Evidence map›Paper›PMID 12716893›Full record

ArticleThe Journal of biological chemistry2003

Chromium(VI) down-regulates heavy metal-induced metallothionein gene transcription by modifying transactivation potential of the key transcription factor, metal-responsive transcription factor 1.

Sarmila Majumder, Kalpana Ghoshal, Dennis Summers, Shoumei Bai, Jharna Datta, Samson T Jacob

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
  2. Mixture toxicity of the combinations of silver nanoparticles and environmental pollutants.Environmental science and pollution research international · 2020
    Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Repression of miR-143 mediates Cr (VI)-induced tumor angiogenesis via IGF-IR/IRS1/ERK/IL-8 pathway.Toxicological sciences : an official journal of the Society of Toxicology · 2013
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Methylation and silencing of protein tyrosine phosphatase receptor type O in chronic lymphocytic leukemia.Clinical cancer research : an official journal of the American Association for Cancer Research · 2007
    Article
  19. Article
  20. Article
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

6 authors at 1 institution in 1 country.

Sarmila MajumderDepartment of Molecular and Cellular Biochemistry, The Ohio State University, College of Medicine, The Ohio State University, Columbus, Ohio 43210, USA.
Kalpana Ghoshal
Dennis Summers
Shoumei Bai
Jharna Datta
Samson T Jacob
The Ohio State University · US

Funding

DNA METHYLATION AND GENE EXPRESSION IN CANCER CELLSR01ES010874 · NIEHS · OHIO STATE UNIVERSITY · PI JACOB, SAMSON T · 2000 to 2004
$1.6M
MOLECULAR MECHANISMS OF METALLOTHIONEIN INDUCTIONR01CA081024 · NCI · OHIO STATE UNIVERSITY · PI JACOB, SAMSON T · 2000 to 2003
$1.2M
NCI NIH HHS CA81024NCI NIH HHS R01 CA081024NIEHS NIH HHS ES10874NIEHS NIH HHS R01 ES010874
6 · The paper itself

Abstract

The robust induction of metallothionein-I and II (MT-I and MT-II) genes by several heavy metals such as zinc and cadmium requires the specific transcription factor metal-responsive transcription factor 1 (MTF1). Chromium (VI), a major environmental carcinogen, not only failed to activate these genes but also inhibited their induction by Zn2+ or Cd2+. The heavy metal-induced expression of another MTF1 target gene, zinc transporter 1 (ZnT-1), was also down-regulated by Cr6+. By contrast, the expression of two MTF1-independent Cd2+-inducible genes, heme oxygenase 1 (HO-1) and HSP-70, was not sensitive to Cr6+. Cr6+ did not also affect the expression of housekeeping genes such as GAPDH or beta-actin. Stable cell lines overexpressing variable levels of MTF1, the key transactivator of the MT genes, demonstrated differential resistance toward the inhibitory effect of Cr6+, indicating MTF1 as a target of chromium toxicity. The basal and inducible binding of MTF1 to metal response elements was not affected by treatment of cells with Cr6+. Transient transfection studies showed that the ability of MTF1 to transactivate the MT-I promoter was significantly compromised by Cr6+. The fusion protein consisting of a Gal-4 DNA binding domain and one or more of the three transactivation domains of MTF1, namely the acidic domain, proline-rich domain, and serine-threonine rich domain, activated the GAL-4-driven luciferase gene to different degrees, but all were sensitive to Cr6+. MTF1 null cells were prone to apoptosis after exposure to Zn2+ or Cd2+ that was augmented in presence Cr6+, whereas the onset of apoptosis was significantly delayed in cells overexpressing MTF1.

Indexed as

Down-RegulationTranscriptional ActivationTranscription, GeneticAnnexin A5ApoptosisBlotting, NorthernBlotting, WesternCell LineChromiumColoring AgentsDNA-Binding ProteinsDNA FootprintingHeme Oxygenase-1Heme Oxygenase (Decyclizing)HSP70 Heat-Shock ProteinsHumansAnnexin A5ChromiumColoring AgentsDNA-Binding ProteinsHeme Oxygenase-1Heme Oxygenase (Decyclizing)HMOX1 protein, humanHSP70 Heat-Shock ProteinsMembrane ProteinsMetallothioneinMetals, HeavyRecombinant Fusion ProteinsTetrazolium SaltsThiazolesthiazolyl blueTranscription Factor MTF-1Transcription FactorsZinc

Identifiers

PMID12716893
PMCPMC2365495
OpenAlexW2076917025

What OpenQuestion 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 OpenQuestion graph.