Evidence map›Paper›PMID 23318451›Full record

ArticleOncogene2014

TRIM3, a tumor suppressor linked to regulation of p21(Waf1/Cip1.).

Y Liu, R Raheja, N Yeh, D Ciznadija, A M Pedraza, T Ozawa, E Hukkelhoven, H Erdjument-Bromage, P Tempst, N P Gauthier and 3 more

Abstract read
In one paragraph

Article in Oncogene, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

35 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Review
  7. TRIM56 promotes malignant progression of glioblastoma by stabilizing cIAP1 protein.Journal of experimental & clinical cancer research : CR · 2022
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. miR-4513 promotes breast cancer progression through targeting TRIM3.American journal of translational research · 2019
    Article
  19. Article
  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

13 authors at 3 institutions in 2 countries.

Y LiuPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
R RahejaPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
N YehPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
D CiznadijaPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
A M PedrazaHuman Oncology and Pathogenesis, New York, NY, USA.
T OzawaCancer Biology, New York, NY, USA.
E HukkelhovenPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
H Erdjument-BromagePrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
P TempstPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
N P GauthierComputational Biology. Memorial Sloan Kettering Cancer Center, New York, NY, USA.
C BrennanHuman Oncology and Pathogenesis, New York, NY, USA.
E C HollandCancer Biology, New York, NY, USA.
A KoffPrograms in Molecular Biology, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Memorial Sloan Kettering Cancer Center · USCentre for Cancer Biology · AUNew York Oncology Hematology · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
P27KIP1 EXPRESSION, A PROGNOSTIC INDICATOR==BUT WHY?R01CA089563 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI KOFF, ANDREW · 2001 to 2011
$4.2M
NCI NIH HHS CA89563NCI NIH HHS P30 CA008748NCI NIH HHS P30CA08748NCI NIH HHS R01 CA089563
6 · The paper itself

Abstract

The TRIM family of genes is largely studied because of their roles in development, differentiation and host cell antiviral defenses; however, roles in cancer biology are emerging. Loss of heterozygosity of the TRIM3 locus in ∼20% of human glioblastomas raised the possibility that this NHL-domain containing member of the TRIM gene family might be a mammalian tumor suppressor. Consistent with this, reducing TRIM3 expression increased the incidence of and accelerated the development of platelet-derived growth factor -induced glioma in mice. Furthermore, TRIM3 can bind to the cdk inhibitor p21(WAF1/CIP1). Thus, we conclude that TRIM3 is a tumor suppressor mapping to chromosome 11p15.5 and that it might block tumor growth by sequestering p21 and preventing it from facilitating the accumulation of cyclin D1-cdk4.

Indexed as

AnimalsCarrier ProteinsCell LineCell Line, TransformedCell Line, TumorCyclin-Dependent Kinase Inhibitor p21Gene Expression Regulation, NeoplasticGlioblastomaHumansImmunoblottingLoss of HeterozygosityMiceMice, KnockoutMutationProtein BindingRNA InterferenceCarrier ProteinsCyclin-Dependent Kinase Inhibitor p21RNA, MessengerTRIM3 protein, humanTRIM3 protein, mouseTumor Suppressor Proteins

Identifiers

PMID23318451
PMCPMC3928554
OpenAlexW2011744268

What Socratic 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 Socratic graph.