Volume 132, Issue 7 pp. 507-514
Original Article

LncRNA SNHG1 serves as a biomarker for systemic lupus erythematosus and participates in the disease progression

Linsen Jiang

Linsen Jiang

Department of Nephrology, The Second Affiliated Hospital of Soochow University, Suzhou, China

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Anning Qi

Anning Qi

Department of Laboratory, Nanjing LuHe People’s Hospital, Nanjing, China

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Hongyu Yang

Hongyu Yang

Department of Clinical Laboratory, Affiliated Hospital of PanZhiHua University, Panzhihua, China

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Shuping Wang

Corresponding Author

Shuping Wang

Department of Clinical Laboratory, Affiliated Hospital of PanZhiHua University, Panzhihua, China

Shuping Wang, Department of Clinical Laboratory, Affiliated Hospital of PanZhiHua University, No.27 Taoyuan Street, Bingcaogang, East District, Panzhihua City, Sichuan Province 617000, China. e-mail: [email protected]

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Fei Wang

Fei Wang

Department of Clinical Laboratory, Affiliated Hospital of PanZhiHua University, Panzhihua, China

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Xuemei Bai

Xuemei Bai

Department of Clinical Laboratory, Affiliated Hospital of PanZhiHua University, Panzhihua, China

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Juan Ren

Juan Ren

Department of Clinical Laboratory, Affiliated Hospital of PanZhiHua University, Panzhihua, China

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First published: 21 April 2024
Citations: 1

Linsen Jiang and Anning Qi should be considered joint first author.

Abstract

LncRNAs play an important role in autoimmune diseases. The purpose of this study was to explore the role of lncRNA SNHG1 in systemic lupus erythematosus (SLE), and laid a theoretical foundation for the study of SLE. The basic clinical information of all subjects was first collected for statistical analysis, and SNHG1 expression in the serum of all subjects was detected by RT-qPCR. The value of SNHG1 in the diagnosis of SLE was assessed by ROC. The correlation between SNHG1 and each blood sample index was analyzed by Pearson correlation analysis. The role of SNHG1 in primary peripheral blood mononuclear cells (PBMCs) apoptosis was explored. SNHG1 expression is relatively upregulated in patients with SLE compared to healthy people. SNHG1 expression was positively correlated with SLEDAI score, IgG, CRP, and ESR, and negatively correlated with C3 and C4. ROC indicated that SNHG1 has the potential to assist in the diagnosis of SLE. PBMCs apoptosis in SLE was higher than that in control group, the knockdown and overexpression of SNHG1 could correspondingly inhibit and promote PBMCs apoptosis. SNHG1 has the potential to be a diagnosis marker for SLE and may be involved in regulating PBMCs apoptosis.

CONFLICT OF INTEREST

The authors declare that they have no competing interests.

DATA AVAILABILITY STATEMENT

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

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