Evidence map›Paper›PMID 25940700›Full record

ArticleOncotarget2015

Kinase-independent role of cyclin D1 in chromosomal instability and mammary tumorigenesis.

Mathew C Casimiro, Gabriele Di Sante, Marco Crosariol, Emanuele Loro, William Dampier, Adam Ertel, Zuoren Yu, Elizabeth A Saria, Alexandros Papanikolaou, Zhiping Li and 9 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

33 citing papers in PubMed, 45 citations in OpenAlex.

  1. Article
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  8. CCND1 and FGFR1 gene amplifications are associated with reduced benefit from aromatase inhibitors in metastatic breast cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2021
    Article
  9. A Cyclin D1-Dependent Transcriptional Program Predicts Clinical Outcome in Mantle Cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. The double dealing of cyclin D1.Cell cycle (Georgetown, Tex.) · 2020
    Review
  16. Article
  17. Review
  18. Article
  19. Review
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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

19 authors at 5 institutions in 2 countries.

Mathew C CasimiroDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Gabriele Di SanteDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Marco CrosariolDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Emanuele LoroDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
William DampierCenter for Integrated Bioinformatics, School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA 19104, USA.
Adam ErtelDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Zuoren YuDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Elizabeth A SariaCenter for Molecular Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Alexandros PapanikolaouCenter for Molecular Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Zhiping LiDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Chenguang WangStem Cell and Regenerative Medicine, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Sankar AddyaDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Michael P LisantiStem Cell and Regenerative Medicine, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Paolo FortinaDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Robert D CardiffDepartment of Pathology and Laboratory Medicine, UC Davis Center for Comparative Medicine, University of California, Davis CA 95616, USA.
Aydin TozerenCenter for Integrated Bioinformatics, School of Biomedical Engineering, Science and Health Systems, Drexel University, Philadelphia, PA 19104, USA.
Erik S KnudsenDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Andrew ArnoldCenter for Molecular Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Richard G PestellDepartments of Cancer Biology, Thomas Jefferson University & Hospital, Philadelphia, PA 19107, USA.
Thomas Jefferson University Hospital · USSidney Kimmel Cancer Center · USUConn Health · USDrexel University · USUniversity of California, Davis · US

Funding

X-Ray Crystallography and Macromolecular CharacterizationP30CA056036 · NCI · THOMAS JEFFERSON UNIVERSITY · PI CHRISTINE M. EISCHEN · 1995 to 2026
$94.8M
Initiation and Maintenance In Mammary TumorigenesisR01CA075503 · NCI · YESHIVA UNIVERSITY · PI PESTELL, RICHARD G · 1998 to 2011
$4.6M
CYCLIN D1 FUNCTION IN PROSTATE CANCERR01CA086072 · NCI · YESHIVA UNIVERSITY · PI PESTELL, RICHARD G · 2001 to 2013
$3.3M
REGULATION OF CYCLIN D1 EXPRESSIONR01CA070896 · NCI · YESHIVA UNIVERSITY · PI PESTELL, RICHARD G · 2000 to 2010
$3.2M
NOVEL CYCLIN-LIKE CANDIDATE ONCOGENE ON 11Q13R01CA055909 · NCI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI ARNOLD, ANDREW · 1992 to 2005
$1.2M
NCI NIH HHS P30 CA056036NCI NIH HHS P30CA56036NCI NIH HHS R01 CA055909NCI NIH HHS R01 CA070896NCI NIH HHS R01 CA075503NCI NIH HHS R01 CA086072NCI NIH HHS R01 CA12934NCI NIH HHS [R01CA55909NCI NIH HHS [R01CA70896NCI NIH HHS R01CA75503NCI NIH HHS R01CA86072
6 · The paper itself

Abstract

Cyclin D1 is an important molecular driver of human breast cancer but better understanding of its oncogenic mechanisms is needed, especially to enhance efforts in targeted therapeutics. Currently, pharmaceutical initiatives to inhibit cyclin D1 are focused on the catalytic component since the transforming capacity is thought to reside in the cyclin D1/CDK activity. We initiated the following study to directly test the oncogenic potential of catalytically inactive cyclin D1 in an in vivo mouse model that is relevant to breast cancer. Herein, transduction of cyclin D1(-/-) mouse embryonic fibroblasts (MEFs) with the kinase dead KE mutant of cyclin D1 led to aneuploidy, abnormalities in mitotic spindle formation, autosome amplification, and chromosomal instability (CIN) by gene expression profiling. Acute transgenic expression of either cyclin D1(WT) or cyclin D1(KE) in the mammary gland was sufficient to induce a high CIN score within 7 days. Sustained expression of cyclin D1(KE) induced mammary adenocarcinoma with similar kinetics to that of the wild-type cyclin D1. ChIP-Seq studies demonstrated recruitment of cyclin D1(WT) and cyclin D1(KE) to the genes governing CIN. We conclude that the CDK-activating function of cyclin D1 is not necessary to induce either chromosomal instability or mammary tumorigenesis.

Indexed as

AdenocarcinomaAmino Acid SubstitutionAneuploidyAnimalsCatalytic DomainCells, CulturedCell Transformation, NeoplasticCentrosomeChromosomal InstabilityCyclin D1FemaleFibroblastsGenes, bcl-1HumansMammary Neoplasms, ExperimentalMammary Tumor Virus, MouseCCND1 protein, humanCcnd1 protein, mouseCyclin D1palbociclibPiperazinesPyridinesRecombinant Fusion Proteinsbreast cancerchromosomal instabilitycyclin D1

Identifiers

PMID25940700
PMCPMC4496164
OpenAlexW2120861858

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.