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We are analyzing https://link.springer.com/article/10.1186/s13075-024-03356-z.

Title:
Investigation of ferroptosis-associated molecular subtypes and immunological characteristics in lupus nephritis based on artificial neural network learning | Arthritis Research & Therapy
Description:
Background Lupus nephritis (LN) is a severe complication of systemic lupus erythematosus (SLE) with poor treatment outcomes. The role and underlying mechanisms of ferroptosis in LN remain largely unknown. We aimed to explore ferroptosis-related molecular subtypes and assess their prognostic value in LN patients. Methods Molecular subtypes were classified on the basis of differentially expressed ferroptosis-related genes (FRGs) via the Consensus ClusterPlus package. The enriched functions and pathways, immune infiltrating levels, immune scores, and immune checkpoints were compared between the subgroups. A scoring algorithm based on the subtype-specific feature genes identified by artificial neural network machine learning, referred to as the NeuraLN, was established, and its immunological features, clinical value, and predictive value were evaluated in patients with LN. Finally, immunohistochemical analysis was performed to validate the expression and role of feature genes in glomerular tissues from LN patients and controls. Results A total of 10 differentially expressed FRGs were identified, most of which showed significant correlation. Based on the 10 FRGs, LN patients were classified into two ferroptosis subtypes, which exhibited significant differences in immune cell abundances, immune scores, and immune checkpoint expression. A NeuraLN-related protective model was established based on nine subtype-specific genes, and it exhibited a robustly predictive value in LN. The nomogram and calibration curves demonstrated the clinical benefits of the protective model. The high-NeuraLN group was closely associated with immune activation. Clinical specimens demonstrated the alterations of ALB, BHMT, GAMT, GSTA1, and HAO2 were in accordance with bioinformatics analysis results, GSTA1 and BHMT were negatively correlated with the severity of LN. Conclusion The classification of ferroptosis subtypes and the establishment of a protective model may form a foundation for the personalized treatment of LN patients.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {๐Ÿ“š}

  • Science
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Content Management System {๐Ÿ“}

What CMS is link.springer.com built with?

Custom-built

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Traffic Estimate {๐Ÿ“ˆ}

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๐ŸŒ  Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,019 visitors per month in the current month.
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How Does Link.springer.com Make Money? {๐Ÿ’ธ}

We don't see any clear sign of profit-making.

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Keywords {๐Ÿ”}

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Topics {โœ’๏ธ}

atg5-atg7-ncoa4and p62-keap1-nrf2 axis p53-sat1-alox15-dependent lipid pathways streptavidinโ€“biotin-peroxidase conjugate b-cell targeting therapy bhmt-dependent methylation pathway article download pdf fatty acid beta-oxidation rabbit anti-bhmt antibody rabbit anti-alb antibody rabbit anti-hao2 antibody rabbit anti-dpys antibody rabbit anti-pah antibody rabbit anti-cubn antibody rabbit anti-slc27a2 antibody rabbit anti-gsta1 antibody rabbit anti-gamt antibody systemic lupus erythematosus sections underwent counter-staining ferroptosis-related molecular markers er stress-independent ferroptosis single-cell rna sequencing hub ferroptosis-related genes neuraln-related protective model multi-center ln cohort glutathione transferase a1 mitigating lipid peroxidation metabolism-related signaling pathway ferroptosis-related molecular subtypes immune-related signaling pathways iron-catalyzed oxidants multiple autoimmunity diseases neural network model immune-related biological functions betaine homocysteine methyltransferase privacy choices/manage cookies lupus nephritis based integrated option density dependent remethylation pathway polyunsaturated fatty acid nonapoptotic cell death cell death differ neutrophil-mediated immunity paraffin-embedded glomeruli tissues article/ supplementary material full access cell death dis key enzyme involving ln-related microarray datasets methods data download machine learning

