Identification and validation of plasma AGRN as a novel diagnostic biomarker of hepatitis B Virus-related chronic hepatitis and liver fibrosis/cirrhosis.

IF 2.5 4区 生物学 Q3 CELL BIOLOGY
Histology and histopathology Pub Date : 2024-08-01 Epub Date: 2023-12-21 DOI:10.14670/HH-18-695
Rong Ai, Lu Li, Xiwei Yuan, Dandan Zhao, Tongguo Miao, Weiwei Guan, Shiming Dong, Chen Dong, Yao Dou, Mengmeng Hou, Yuemin Nan
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引用次数: 0

Abstract

Objective: The aim of this study was to find novel biomarkers and develop a non-invasive, effective diagnostic model for hepatitis B Virus-related chronic hepatitis and liver fibrosis/cirrhosis.

Method: Quantitative real-time polymerase chain reaction (qRT-PCR) was utilized to assess the expression of differentially expressed genes (AGRN, JAG1, CCL5, ID3, CCND1, and CAPN2) in peripheral blood mononuclear cells (PBMCs) from healthy subjects, chronic hepatitis B (CHB), and liver fibrosis/cirrhosis (LF/LC) patients. The molecular mechanisms underlying AGRN-regulated CHB were further explored and verified in LX2 cells, in which small interfering RNA (siRNA) was used to block AGRN gene expression. Finally, enzyme-linked Immunosorbent Assay (ELISA) was used to measure AGRN protein expression in 100 healthy volunteers, 100 CHB patients, and 100 LF/LC patients, and the efficacy of the diagnostic model was assessed by the Area Under the Curve (AUC).

Results: AGRN mRNA displayed a steady rise in the PBMCs of normal, CHB, and LF/LC patients. Besides, AGRN expression was markedly elevated in activated LX2 cells, whereas the expression of COL1 and α-SMA decreased when AGRN was inhibited using siRNA. In addition, downregulation of AGRN can reduce the gene expression of β-catenin and c-MYC while upregulating the expression of GSK-3β. Furthermore, PLT and AGRN were used to develop a non-invasive diagnostic model (PA). To identify CHB patients from healthy subjects, the AUC of the PA model was 0.951, with a sensitivity of 87.0% and a specificity of 91.0%. The AUC of the PA model was 0.922 with a sensitivity of 82.0% and a specificity of 90.0% when differentiating between LF/LC and CHB patients.

Conclusion: The current study indicated that AGRN could be a potential plasma biomarker and the established PA model could improve the diagnostic accuracy for HBV-related liver diseases.

将血浆 AGRN 鉴定和验证为乙型肝炎病毒相关慢性肝炎和肝纤维化/肝硬化的新型诊断生物标记物。
研究目的本研究的目的是寻找新型生物标记物,并开发一种无创、有效的乙型肝炎病毒相关慢性肝炎和肝纤维化/肝硬化诊断模型:方法:利用定量实时聚合酶链反应(qRT-PCR)评估健康受试者、慢性乙型肝炎(CHB)和肝纤维化/肝硬化(LF/LC)患者外周血单核细胞(PBMCs)中差异表达基因(AGRN、JAG1、CCL5、ID3、CCND1 和 CAPN2)的表达情况。通过使用小干扰 RNA(siRNA)阻断 AGRN 基因的表达,在 LX2 细胞中进一步探索和验证了 AGRN 调节 CHB 的分子机制。最后,用酶联免疫吸附法(ELISA)检测了100名健康志愿者、100名CHB患者和100名LF/LC患者的AGRN蛋白表达,并用曲线下面积(AUC)评估了诊断模型的有效性:结果:AGRN mRNA在正常人、CHB患者和LF/LC患者的PBMC中呈稳定上升趋势。此外,AGRN 在活化的 LX2 细胞中表达明显升高,而当使用 siRNA 抑制 AGRN 时,COL1 和 α-SMA 的表达下降。此外,下调 AGRN 可降低 β-catenin 和 c-MYC 的基因表达,同时上调 GSK-3β 的表达。此外,PLT 和 AGRN 还被用于开发一种无创诊断模型(PA)。从健康受试者中鉴别出 CHB 患者,PA 模型的 AUC 为 0.951,灵敏度为 87.0%,特异度为 91.0%。在区分 LF/LC 和 CHB 患者时,PA 模型的 AUC 为 0.922,灵敏度为 82.0%,特异度为 90.0%:本研究表明,AGRN可能是一种潜在的血浆生物标志物,已建立的PA模型可提高对HBV相关肝病的诊断准确性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Histology and histopathology
Histology and histopathology 生物-病理学
CiteScore
3.90
自引率
0.00%
发文量
232
审稿时长
2 months
期刊介绍: HISTOLOGY AND HISTOPATHOLOGY is a peer-reviewed international journal, the purpose of which is to publish original and review articles in all fields of the microscopical morphology, cell biology and tissue engineering; high quality is the overall consideration. Its format is the standard international size of 21 x 27.7 cm. One volume is published every year (more than 1,300 pages, approximately 90 original works and 40 reviews). Each volume consists of 12 numbers published monthly online. The printed version of the journal includes 4 books every year; each of them compiles 3 numbers previously published online.
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