Evidence map›Paper›PMID 14982856›Full record

ArticleThe American journal of pathology2004

The role of the cyclin D1-dependent kinases in ErbB2-mediated breast cancer.

Chuanwei Yang, Viviana Ionescu-Tiba, Karen Burns, Michelle Gadd, Lawrence Zukerberg, David N Louis, Dennis Sgroi, Emmett V Schmidt

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The American journal of pathology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02947685 (A Randomized, Open Label, Phase III Trial to Evaluate the Efficacy and Safety of Palbociclib + Anti-HER2 Therapy + Endocrine Therapy vs. Anti-HER2 Therapy + Endocrine Therapy After Induction Treatment for Hormone Receptor Positive), which is not on this map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.2field-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.

NCT02947685 phase3active not recruitingnot on this mapstarted 2017, after this paper: background citation

A Randomized, Open Label, Phase III Trial to Evaluate the Efficacy and Safety of Palbociclib + Anti-HER2 Therapy + Endocrine Therapy vs. Anti-HER2 Therapy + Endocrine Therapy After Induction Treatment for Hormone Receptor Positive (HR+)/HER2-Positive Metastatic Breast Cancer

TypeinterventionalSponsorAlliance Foundation Trials, LLC.Ran2017 to 2026Enrolled518ConditionsHER-2 Positive Breast Cancer, Estrogen Receptor Positive Breast CancerArmspalbociclib, trastuzumab, pertuzumab, letrozole, Anastrozole
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. ETS-targeted therapy: can it substitute for MEK inhibitors?Clinical and translational medicine · 2017
    Review
  6. Clinical applications of mouse models for breast cancer engaging HER2/neu.Integrative cancer science and therapeutics · 2016
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Cyclin D as a therapeutic target in cancer.Nature reviews. Cancer · 2011
    Review
  12. Article
  13. Article
  14. Nuclear cyclin D1: an oncogenic driver in human cancer.Journal of cellular physiology · 2009
    Review
  15. 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 4 institutions in 3 countries.

Chuanwei YangMassachusetts General Hospital (MGH) Cancer Research Center, Massachusetts General Hospital, Boston, Massachusetts 02114, USA.
Viviana Ionescu-Tiba
Karen Burns
Michelle Gadd
Lawrence Zukerberg
David N Louis
Dennis Sgroi
Emmett V Schmidt
Massachusetts General Hospital · USCenter for Cancer Research · USOttawa Hospital · CASociety of Surgical Oncology · US

Funding

Variation in Receptor Tyrosine Kinases and Breast Cancer RiskP50CA089393 · NCI · DANA-FARBER CANCER INSTITUTE · PI HARRIS, LYNDSAY NORINE · 2000 to 2009
$28.8M
FUNCTIONS OF CYCLIN D1 IN BREAST CANCERR01CA069069 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI SCHMIDT, EMMETT VANCE · 1997 to 2007
$2.5M
NCI NIH HHS P50 CA089393NCI NIH HHS P50 CA89393NCI NIH HHS R01 CA069069NCI NIH HHS R01 CA69069
6 · The paper itself

Abstract

Intact cyclin D1 functions are essential for transformation by erbB2 in tissue culture and murine models. Because cyclin D1 may alter cell proliferation through a variety of mechanisms, we used transgenic models and human tumor samples to particularly address the role of cyclin D1-cyclin-dependent kinases in transformation by erbB2. The p16 tumor suppressor specifically blocks cyclin-dependent kinase 4 and 6 activity. Here we show that an MMTV-p16 transgene blocked tumorigenesis by erbB2, demonstrating that deregulation of the cyclin-dependent kinase partner of cyclin D1 is an essential target of erbB2. ErbB2 overexpression was a determining factor in deregulation of cyclin D1-cdk4/6 interactions because neither transgenic cyclin D1 nor loss of p16 accelerated tumorigenesis in MMTV-erbB2-transgenic mice. ErbB2 was also a deciding factor in deregulation of cyclin D1-cdk4/6 in human tumors because no loss of pRb or p16 was found in tumors overexpressing erbB2, although erbB2-negative invasive breast adenocarcinomas frequently lacked expression of p16 or pRb. We conclude that deregulation of cyclin D1-Cdk4/6 interactions is a critical target of erbB2 function in human and mouse breast tumors, and erbB2's overexpression may be sufficient to deregulate cyclin D1-cdk4/6 activity in breast cancer.

Indexed as

Proto-Oncogene ProteinsAnimalsBreast NeoplasmsCDC2 Protein KinaseCyclin D1Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent KinasesDNA PrimersGenes, erbB-2Genes, p16HumansImmunohistochemistryMembrane ProteinsMiceMice, TransgenicCDC2 Protein KinaseCDK4 protein, humanCdk4 protein, mouseCDK6 protein, humanCdk6 protein, mouseCyclin D1Cyclin-Dependent Kinase 4Cyclin-Dependent Kinase 6Cyclin-Dependent KinasesDNA PrimersFam89b protein, mouseMembrane ProteinsProto-Oncogene ProteinsReceptors, Virus

Identifiers

PMID14982856
PMCPMC1614725
OpenAlexW2035073888

What OpenQuestion holds

Textmetadata
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.