysis constructed by DESeq2 method and then the related genes were used to predict CLEC1B-related signaling pathways. The ssGSEA algorithm was conducted for studies related to immune infiltration. CLEC1B protein expression was evaluated and immunohistochemistry in HCC tissues through tissue microarray. Finally, the relationship between CLEC1B expression and T cell infiltration was assessed according to tissue microarray.

Results: The mRNA and protein levels of CLEC1B were significantly down-regulated in HCC compared to paired normal tissues, which were further verified in clinical tissue samples. ROC curves and Kaplan-Meier survival analysis suggested the significant diagnostic and clinical prognostic value of CLEC1B. Meanwhile, downregulation of CLEC1B was significantly associated with clinical parameters such as clinical tumor vascular invasion and distant metastasis. Moreover, Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG) and gene set enrichment (GSEA) analysis indicated that CLEC1B has significant association with immune function. Finally, immune infiltration analysis indicated that CLEC1B was significantly associated with immune cell subsets and affected the efficacy of immunotherapy in cancer patient.

Conclusion: Collectively, our findings suggested that CLEC1B could be a promising prognostic biomarker in HCC and its expression was related to immune cell infiltration.

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CLEC1B是一种很有前景的预后生物标志物,与肝细胞癌的免疫浸润有关。
目的:c型凝集素结构域家族1成员B (CLEC1B)是一种参与血小板活化、肿瘤细胞转移、血/淋巴管分离等多种过程的蛋白编码基因。然而,cle1b如何在肝细胞癌(HCC)中发挥作用尚未得到很好的研究。本研究旨在探讨CLEC1B在HCC中的临床意义及生物学功能。患者和方法:基于(The Cancer Genome Atlas) TCGA数据库,提取cle1b表达矩阵及相应的临床信息。生成ROC曲线和Kaplan-Meier法来评估cle1b作为诊断和预后生物标志物的价值。此外,利用DESeq2方法构建单基因差异分析,然后利用相关基因预测cle1b相关信号通路。针对免疫浸润相关的研究,采用ssGSEA算法。通过组织芯片技术检测cle1b蛋白在HCC组织中的表达及免疫组化。最后,通过组织芯片检测CLEC1B表达与T细胞浸润的关系。结果:与配对的正常组织相比,HCC中CLEC1B mRNA和蛋白水平明显下调,这在临床组织样本中得到进一步验证。ROC曲线和Kaplan-Meier生存分析提示cle1b具有重要的诊断和临床预后价值。同时,CLEC1B下调与临床肿瘤血管侵袭、远处转移等临床参数有显著相关性。此外,基因本体(GO)、京都基因与基因组百科全书(KEGG)和基因集富集(GSEA)分析表明,cle1b与免疫功能有显著关联。最后,免疫浸润分析提示cleec1b与肿瘤患者免疫细胞亚群显著相关,影响免疫治疗效果。结论:综上所述,我们的研究结果表明,CLEC1B可能是HCC中有希望的预后生物标志物,其表达与免疫细胞浸润有关。
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来源期刊
International Journal of General Medicine
International Journal of General Medicine Medicine-General Medicine
自引率
0.00%
发文量
1113
审稿时长
16 weeks
期刊介绍: The International Journal of General Medicine is an international, peer-reviewed, open access journal that focuses on general and internal medicine, pathogenesis, epidemiology, diagnosis, monitoring and treatment protocols. The journal is characterized by the rapid reporting of reviews, original research and clinical studies across all disease areas. A key focus of the journal is the elucidation of disease processes and management protocols resulting in improved outcomes for the patient. Patient perspectives such as satisfaction, quality of life, health literacy and communication and their role in developing new healthcare programs and optimizing clinical outcomes are major areas of interest for the journal. As of 1st April 2019, the International Journal of General Medicine will no longer consider meta-analyses for publication.
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