Evidence map›Paper›PMID 20019190›Full record

ArticleThe American journal of pathology2010

The Sex-determining region Y-box 4 and homeobox C6 transcriptional networks in prostate cancer progression: crosstalk with the Wnt, Notch, and PI3K pathways.

Carlos S Moreno

Open access · bronzeAbstract readLecture
In one paragraph

Article in The American journal of pathology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 3 pooled it
3.8field-weighted citation impact, top 7% 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

40 citing papers in PubMed, 3 syntheses or guidelines pooled it, 67 citations in OpenAlex.

  1. SOX4 is a potential prognostic factor in human cancers: a systematic review and meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2016
    Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
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  9. Alterations in TGFβ signaling during prostate cancer progression.American journal of clinical and experimental urology · 2021
    Review
  10. Article
  11. SOX4 is activated by C-MYC in prostate cancer.Medical oncology (Northwood, London, England) · 2019
    Article
  12. Article
  13. Article
  14. SOX11: friend or foe in tumor prevention and carcinogenesis?Therapeutic advances in medical oncology · 2019
    Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. SOXC Genes and the Control of Skeletogenesis.Current osteoporosis reports · 2016
    Review
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

1 author at 1 institution in 1 country.

Carlos S MorenoDepartment of Pathology and Laboratory Medicine, Winship Cancer Institute, Atlanta, GA 30322, USA. cmoreno@emory.edu
Piedmont Cancer Institute · US

Funding

Developmental Transcription Factors in Prostate CancerR01CA106826 · NCI · EMORY UNIVERSITY · PI MORENO, CARLOS SANCHEZ · 2005 to 2013
$2.6M
NCI NIH HHS R01 CA106826
6 · The paper itself

Abstract

The transforming growth factor beta, Hedgehog, Notch, and Wnt signaling pathways all play critical roles in the development and progression of prostate cancer. It is becoming increasingly apparent that these pathways may intersect with developmentally important transcription factors such as the sex-determining region Y-box 4 (SOX4), homeobox C6, enhancer of zeste 2, and ETS-related gene, which are up-regulated in prostate cancers. For example, identification of the downstream targets of SOX4 and homeobox C6 suggests that these factors may cooperate to activate the Notch pathway and the PI3K/AKT pathway, possibly in response to Wnt signals. PI3K/AKT activation likely occurs indirectly via up-regulation of growth factor receptors, while Notch activation is secondary to up-regulation of Notch pathway components. In addition, SOX4 may affect terminal differentiation via regulation of other transcription factors such as NKX3.1 and MLL, and regulation of components of the microRNA pathway such as Dicer and Argonaute 1. The evidence supporting activation of these pathways in prostate cancer progression suggests that combinations of compounds targeting them may be of benefit to patients with aggressive, metastatic disease.

Indexed as

Gene Regulatory NetworksAwards and PrizesCarcinomaDisease ProgressionHomeodomain ProteinsHumansMaleModels, BiologicalPhosphatidylinositol 3-KinasesProstatic NeoplasmsReceptor Cross-TalkReceptors, NotchSignal TransductionSOXC Transcription FactorsTranscription, GeneticWnt ProteinsHomeodomain ProteinsPhosphatidylinositol 3-KinasesReceptors, NotchSOX4 protein, humanSOXC Transcription FactorsWnt Proteins

Identifiers

PMID20019190
PMCPMC2808058
OpenAlexW128803419

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.