Evidence map›Paper›PMID 11853549›Full record

ArticleThe Biochemical journal2002

Transcriptional regulation of the human manganese superoxide dismutase gene: the role of specificity protein 1 (Sp1) and activating protein-2 (AP-2).

Yong Xu, Sureerut Porntadavity, Daret K St Clair

Open access · bronzeAbstract read
In one paragraph

Article in The Biochemical journal, 2002. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

56 citing papers in PubMed, 123 citations in OpenAlex.

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  14. Insights into the Dichotomous Regulation of SOD2 in Cancer.Antioxidants (Basel, Switzerland) · 2017
    Review
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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

3 authors at 1 institution in 1 country.

Yong XuGraduate Center for Toxicology, University of Kentucky, 361 Health Sciences Research Building, Lexington KY 40536, USA.
Sureerut Porntadavity
Daret K St Clair
Mahidol University · TH

Funding

REDOX REGULATION OF TUMOR SUPPRESSION BY MNSODR01CA073599 · NCI · UNIVERSITY OF KENTUCKY · PI ST CLAIR, DARET K · 1998 to 2012
$4.0M
Mechansins of MnSOD expression in normal and tumor cellsR01CA049797 · NCI · UNIVERSITY OF KENTUCKY · PI ST CLAIR, DARET K · 1996 to 2014
$3.3M
MNSOD AND DRUG RESISTANCE AND CARDIAC TOXICITYR01CA059835 · NCI · UNIVERSITY OF KENTUCKY · PI ST CLAIR, DARET K · 1995 to 1999
–
MECHANISM OF MNSOD EXPRESSION IN NORMAL &TUMOR CELLSR29CA049797 · NCI · WAKE FOREST UNIVERSITY · PI ST CLAIR, DARET K · 1990 to 1994
–
NCI NIH HHS CA 49797NCI NIH HHS CA 59835NCI NIH HHS CA 73599NHLBI NIH HHS HL 03544
6 · The paper itself

Abstract

Manganese superoxide dismutase (MnSOD) plays an important role in regulating cellular redox conditions. Expression of MnSOD has been shown to protect against damage by oxidative stress and to suppress the malignant phenotype of human cancer cells. We have previously cloned the human MnSOD (SOD2) gene and analysed its 5' proximal promoter, which has been characterized by a lack of a TATA or CAAT box and the presence of multiple GC boxes. To define further the molecular mechanisms for the regulation of MnSOD expression, multiple transcription factor-binding motifs containing overlapping specificity protein 1 (Sp1)- and activator protein (AP)-2-binding sites were identified by DNase I footprinting analysis. Functional studies in three cell lines with different levels of Sp1 and AP-2 proteins suggested that the cellular levels of these proteins may differentially regulate transcription via GC-binding motifs in the human SOD2 promoter. Co-transfection of an Sp1 expression vector resulted in an increase in the transcription of the promoter-driven reporter gene. In contrast, co-transfection of the AP-2 expression vector caused a decrease in transcription. Direct mutagenesis analysis of Sp1- and AP-2-binding sites showed that Sp1 is essential for transcription of the human SOD2 gene, whereas AP-2 plays a negative role in the transcription. Immunoprecipitation of Sp1 and AP-2 proteins demonstrated that Sp1 interacts with AP-2 in vivo. Two-hybrid analysis revealed that interaction between Sp1 and AP-2 plays both a positive and negative role in the transcription of the reporter gene in vivo. Taken together, our data indicate that AP-2 down-regulates transcription of the human SOD2 gene via its interaction with Sp1 within the promoter region. These findings, coupled with our previous observation that several cancer cell lines have mutations in the promoter region of the human MnSOD gene, which lead to an increase in an AP-2-binding site and a decrease in the promoter activity, signal the importance of understanding the promoter structure and the regulation of the human SOD2 gene by Sp1 and AP-2.

Indexed as

Gene Expression Regulation, EnzymologicTranscription, GeneticBase SequenceBinding SitesCarcinoma, HepatocellularCell Line, TransformedCloning, MolecularCytosineDNA-Binding ProteinsDNA PrimersGenes, ReporterGuanineHeLa CellsHumansKruppel-Like Transcription FactorsLiver NeoplasmsCytosineDNA-Binding ProteinsDNA PrimersGuanineKLF12 protein, humanKruppel-Like Transcription FactorsRecombinant ProteinsSuperoxide DismutaseTranscription Factor AP-2Transcription Factors

Identifiers

PMID11853549
PMCPMC1222401
OpenAlexW2092659658

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.