Evidence map›Paper›PMID 27553713›Full record

ReviewInternational journal of cancer2017

Oncogenic and tumor-suppressive mouse models for breast cancer engaging HER2/neu.

Elizabeth A Fry, Pankaj Taneja, Kazushi Inoue

Open access · bronzeAbstract readReview
In one paragraph

Review in International journal of cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

26 citing papers in PubMed, 38 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Survival of Lung Cancer Patients Dependent on the LOH Status forInternational journal of molecular sciences · 2020
    Article
  10. Article
  11. Review
  12. Past, Present, and Future of Anticancer Nanomedicine.International journal of nanomedicine · 2020
    Review
  13. Article
  14. Article
  15. Article
  16. c-MYB and DMTF1 in Cancer.Cancer investigation · 2019
    Review
  17. Review
  18. Translocations involving ETS family proteins in human cancer.Integrative cancer science and therapeutics · 2018
    Article
  19. Article
  20. Aberrant expression of p16Cancer reports and reviews · 2018
    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

3 authors at 2 institutions in 2 countries.

Elizabeth A FryThe Department of Pathology, Wake Forest University Health Sciences, Medical Center Boulevard, Winston-Salem, NC.
Pankaj TanejaDepartment of Biotechnology, Sharda University, Greater Noida, Uttar Pradesh, India.
Kazushi InoueThe Department of Pathology, Wake Forest University Health Sciences, Medical Center Boulevard, Winston-Salem, NC.
Wake Forest University · USSharda University · IN

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 R01 CA106314
6 · The paper itself

Abstract

The human c-ErbB2 (HER2) gene is amplified in ∼20% of human breast cancers (BCs), but the protein is overexpressed in ∼30% of the cases indicating that multiple different mechanisms contribute to HER2 overexpression in tumors. It has long been used as a molecular marker of BC for subcategorization for the prediction of prognosis and determination of therapeutic strategies. In comparison to ER(+) BCs, HER2-positive BCs are more invasive, but the patients respond to monoclonal antibody therapy with trastuzumab or tyrosine kinase inhibitors at least at early stages. To understand the pathophysiology of HER2-driven carcinogenesis and test HER2-targeting therapeutic agents in vivo, numerous mouse models have been created that faithfully reproduce HER2(+) BCs in mice. They include MMTV-neu (active mutant or wild type, rat neu or HER2) models, neu promoter-driven neuNT-transgenic mice, neuNT-knock-in mice at the neu locus and doxycycline-inducible neuNT-transgenic models. HER2/neu activates the Phosphatidylinositol-3 kinase-AKT-NF-κB pathway to stimulate the mitogenic cyclin D1/Cdk4-Rb-E2F pathway. Of note, overexpression of HER2 also stimulates the cell autonomous Dmp1-Arf-p53 tumor suppressor pathway to quench oncogenic signals to prevent the emergence of cancer cells. Hence tumor development by MMTV-neu mice was dramatically accelerated in mice that lack Dmp1, Arf or p53 with invasion and metastasis. Expressions of neuNT under the endogenous promoter underwent gene amplification, closely recapitulating human HER2(+) BCs. MMTV-HER2 models have been shown to be useful to test humanized monoclonal antibodies to HER2. These mouse models will be useful for the screening of novel therapeutic agents against BCs with HER2 overexpression.

Indexed as

AnimalsBreast NeoplasmsCarcinogenesisDisease Models, AnimalErb-b2 Receptor Tyrosine KinasesHumansMiceMice, TransgenicOncogenesTumor Suppressor ProteinsErb-b2 Receptor Tyrosine KinasesTumor Suppressor Proteinsbreast cancerdisease modelDmp1Dmtf1HER2/neup53PI3Kpreventiontarget therapytransgenic mice

Identifiers

PMID27553713
PMCPMC5159240
OpenAlexW2508171651

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.