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pmid:31616474

MUDENG Expression Profiling in Cohorts and Brain Tumor Biospecimens to Evaluate Its Role in Cancer.

Juhyun Shin · Jun-Ha Choi · Seunghwa Jung · Somi Jeong · Jeongheon Oh · Do-Young Yoon · Man Hee Rhee · Jaehong Ahn · Se-Hyuk Kim · Jae-Wook Oh

Frontiers in genetics · 2019 doi:10.3389/fgene.2019.00884

Paper

complete

Experiment

partial

Data

partial

Analysis

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Execution

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Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
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pmid:31616474
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science-record
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https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json
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2026-11-01T15:40:50Z
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2026-11-01T22:00:54Z
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paper object · 10 fields
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title
MUDENG Expression Profiling in Cohorts and Brain Tumor Biospecimens to Evaluate Its Role in Cancer.
doi
10.3389/fgene.2019.00884
pmid
31616474
authors array · 10 items
[0]
Juhyun Shin
[1]
Jun-Ha Choi
[2]
Seunghwa Jung
[3]
Somi Jeong
[4]
Jeongheon Oh
[5]
Do-Young Yoon
[6]
Man Hee Rhee
[7]
Jaehong Ahn
[8]
Se-Hyuk Kim
[9]
Jae-Wook Oh
journal
Frontiers in genetics
year
2019
abstract
Mu-2-related death-inducing gene (MUDENG, MuD) has been reported to be involved in the tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-associated apoptotic pathway of glioblastoma multiforme (GBM) cells; however, its expression level, interactors, and role in tumors are yet to be discovered. To investigate whether MuD expression correlates with cancer progression, we analyzed The Cancer Genome Atlas (TCGA) database using UALCAN and Gene Expression Profiling Interactive Analysis (GEPIA). Differential expression of MuD was detected in 6 and 10 cancer types, respectively. Validation performed using data from the Gene Expression Omnibus database showed that MuD expression is downregulated in KIRC tumor and correlate with higher chance of survival. Upregulation of MuD expression in GBM tumors was detected through GEPIA and high MuD expression correlated with higher survival in proneural GBM, whereas the opposite was observed in classical GBM subtype. GBM biospecimens analysis shows that MuD protein level was upregulated in three of six specimens, whereas mRNA level remained relatively unaltered. Therefore, MuD may exert differential effects according to subtypes, and/or be subjected to post-translational regulation in GBM. Correlation analysis between GBM cohort database and experiments using GBM cell lines revealed its positive effect on regulation of protein phosphatase 2 regulatory subunit B'Epsilon (PPP2R5E) and son of sevenless homolog 2 (SOS2). STRING database analysis indicated that the components of adaptor protein complexes putatively interacted with MuD but showed no correlation in terms of survival of patients with different GBM subtypes. In summary, we analyzed the expression of MuD in publicly available cancer patient data sets, GBM cell lines, and biospecimens to demonstrate its potential role as a biomarker for cancer prognosis and identified its candidate interacting molecules.
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Cox proportional hazard analysis was performed with GBM-BioDP provided at the Glioblastoma Bio Discovery Portal (https://gbm-biodp.nci.nih.gov/) (Celiku et al., 2014).
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sections[4] "Statistical Analysis" paragraph 2
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Cox proportional hazard analysis was performed with GBM-BioDP provided at the Glioblastoma Bio Discovery Portal (https://gbm-biodp.nci.nih.gov/) (Celiku et al., 2014).
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The datasets generated for this study are available on request to the corresponding author.
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sections[18] "Data Availability" paragraph 2
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The datasets generated for this study are available on request to the corresponding author.
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Differential MuD expression and survival correlation revealed by UALCAN and GEPIA.
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Sample Collection From Human Brain Tumors
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Differential MuD expression and survival correlation revealed by UALCAN and GEPIA.
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Clinical characteristics of patients with brain tumor in this study. GB, glioblastoma; ODG, oligodendroglioma; ED, ependymoma.
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Expression Analysis Revealed Putative Post-Translational Regulation of MuD
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Clinical characteristics of patients with brain tumor in this study. GB, glioblastoma; ODG, oligodendroglioma; ED, ependymoma.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31616474", "kind": "science-record", "revision": 7, "content_hash": "sha256:4a9d7bfdaa9c1acc7d653309d945c9bbc47414f27d8a1d6f2c0eeb80a6696906", "created_at": "2026-11-01T15:40:50Z", "updated_at": "2026-11-01T22:00:54Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "MUDENG Expression Profiling in Cohorts and Brain Tumor Biospecimens to Evaluate Its Role in Cancer.", "doi": "10.3389/fgene.2019.00884", "pmid": "31616474", "authors": ["Juhyun Shin", "Jun-Ha Choi", "Seunghwa Jung", "Somi Jeong", "Jeongheon Oh", "Do-Young Yoon", "Man Hee Rhee", "Jaehong Ahn", "Se-Hyuk Kim", "Jae-Wook Oh"], "journal": "Frontiers in genetics", "year": 2019, "abstract": "Mu-2-related death-inducing gene (MUDENG, MuD) has been reported to be involved in the tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-associated apoptotic pathway of glioblastoma multiforme (GBM) cells; however, its expression level, interactors, and role in tumors are yet to be discovered. To investigate whether MuD expression correlates with cancer progression, we analyzed The Cancer Genome Atlas (TCGA) database using UALCAN and Gene Expression Profiling Interactive Analysis (GEPIA). Differential expression of MuD was detected in 6 and 10 cancer types, respectively. Validation performed using data from the Gene Expression Omnibus database showed that MuD expression is downregulated in KIRC tumor and correlate with higher chance of survival. Upregulation of MuD expression in GBM tumors was detected through GEPIA and high MuD expression correlated with higher survival in proneural GBM, whereas the opposite was observed in classical GBM subtype. GBM biospecimens analysis shows that MuD protein level was upregulated in three of six specimens, whereas mRNA level remained relatively unaltered. Therefore, MuD may exert differential effects according to subtypes, and/or be subjected to post-translational regulation in GBM. Correlation analysis between GBM cohort database and experiments using GBM cell lines revealed its positive effect on regulation of protein phosphatase 2 regulatory subunit B'Epsilon (PPP2R5E) and son of sevenless homolog 2 (SOS2). STRING database analysis indicated that the components of adaptor protein complexes putatively interacted with MuD but showed no correlation in terms of survival of patients with different GBM subtypes. 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