Evidence map›Paper›PMID 19450579›Full record

ReviewExperimental and molecular pathology2009

The role of HER2 in early breast cancer metastasis and the origins of resistance to HER2-targeted therapies.

Jaclyn A Freudenberg, Qiang Wang, Makoto Katsumata, Jeffrey Drebin, Izumi Nagatomo, Mark I Greene

Registry-linked trialAbstract readReview
In one paragraph

Review in Experimental and molecular pathology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05030519 (A Study of Diarrhea and Intestinal Flora Changes Caused by Pyrotinib in Breast Cancer), which is not on this map. Cited by 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
4.3field-weighted citation impact, top 5% 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.

NCT05030519 unknown statusnot on this mapstarted 2021, after this paper: background citation

A Study of Diarrhea and Intestinal Flora Changes Caused by Pyrotinib in Breast Cancer

TypeobservationalSponsorZhejiang Cancer HospitalRan2021 to 2022Enrolled50ConditionsBreast CancerArmsPyrotinib
3 · Its place in the literature

Who cites it

60 citing papers in PubMed, 124 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Th1 cytokine interferon gamma improves response in HER2 breast cancer by modulating the ubiquitin proteasomal pathway.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
  18. Article
  19. Article
  20. Breast tumor-on-chip models: From disease modeling to personalized drug screening.Journal of controlled release : official journal of the Controlled Release Society · 2021
    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

6 authors at 1 institution in 1 country.

Jaclyn A FreudenbergDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104-6082, USA.
Qiang Wang
Makoto Katsumata
Jeffrey Drebin
Izumi Nagatomo
Mark I Greene
University of Pennsylvania · US

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
IMMUNOBIOLOGY OF P185 RECEPTORR01CA055306 · NCI · UNIVERSITY OF PENNSYLVANIA · PI GREENE, MARK I · 1992 to 2011
$2.6M
NCI NIH HHS CA055306NCI NIH HHS R01 CA055306NCI NIH HHS T32 CA009140NCI NIH HHS T32CA09140
6 · The paper itself

Abstract

The HER2 gene encodes the receptor tyrosine kinase HER2 and is often over-expressed or amplified in breast cancer. Up-regulation of HER2 contributes to tumor progression. Many aspects of tumor growth are favorably affected through activation of HER2 signaling. Indeed, HER2 plays a role in increasing proliferation and survival of the primary tumor and distant lesions which upon completion of full transformation cause metastases. P185(HER2/neu) receptors and signaling from them and associated molecules increase motility of both intravasating and extravasating cells, decrease apoptosis, enhance signaling interactions with the microenvironment, regulate adhesion, as well as a multitude of other functions. Recent experimental and clinical evidence supports the view that the spread of incompletely transformed cells occurs at a very early stage in tumor progression. This review concerns the identification and characterization of HER2, the evolution of the metastasis model, and the more recent cancer stem cell model. In particular, we review the evidence for an emerging mechanism of HER2(+) breast cancer progression, whereby the untransformed HER2-expressing cell shows characteristics of stem/progenitor cell, metastasizes, and then completes its final transformation at the secondary site.

Indexed as

Breast NeoplasmsNeoplasm MetastasisAnimalsAntineoplastic AgentsCell Transformation, NeoplasticDisease ProgressionErb-b2 Receptor Tyrosine KinasesErbB ReceptorsFemaleHumansPrecancerous ConditionsSignal TransductionStem CellsAntineoplastic AgentsEGFR protein, humanErb-b2 Receptor Tyrosine KinasesErbB Receptors

Identifiers

PMID19450579
PMCPMC2735009
OpenAlexW1980671878

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.