Evidence map›Paper›PMID 21062982›Full record

ArticleCancer research2010

Critical roles of DMP1 in human epidermal growth factor receptor 2/neu-Arf-p53 signaling and breast cancer development.

Pankaj Taneja, Dejan Maglic, Fumitake Kai, Takayuki Sugiyama, Robert D Kendig, Donna P Frazier, Mark C Willingham, Kazushi Inoue

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

32 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Identification of DMP1 as Novel p53 Repressed Transcriptional Target.International journal of molecular sciences · 2026
    Article
  3. Article
  4. Article
  5. Survival of Lung Cancer Patients Dependent on the LOH Status forInternational journal of molecular sciences · 2020
    Article
  6. Article
  7. Article
  8. c-MYB and DMTF1 in Cancer.Cancer investigation · 2019
    Review
  9. Aberrant expression of p16Cancer reports and reviews · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Transcription factors that interact with p53 and Mdm2.International journal of cancer · 2016
    Review
  16. Clinical applications of mouse models for breast cancer engaging HER2/neu.Integrative cancer science and therapeutics · 2016
    Article
  17. Novel Molecular Markers for Breast Cancer.Biomarkers in cancer · 2016
    Review
  18. Article
  19. Aberrant expression of cyclin D1 in cancer.Signal transduction insights · 2015
    Article
  20. Review
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 1 institution in 1 country.

Pankaj TanejaDepartments of Pathology and Cancer Biology and Graduate Program in Molecular Medicine, Wake Forest University Health Sciences, Medical Center Boulevard, Winston-Salem, North Carolina.
Dejan Maglic
Fumitake Kai
Takayuki Sugiyama
Robert D Kendig
Donna P Frazier
Mark C Willingham
Kazushi Inoue
Wake Forest University · US

Funding

Roles of DMP1 in Ras signaling and lung cancerR01CA106314 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUI, GUANGCHAO · 2004 to 2013
$2.6M
NCI NIH HHS 2R01CA106314NCI NIH HHS R01 CA106314
6 · The paper itself

Abstract

Human epidermal growth factor receptor 2 (HER2) overexpression stimulates cell growth in p53-mutated cells while it inhibits cell proliferation in those with wild-type p53, but the molecular mechanism is unknown. The Dmp1 promoter was activated by HER2/neu through the phosphatidylinositol-3'-kinase-Akt-NF-κB pathway, which in turn stimulated Arf transcription. Binding of p65 and p52 subunits of NF-κB was shown to the Dmp1 promoter and that of Dmp1 to the Arf promoter on HER2/neu overexpression. Both Dmp1 and p53 were induced in premalignant lesions from mouse mammary tumor virus-neu mice, and mammary tumorigenesis was significantly accelerated in both Dmp1+/- and Dmp1-/- mice. Selective deletion of Dmp1 and/or overexpression of Tbx2/Pokemon was found in >50% of wild-type HER2/neu carcinomas, although the involvement of Arf, Mdm2, or p53 was rare. Tumors from Dmp1+/-, Dmp1-/-, and wild-type neu mice with hemizygous Dmp1 deletion showed significant downregulation of Arf and p21Cip1/WAF1, showing p53 inactivity and more aggressive phenotypes than tumors without Dmp1 deletion. Notably, endogenous hDMP1 mRNA decreased when HER2 was depleted in human breast cancer cells. Our study shows the pivotal roles of Dmp1 in HER2/neu-p53 signaling and breast carcinogenesis.

Indexed as

Signal TransductionAnimalsBase SequenceBlotting, WesternBreast NeoplasmsCell Line, TumorCells, CulturedCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21Epithelial CellsErb-b2 Receptor Tyrosine KinasesExtracellular Matrix ProteinsFemaleGene ExpressionHumansMaleCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21DMP1 protein, humanErb-b2 Receptor Tyrosine KinasesExtracellular Matrix ProteinsPhosphoproteinsTumor Suppressor Protein p53

Identifiers

PMID21062982
PMCPMC3073839
OpenAlexW2121792822

What OpenQuestion holds

Textmetadata
LicenceTDM
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.