Evidence map›Paper›PMID 26039627›Full record

ArticlePloS one2015

E2F1-Mediated Induction of NFYB Attenuates Apoptosis via Joint Regulation of a Pro-Survival Transcriptional Program.

Xiaolei Jiang, Joseph Roy Nevins, Igor Shats, Jen-Tsan Chi

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

10 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  4. Translational cancer research · 2022
    Article
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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

4 authors at 2 institutions in 1 country.

Xiaolei JiangDuke Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America; Department of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina, United States of America.
Joseph Roy NevinsDepartment of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina, United States of America.
Igor ShatsDuke Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America; Department of Biomedical Engineering, Duke University Medical Center, Durham, North Carolina, United States of America.
Jen-Tsan ChiDuke Center for Genomic and Computational Biology, Duke University, Durham, North Carolina, United States of America; Department of Molecular Genetics and Microbiology, Duke University, Durham, North Carolina, United States of America.
Duke University · USDuke Medical Center · US

Funding

Gene expression programs of lactic acidosis in human cancersR01CA125618 · NCI · DUKE UNIVERSITY · PI CHI, JEN-TSAN ASHLEY · 2007 to 2016
$3.3M
Oncogenic Gene Regulatory NetworksR01CA106520 · NCI · DUKE UNIVERSITY · PI CHI, JEN-TSAN ASHLEY · 2005 to 2014
$2.9M
NCI NIH HHS CA106520NCI NIH HHS CA125618NCI NIH HHS R01 CA106520NCI NIH HHS R01 CA125618
6 · The paper itself

Abstract

The E2F1 transcription factor regulates cell proliferation and apoptosis through the control of a considerable variety of target genes. Previous work has detailed the role of other transcription factors in mediating the specificity of E2F function. Here we identify the NF-YB transcription factor as a novel direct E2F1 target. Genome-wide expression analysis of the effects of NFYB knockdown on E2F1-mediated transcription identified a large group of genes that are co-regulated by E2F1 and NFYB. We also provide evidence that knockdown of NFYB enhances E2F1-induced apoptosis, suggesting a pro-survival function of the NFYB/E2F1 joint transcriptional program. Bioinformatic analysis suggests that deregulation of these NFY-dependent E2F1 target genes might play a role in sarcomagenesis as well as drug resistance.

Indexed as

ApoptosisTranscription, GeneticCCAAT-Binding FactorCell Line, TumorCell SurvivalDrug Resistance, NeoplasmE2F1 Transcription FactorGene Expression ProfilingGene Expression Regulation, NeoplasticHumansSarcomaTranscriptional ActivationUp-RegulationCCAAT-Binding FactorE2F1 Transcription FactorNFYB protein, human

Identifiers

PMID26039627
PMCPMC4454684
OpenAlexW1525887571

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.