Evidence map›Paper›PMID 21734453›Full record

ArticleCell cycle (Georgetown, Tex.)2011

JunD-mediated repression of GADD45α and γ regulates escape from cell death in prostate cancer.

Luiz Fernando Zerbini, Jaíra Ferreira de Vasconcellos, Akos Czibere, Yihong Wang, Juliano D Paccez, Xuesong Gu, Jin-Rong Zhou, Towia A Libermann

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. JUNB and JUND in Urological Cancers: A Literature Review.Current issues in molecular biology · 2025
    Review
  2. Review
  3. Article
  4. Alterations in TGFβ signaling during prostate cancer progression.American journal of clinical and experimental urology · 2021
    Review
  5. Article
  6. Article
  7. Inflammatory Serine Proteases Play a Critical Role in the Early Pathogenesis of Diabetic Cardiomyopathy.Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Hepatitis C Virus Increases Free Fatty Acids Absorption and Promotes its Replication Via Down-Regulating GADD45α Expression.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  12. Article
  13. Article
  14. Anticancer drugs for the modulation of endoplasmic reticulum stress and oxidative stress.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2015
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 5 countries.

Luiz Fernando ZerbiniInternational Center for Genetic Engineering and Biotechnology (ICGEB), Cancer Genomics Group, Cape Town, South Africa. luiz.zerbini@uct.ac.za
Jaíra Ferreira de Vasconcellos
Akos Czibere
Yihong Wang
Juliano D Paccez
Xuesong Gu
Jin-Rong Zhou
Towia A Libermann
Hadassah Medical Center · ILBeth Israel Deaconess Medical Center · USCentro de Ingeniería Genética y Biotecnología · CUInternational Centre for Genetic Engineering and Biotechnology · ZAMontefiore Medical Center · US

Funding

Tumor and Circulating Markers as Links Between Obesity and Lethal Prostate CanceP50CA090381 · NCI · DANA-FARBER CANCER INSTITUTE · PI KANTOFF, PHILIP W · 2002 to 2017
$36.2M
Variation in Receptor Tyrosine Kinases and Breast Cancer RiskP50CA089393 · NCI · DANA-FARBER CANCER INSTITUTE · PI WINER, ERIC P · 2000 to 2009
$28.8M
NCI NIH HHS P50 CA089393NCI NIH HHS P50 CA090381NCI NIH HHS P50 CA89393
6 · The paper itself

Abstract

The AP-1 transcription factor complex has been implicated in a variety of biological processes including cell differentiation, proliferation, apoptosis and oncogenic transformation. We previously established that activation of the AP-1 family member JunD contributes to deregulated expression of the anti-apoptotic IL-6 gene in prostate cancer cells. We now show that inhibition of JunD in prostate cancer cells results in GADD45α- and γ-dependent induction of cell death and inhibition of tumor growth that is mediated at least partially via c-Jun N-terminal kinase (JNK) and p38 kinase activation. Apoptosis induction by dominant negative JunD and JNK and p38 kinase activation are impeded upon knock down of GADD45α and γ expression by small interfering RNA, most vividly demonstrating the central role of GADD45α and γ in JunD-mediated escape of prostate cancer cells from programmed cell death.

Indexed as

ApoptosisCell Cycle ProteinsCell Line, TumorGADD45 ProteinsHumansInterleukin-6Intracellular Signaling Peptides and ProteinsMaleMitogen-Activated Protein Kinase 8Nuclear Proteinsp38 Mitogen-Activated Protein KinasesProstatic NeoplasmsProto-Oncogene Proteins c-junRNA InterferenceRNA, Small InterferingCell Cycle ProteinsGADD45A protein, humanGADD45G protein, humanGADD45 ProteinsInterleukin-6Intracellular Signaling Peptides and ProteinsJunD protein, humanMitogen-Activated Protein Kinase 8Nuclear Proteinsp38 Mitogen-Activated Protein KinasesProto-Oncogene Proteins c-junRNA, Small Interfering

Identifiers

PMID21734453
PMCPMC3180197
OpenAlexW2076261981

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.