Evidence map›Paper›PMID 16878159›Full record

ArticleOncogene2006

Expression of Dmp1 in specific differentiated, nonproliferating cells and its regulation by E2Fs.

A Mallakin, P Taneja, L A Matise, M C Willingham, K Inoue

Open access · greenAbstract read
In one paragraph

Article in Oncogene, 2006. 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
1.2field-weighted citation impact, top 22% 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, 34 citations in OpenAlex.

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

5 authors at 1 institution in 1 country.

A MallakinDepartment of Pathology, Wake Forest University Health Sciences, Medical Center Boulevard, Winston-Salem, NC 27157-0001, USA.
P Taneja
L A Matise
M C Willingham
K Inoue
Wake Forest University · US

Funding

Tumor Tissue CoreP30CA012197 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Ruben A. Mesa · 1985 to 2026
$55.4M
Roles of DMP1 in Ras signaling and lung cancerR01CA106314 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUI, GUANGCHAO · 2004 to 2013
$2.6M
Cellular Responses to Cancer Drug-Induced Genomic BreaksR01CA106312 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI BEERMAN, TERRY A · 2005 to 2008
$1.1M
NCI NIH HHS 5R01CA106312-02NCI NIH HHS CA12197-31NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA106314
6 · The paper itself

Abstract

Dmp1 is a Myb-like transcription factor that transmits oncogenic Ras-Raf signaling to the Arf-p53 pathway and induces cell cycle arrest. Immunohistochemical staining was performed to identify the pattern of Dmp1 expression in normal murine tissues compared with the proliferation marker, Ki67. In thymus, the nuclei of mature T lymphocytes in the medulla were strongly positive for Dmp1, whereas Ki67 was detected only in the cortex. In intestine, Dmp1 was detected in the nuclei of superficial layers of the villi, whereas Ki67-positive cells were confined to the lower one-third of the crypt. Double staining for Dmp1 and Ki67 revealed that these two proteins were expressed in mutually exclusive fashion in nearly all the tissues examined. Subsets of E2Fs were specifically bound to the Dmp1 promoter upon mitogenic signaling and E2Fs 1-4 inhibited the Dmp1 promoter in a reporter assay. The Dmp1 promoter was repressed when the cells entered the S to G2/M phase of the cell cycle when both Dmp1 and Arf expressions were downregulated. The Dmp1 mRNA was not downregulated by serum in E2F-DB(+) cells, suggesting that the Dmp1 promoter repression is E2F-dependent. This explains why the Dmp1 and Ki67-positive cells are stained in mutually exclusive fashion in normal tissues.

Indexed as

3T3 CellsAnimalsBase SequenceBlotting, WesternE2F Transcription FactorsImmunohistochemistryKi-67 AntigenMiceMolecular Sequence DataPromoter Regions, GeneticRNA, MessengerTranscription FactorsDmtf1 protein, mouseE2F Transcription FactorsKi-67 AntigenRNA, MessengerTranscription Factors

Identifiers

PMID16878159
PMCPMC2077854
OpenAlexW1973677548

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.