Evidence map›Paper›PMID 19457610›Full record

ArticleCancer letters2009

Cancer-related transcriptional targets of the circadian gene NPAS2 identified by genome-wide ChIP-on-chip analysis.

Chun-Hui Yi, Tongzhang Zheng, Derek Leaderer, Aaron Hoffman, Yong Zhu

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.7field-weighted citation impact, top 37% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  4. Effect ofFrontiers in endocrinology · 2022
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  7. Review
  8. Article
  9. Article
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  12. A polymorphic GGC repeat in the NPAS2 gene and its association with melanoma.Experimental biology and medicine (Maywood, N.J.) · 2017
    Article
  13. Article
  14. Article
  15. Article
  16. Electric light, particularly at night, disrupts human circadian rhythmicity: is that a problem?Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2015
    Review
  17. Article
  18. Article
  19. Circadian gene variants in cancer.Annals of medicine · 2014
    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

5 authors at 1 institution in 1 country.

Chun-Hui YiDepartment of Epidemiology and Public Health, Yale University School of Medicine, New Haven, CT 06520, United States.
Tongzhang Zheng
Derek Leaderer
Aaron Hoffman
Yong Zhu
Yale University · US

Funding

Database of Functional SNPs in Cancer-Related Environmentally Responsive GenesR01CA122676 · NCI · YALE UNIVERSITY · PI ZHU, YONG · 2007 to 2009
$848k
Methylation Related Genes and Breast Cancer RiskR03CA108369 · NCI · YALE UNIVERSITY · PI ZHU, YONG · 2004 to 2005
$164k
Circadian Genes and Breast CancerR03CA110937 · NCI · YALE UNIVERSITY · PI ZHU, YONG · 2004 to 2005
$164k
NCI NIH HHS CA108369NCI NIH HHS CA110937NCI NIH HHS CA122676NCI NIH HHS R01 CA122676NCI NIH HHS R03 CA108369NCI NIH HHS R03 CA110937
6 · The paper itself

Abstract

The transcription factor NPAS2 is one of nine human core circadian genes that influence a variety of biological processes by regulating the 24-h circadian rhythm. Recently, it has been shown that NPAS2 is a risk biomarker in human cancers and plays a role in tumorigenesis by affecting cancer-related gene expression, and relevant biological pathways. However, it is difficult to study the biological involvement of NPAS2 in cancer development, as little is known about its direct transcriptional targets. The aim of the current study is to create a transcriptional profile of genes regulated by NPAS2, using a human binding ChIP-on-chip analysis of NPAS2 in MCF-7 cells. This genome-wide mapping approach identified 26 genes that contain potential NPAS2 binding regions. Subsequent real-time PCR assays confirmed 16 of these targets, and 9 of these genes (ARHGAP29, CDC25A, CDKN2AIP, CX3CL1, ELF4, GNAL, KDELR1, POU4F2, and THRA) have a known role in tumorigenesis. In addition, a networking analysis of these validated NPAS2 targets revealed that all nine genes, together with REN, are involved in a "Cancer, Cell cycle, Neurological Disease" network. These results report the first list of direct transcriptional targets of NPAS2 and will shed light on the role of circadian genes in tumorigenesis.

Indexed as

Gene Expression ProfilingGene Regulatory NetworksOligonucleotide Array Sequence AnalysisAdenocarcinomaBasic Helix-Loop-Helix ProteinsBreast NeoplasmsCell Line, TumorCell Transformation, NeoplasticChromatin ImmunoprecipitationCircadian RhythmFemaleGene Expression Regulation, NeoplasticGenome-Wide Association StudyHumansNeoplasm ProteinsNerve Tissue ProteinsBasic Helix-Loop-Helix ProteinsNeoplasm ProteinsNerve Tissue ProteinsNPAS2 protein, humanRNA, Small Interfering

Identifiers

PMID19457610
PMCPMC3182267
OpenAlexW2161162458

What OpenQuestion holds

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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.