Schema {๐Ÿ—บ๏ธ}

WebPage:
      mainEntity:
         headline:Investigation of ferroptosis-associated molecular subtypes and immunological characteristics in lupus nephritis based on artificial neural network learning
         description:Lupus nephritis (LN) is a severe complication of systemic lupus erythematosus (SLE) with poor treatment outcomes. The role and underlying mechanisms of ferroptosis in LN remain largely unknown. We aimed to explore ferroptosis-related molecular subtypes and assess their prognostic value in LN patients. Molecular subtypes were classified on the basis of differentially expressed ferroptosis-related genes (FRGs) via the Consensus ClusterPlus package. The enriched functions and pathways, immune infiltrating levels, immune scores, and immune checkpoints were compared between the subgroups. A scoring algorithm based on the subtype-specific feature genes identified by artificial neural network machine learning, referred to as the NeuraLN, was established, and its immunological features, clinical value, and predictive value were evaluated in patients with LN. Finally, immunohistochemical analysis was performed to validate the expression and role of feature genes in glomerular tissues from LN patients and controls. A total of 10 differentially expressed FRGs were identified, most of which showed significant correlation. Based on the 10 FRGs, LN patients were classified into two ferroptosis subtypes, which exhibited significant differences in immune cell abundances, immune scores, and immune checkpoint expression. A NeuraLN-related protective model was established based on nine subtype-specific genes, and it exhibited a robustly predictive value in LN. The nomogram and calibration curves demonstrated the clinical benefits of the protective model. The high-NeuraLN group was closely associated with immune activation. Clinical specimens demonstrated the alterations of ALB, BHMT, GAMT, GSTA1, and HAO2 were in accordance with bioinformatics analysis results, GSTA1 and BHMT were negatively correlated with the severity of LN. The classification of ferroptosis subtypes and the establishment of a protective model may form a foundation for the personalized treatment of LN patients.
         datePublished:2024-07-03T00:00:00Z
         dateModified:2024-07-03T00:00:00Z
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         keywords:
            Lupus nephritis
            Ferroptosis
            Molecular subtype
            Immune
            Machine learning
            Protective model
            Rheumatology
            Orthopedics
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                     address:
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ScholarlyArticle:
      headline:Investigation of ferroptosis-associated molecular subtypes and immunological characteristics in lupus nephritis based on artificial neural network learning
      description:Lupus nephritis (LN) is a severe complication of systemic lupus erythematosus (SLE) with poor treatment outcomes. The role and underlying mechanisms of ferroptosis in LN remain largely unknown. We aimed to explore ferroptosis-related molecular subtypes and assess their prognostic value in LN patients. Molecular subtypes were classified on the basis of differentially expressed ferroptosis-related genes (FRGs) via the Consensus ClusterPlus package. The enriched functions and pathways, immune infiltrating levels, immune scores, and immune checkpoints were compared between the subgroups. A scoring algorithm based on the subtype-specific feature genes identified by artificial neural network machine learning, referred to as the NeuraLN, was established, and its immunological features, clinical value, and predictive value were evaluated in patients with LN. Finally, immunohistochemical analysis was performed to validate the expression and role of feature genes in glomerular tissues from LN patients and controls. A total of 10 differentially expressed FRGs were identified, most of which showed significant correlation. Based on the 10 FRGs, LN patients were classified into two ferroptosis subtypes, which exhibited significant differences in immune cell abundances, immune scores, and immune checkpoint expression. A NeuraLN-related protective model was established based on nine subtype-specific genes, and it exhibited a robustly predictive value in LN. The nomogram and calibration curves demonstrated the clinical benefits of the protective model. The high-NeuraLN group was closely associated with immune activation. Clinical specimens demonstrated the alterations of ALB, BHMT, GAMT, GSTA1, and HAO2 were in accordance with bioinformatics analysis results, GSTA1 and BHMT were negatively correlated with the severity of LN. The classification of ferroptosis subtypes and the establishment of a protective model may form a foundation for the personalized treatment of LN patients.
      datePublished:2024-07-03T00:00:00Z
      dateModified:2024-07-03T00:00:00Z
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      pageEnd:16
      license:http://creativecommons.org/publicdomain/zero/1.0/
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         Lupus nephritis
         Ferroptosis
         Molecular subtype
         Immune
         Machine learning
         Protective model
         Rheumatology
         Orthopedics
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                     type:PostalAddress
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                  address:
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                     type:PostalAddress
                  type:Organization
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            name:Juanjuan He
            affiliation:
                  name:Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital
                  address:
                     name:Department of Rheumatology and Immunology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China
                     type:PostalAddress
                  type:Organization
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                     type:PostalAddress
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                     name:Department of Rheumatology and Immunology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China
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               type:PostalAddress
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      name:Jie Tian
      affiliation:
            name:Fujian Provincial Hospital
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               type:PostalAddress
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      name:Zhihan Chen
      affiliation:
            name:Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital
            address:
               name:Department of Rheumatology and Immunology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China
               type:PostalAddress
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      email:[email protected]
      name:Fuyuan Hong
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            name:Fujian Provincial Hospital
            address:
               name:Department of Nephrology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, PR China
               type:PostalAddress
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      email:[email protected]
PostalAddress:
      name:Department of Nephrology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, PR China
      name:Department of Rheumatology and Immunology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China
      name:Department of Nephrology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, PR China
      name:Department of Rheumatology and Immunology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China
      name:Department of Nephrology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, PR China
      name:Department of Rheumatology and Immunology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, China
      name:Department of Nephrology, Shengli Clinical Medical College of Fujian Medical University, Fujian Provincial Hospital, Fuzhou, PR China

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