TRIM8-associated non-coding RNA panel as a biomarker for Lupus nephritis activity

Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs ( lnc-SSBP2-1:1 and hsa-miR-126-5p ) as potential non-invasive biomarkers for LN activity. Methods Bioi...

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Published in:Journal of translational medicine Vol. 23; no. 1; pp. 1229 - 10
Main Authors: Elgawad, Mostafa Abdelnasier Abd, Shinnawy, Howayda Abdelhamid El, Eissa, Sanaa, Ali, Nouran Abdelfattah Sayed, Behairy, Maha Abdelmoneim, Kamel, Cherry Reda, Kamel, Marwa Mostafa
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Abstract Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs ( lnc-SSBP2-1:1 and hsa-miR-126-5p ) as potential non-invasive biomarkers for LN activity. Methods Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1 and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR. Results TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN ( p  < 0.001), while hsa-miR-126-5p was reduced ( p  < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1 , and negatively with hsa-miR-126-5p . Conclusions This study highlights TRIM8 -associated ncRNA regulatory network as promising biomarkers in LN activωity, with potential clinical impact. Graphical abstract Highlights TRIM8 and lnc-SSBP2-1:1 are upregulated, hsa-miR-126-5p is downregulated in active LN Biomarkers strongly correlated with SLEDAI-2K disease activity scores High diagnostic accuracy (AUCs > 0.93) in distinguishing active vs inactive LN Potential non-invasive tool to complement current LN monitoring
AbstractList Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs (lnc-SSBP2-1:1 and hsa-miR-126-5p) as potential non-invasive biomarkers for LN activity.BACKGROUNDLupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs (lnc-SSBP2-1:1 and hsa-miR-126-5p) as potential non-invasive biomarkers for LN activity.Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR.METHODSBioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR.TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN (p < 0.001), while hsa-miR-126-5p was reduced (p < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1, and negatively with hsa-miR-126-5p.RESULTSTRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN (p < 0.001), while hsa-miR-126-5p was reduced (p < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1, and negatively with hsa-miR-126-5p.This study highlights TRIM8-associated ncRNA regulatory network as promising biomarkers in LN activωity, with potential clinical impact.CONCLUSIONSThis study highlights TRIM8-associated ncRNA regulatory network as promising biomarkers in LN activωity, with potential clinical impact.
Abstract Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs (lnc-SSBP2-1:1 and hsa-miR-126-5p) as potential non-invasive biomarkers for LN activity. Methods Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR. Results TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN (p < 0.001), while hsa-miR-126-5p was reduced (p < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1, and negatively with hsa-miR-126-5p. Conclusions This study highlights TRIM8-associated ncRNA regulatory network as promising biomarkers in LN activωity, with potential clinical impact. Graphical abstract
Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs (lnc-SSBP2-1:1 and hsa-miR-126-5p) as potential non-invasive biomarkers for LN activity. Methods Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR. Results TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN (p < 0.001), while hsa-miR-126-5p was reduced (p < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1, and negatively with hsa-miR-126-5p. Conclusions This study highlights TRIM8-associated ncRNA regulatory network as promising biomarkers in LN activ[omega]ity, with potential clinical impact. Graphical abstract Keywords: Lupus nephritis, TRIM8, hsa-miR-126-5p, lnc-SSBP2-1:1, non-coding RNA network, Biomarkers, Disease activity
Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs (lnc-SSBP2-1:1 and hsa-miR-126-5p) as potential non-invasive biomarkers for LN activity. Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR. TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN (p < 0.001), while hsa-miR-126-5p was reduced (p < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1, and negatively with hsa-miR-126-5p. This study highlights TRIM8-associated ncRNA regulatory network as promising biomarkers in LN activ[omega]ity, with potential clinical impact.
Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs (lnc-SSBP2-1:1 and hsa-miR-126-5p) as potential non-invasive biomarkers for LN activity. Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR. TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN (p < 0.001), while hsa-miR-126-5p was reduced (p < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1, and negatively with hsa-miR-126-5p. This study highlights TRIM8-associated ncRNA regulatory network as promising biomarkers in LN activωity, with potential clinical impact.
Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its associated non-coding RNAs ( lnc-SSBP2-1:1 and hsa-miR-126-5p ) as potential non-invasive biomarkers for LN activity. Methods Bioinformatics analyses were initially employed to identify candidate mRNA and associated non-coding RNAs (ncRNAs) implicated in LN. Expression profiles of TRIM8lnc-SSBP2-1:1 and hsa-miR-126-5p were validated in blood samples from 40 active LN, 30 inactive LN patients, and 20 healthy individuals via real-time PCR. Results TRIM8 mRNA and lnc-SSBP2-1:1 lncRNA levels were notably upregulated in active LN ( p  < 0.001), while hsa-miR-126-5p was reduced ( p  < 0.001). SLEDAI-2K scores correlated positively with TRIM8 mRNA and lnc-SSBP2-1:1 , and negatively with hsa-miR-126-5p . Conclusions This study highlights TRIM8 -associated ncRNA regulatory network as promising biomarkers in LN activωity, with potential clinical impact. Graphical abstract Highlights TRIM8 and lnc-SSBP2-1:1 are upregulated, hsa-miR-126-5p is downregulated in active LN Biomarkers strongly correlated with SLEDAI-2K disease activity scores High diagnostic accuracy (AUCs > 0.93) in distinguishing active vs inactive LN Potential non-invasive tool to complement current LN monitoring
ArticleNumber 1229
Audience Academic
Author Kamel, Marwa Mostafa
Eissa, Sanaa
Kamel, Cherry Reda
Shinnawy, Howayda Abdelhamid El
Ali, Nouran Abdelfattah Sayed
Elgawad, Mostafa Abdelnasier Abd
Behairy, Maha Abdelmoneim
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Issue 1
Keywords Biomarkers
Disease activity
Lupus nephritis
non-coding RNA network
TRIM8
hsa-miR-126-5p
lnc-SSBP2-1:1
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Snippet Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8...
Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8 gene and its...
Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the TRIM8...
Abstract Background Lupus nephritis (LN) represents a major complication in systemic lupus erythematosus (SLE). The objective of this study was to evaluate the...
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SubjectTerms Adult
Analysis
B cells
Biological markers
Biomarkers
Biomarkers - blood
Biomarkers - metabolism
Biomedical and Life Sciences
Biomedicine
Care and treatment
Carrier Proteins - genetics
Carrier Proteins - metabolism
Case-Control Studies
Complications and side effects
Development and progression
Diagnosis
Ethylenediaminetetraacetic acid
Female
hsa-miR-126-5p
Humans
Immune response
Immunobiology and immunotherapy
lnc-SSBP2-1:1
Lupus
Lupus nephritis
Lupus Nephritis - blood
Lupus Nephritis - genetics
Male
Medicine/Public Health
MicroRNAs - genetics
MicroRNAs - metabolism
Middle Aged
Nephritis
Nerve Tissue Proteins
non-coding RNA network
Polymerase chain reaction
Risk factors
RNA
RNA, Long Noncoding - genetics
RNA, Messenger - genetics
RNA, Messenger - metabolism
RNA, Untranslated - genetics
RNA, Untranslated - metabolism
Systemic lupus erythematosus
Testing
TRIM8
Tripartite Motif Proteins
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Title TRIM8-associated non-coding RNA panel as a biomarker for Lupus nephritis activity
URI https://link.springer.com/article/10.1186/s12967-025-07137-3
https://www.ncbi.nlm.nih.gov/pubmed/41194165
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