Evidence map›Paper›PMID 23938323›Full record

ArticleThe American journal of pathology2013

Cooperation between Dmp1 loss and cyclin D1 overexpression in breast cancer.

Sinan Zhu, Ryan T Mott, Elizabeth A Fry, Pankaj Taneja, George Kulik, Guangchao Sui, Kazushi Inoue

Open access · hybridAbstract read
In one paragraph

Article in The American journal of pathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Survival of Lung Cancer Patients Dependent on the LOH Status forInternational journal of molecular sciences · 2020
    Article
  7. Article
  8. The double dealing of cyclin D1.Cell cycle (Georgetown, Tex.) · 2020
    Review
  9. Article
  10. Article
  11. c-MYB and DMTF1 in Cancer.Cancer investigation · 2019
    Review
  12. Translocations involving ETS family proteins in human cancer.Integrative cancer science and therapeutics · 2018
    Article
  13. Aberrant expression of p16Cancer reports and reviews · 2018
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  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

7 authors at 2 institutions in 2 countries.

Sinan ZhuDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, North Carolina; Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina; Graduate Program in Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Ryan T MottDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Elizabeth A FryDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Pankaj TanejaDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, North Carolina; Department of Biotechnology, Radiation Biosciences, Institute of Nuclear Medicine and Allied Science, SK Majumdar Road, Delhi, India.
George KulikDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Guangchao SuiDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina. Electronic address: gsui@wakehealth.edu.
Kazushi InoueDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, North Carolina; Department of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina; Graduate Program in Molecular Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina. Electronic address: kinoue2@triad.rr.com.
Wake Forest University · USInstitute of Nuclear Medicine & Allied Sciences · IN

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
Stress-activated signaling in prostate cancerR01CA118329 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI KULIK, GEORGE A · 2008 to 2012
$2.5M
NCI NIH HHS 5R01CA106314NCI NIH HHS P30 CA012197NCI NIH HHS R01 CA106314NCI NIH HHS R01 CA118329NCI NIH HHS R01CA118329
6 · The paper itself

Abstract

Cyclin D1 is a component of the core cell-cycle machinery and is frequently overexpressed in breast cancer. It physically interacts with the tumor suppressor Dmp1 that attenuates the oncogenic signals from Ras and HER2 by inducing Arf/p53-dependent cell-cycle arrest. Currently, the biological significance of Dmp1-cyclin D1 interplay in breast cancer has not been determined. Here, we show that cyclin D1 bound to Dmp1 to activate both Arf and Ink4a promoters and, consequently, induced apoptosis or G2/M cell-cycle delay in normal cells to protect them from neoplastic transformation. The cyclin D1-induced Ink4a/Arf gene expression was dependent on Dmp1 because the induction was not detected in Dmp1-deficient or DMP1-depleted cells. Arf/Ink4a expression was increased in pre-malignant mammary glands from Dmp1(+/+);MMTV-cyclin D1 and Dmp1(+/+);MMTV-D1T286A mice but significantly down-regulated in those from Dmp1-deficient mice. Selective Dmp1 deletion was found in 21% of the MMTV-D1 and D1T286A mammary carcinomas, and the Dmp1 heterozygous status significantly accelerated mouse mammary tumorigenesis with reduced apoptosis and increased metastasis. Overall, our study reveals a pivotal role of combined Dmp1 loss and cyclin D1 overexpression in breast cancer.

Indexed as

AnimalsApoptosisBreast NeoplasmsCarcinogenesisCyclin D1Cyclin-Dependent Kinase Inhibitor p16FemaleFibroblastsG2 PhaseGene Expression Regulation, NeoplasticHumansMammary Neoplasms, ExperimentalMammary Tumor Virus, MouseMiceMice, TransgenicMitosisCdkn2a protein, mouseCyclin D1Cyclin-Dependent Kinase Inhibitor p16DMTF1 protein, humanDmtf1 protein, mouseTranscription Factors

Identifiers

PMID23938323
PMCPMC3791682
OpenAlexW2138177440

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.