Evidence map›Paper›PMID 17334399›Full record

ArticleOncogene2007

Functional consequences of cyclin D1/BRCA1 interaction in breast cancer cells.

K Kehn, R Berro, A Alhaj, M E Bottazzi, W-I Yeh, Z Klase, R Van Duyne, S Fu, F Kashanchi

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.3field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 51 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. miR-20a/Foxj2 Axis Mediates Growth and Metastasis of Colorectal Cancer Cells as Identified by Integrated Analysis.Medical science monitor : international medical journal of experimental and clinical research · 2020
    Article
  8. OncoTargets and therapy · 2017
    Article
  9. Article
  10. Article
  11. Article
  12. Cyclin D2 is a GATA4 cofactor in cardiogenesis.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  13. Cyclin D1 determines estrogen signaling in the mammary gland in vivo.Molecular endocrinology (Baltimore, Md.) · 2013
    Article
  14. Article
  15. Review
  16. Cyclin D as a therapeutic target in cancer.Nature reviews. Cancer · 2011
    Review
  17. Article
  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

9 authors at 2 institutions in 2 countries.

K KehnDepartment of Biochemistry and Molecular Biology, The George Washington University, Washington, DC 20037, USA.
R Berro
A Alhaj
M E Bottazzi
W-I Yeh
Z Klase
R Van Duyne
S Fu
F Kashanchi
George Washington University · USHuman Genome Sciences (United States) · US

Funding

HIV1 INHIBITION USING TAT PEPTIDE DERIVATIVESR01AI043894 · NIAID · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI KASHANCHI, FATAH · 1999 to 2015
$4.4M
Effect on cdk inhibitor in HIV-1 replicationR21AI065236 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI KASHANCHI, FATAH · 2006 to 2007
$415k
NIAID NIH HHS AI043894NIAID NIH HHS AI065236
6 · The paper itself

Abstract

The inheritance of one defective BRCA1 or BRCA2 allele predisposes an individual to developing breast and ovarian cancers. BRCA1 is a multifunctional tumor suppressor protein, which through interaction with a vast array of proteins has implications in processes such as cell cycle, transcription, DNA damage response and chromatin remodeling. Conversely, the oncogene, cyclin D1 is overexpressed in about 35% of all breast cancer cases. In this study, we provide detailed analyses on the phosphorylation state of BRCA1 by cyclin D1/cdk4 complexes. In particular, we have identified Ser 632 of BRCA1 as a cyclin D1/cdk4 phosphorylation site in vitro. Using chromatin immunoprecipitation assays, we observed that the inhibition of cyclin D1/cdk4 activity resulted in increased BRCA1 DNA binding at particular promoters in vivo. In addition, we identified multiple novel genes that are bound by BRCA1 in vivo. Collectively, these results indicate that cyclin D1/cdk4-mediated phosphorylation of BRCA1 inhibits the ability of BRCA1 to be recruited to particular promoters in vivo. Therefore, cyclin D1/Cdk4 phosphorylation of BRCA1 could provide a mechanism to interfere with the DNA-dependent activities of BRCA1.

Indexed as

Amino Acid SequenceBRCA1 ProteinBreast NeoplasmsCell CycleCell Line, TumorChromatin ImmunoprecipitationCyclin D1Cyclin-Dependent Kinase 4DNAG1 PhaseGene Expression Regulation, NeoplasticHumansMolecular Sequence DataPhosphorylationPromoter Regions, GeneticResting Phase, Cell CycleBRCA1 ProteinCyclin D1Cyclin-Dependent Kinase 4DNA

Identifiers

PMID17334399
OpenAlexW2056914311

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.