Evidence map›Paper›PMID 32594352›Full record

ArticleMolecular neurobiology2020

Nuclear Respiratory Factor 1 (NRF1) Transcriptional Activity-Driven Gene Signature Association with Severity of Astrocytoma and Poor Prognosis of Glioblastoma.

Kaumudi Bhawe, Quentin Felty, Changwon Yoo, Nasreen Z Ehtesham, Seyed E Hasnain, Varindera Paul Singh, Ishani Mohapatra, Deodutta Roy

Abstract read
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In one paragraph

Article in Molecular neurobiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 47 citations in OpenAlex.

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  2. Archives of medical science : AMS · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Kaumudi BhaweDepartment of Environmental Health Sciences, Florida International University, Miami, FL, 33199, USA.
Quentin FeltyDepartment of Environmental Health Sciences, Florida International University, Miami, FL, 33199, USA.
Changwon YooDepartment of Biostatistics, Florida International University, Miami, FL, 33199, USA.
Nasreen Z EhteshamNational Institute of Pathology, Safdarjung Hospital Campus, New Delhi, India.
Seyed E HasnainJH Institute of Molecular Medicine, Jamia Hamdard, New Delhi, India.
Varindera Paul SinghInstitute of Neuroscience, Medanta-The Medicity, Gurugram, India.
Ishani MohapatraInstitute of Neuroscience, Medanta-The Medicity, Gurugram, India.
Deodutta RoyDepartment of Environmental Health Sciences, Florida International University, Miami, FL, 33199, USA. droy@fiu.edu.ORCID http://orcid.org/0000-0001-6409-1341
Florida International University · USMedanta The Medicity · INJamia Hamdard · INSafdarjang Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite tremendous progress in understanding the pathobiology of astrocytoma, major gaps remain in our knowledge of the molecular basis underlying the aggressiveness of high-grade astrocytoma (glioblastoma - GBM). Recently, we and others have shown nuclear respiratory factor 1 (NRF1) transcription factor being highly active in human cancers, but its role in astrocytoma remains unknown. Therefore, the purpose of this study was to uncover the role of NRF1 in the progression of GBM. NRF1 has higher mRNA expression and transcription factor activity in astrocytoma compared to non-tumor brain tissue. NRF1 activity also correlated with the aggressiveness of cancer. Increased NRF1 TF activity coupled with overexpression of RHOG was associated with poor survival of GBM patients. NRF1 activity was associated with transcriptomic signatures of neurogenesis, cell stemness, epithelial-mesenchymal transition and cell cycle progression. Overexpression of CDK4, AKT1, APAF1, HDAC1, NBN, TGFB1, & TNFRSF1A and downregulation of CASP3, IL7, STXBP1 and OPA1 predicted GBM malignancy in high expressors of NRF1 activity. Increased expression of the NRF1 motif containing genes, H6PD, NAT10, NBEAL2, and RNF19B predicted poor survival of IDH1 wild-type GBM patients. Poor survival outcomes and resistance to Temozolomide therapy were associated with higher NRF1 expression including its targets - LDHA, ZMAT3, NSUN2, ARMC5, NDEL1, CLPTM1L, ALKBH5, YIPF5, PPP2CA, and TFG. These findings suggest that aberrant NRF1 activity may contribute to the pathogenesis of GBM and severity of astrocytoma. Further analyses of NRF1 gene signatures will pave the way for next generation targeted therapies and drug combination strategies for GBM patients.

Indexed as

Gene Expression ProfilingSeverity of Illness IndexTranscription, GeneticAdultApoptosisAstrocytomaBiomarkers, TumorBrain NeoplasmsCell CycleCell DifferentiationCohort StudiesCyclin-Dependent Kinase 4Drug Resistance, NeoplasmEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticBiomarkers, TumorCyclin-Dependent Kinase 4Nerve Tissue ProteinsNuclear Respiratory Factor 1RNA, MessengerTemozolomideCancer stem cellsCDK4EMTGlioblastomaNRF1 activityRHOG

Identifiers

PMID32594352
OpenAlexW3037540475

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.