Evidence map›Paper›PMID 21037926›Full record

ReviewOncotarget2010

The Siah2-HIF-FoxA2 axis in prostate cancer – new markers and therapeutic opportunities.

Jianfei Qi, Maurizio Pellecchia, Ze'ev A Ronai

Open access · hybridAbstract readReview
In one paragraph

Review in Oncotarget, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

22 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. mMolecular therapy. Nucleic acids · 2022
    Article
  6. Article
  7. Focus on the tumor microenvironment: A seedbed for neuroendocrine prostateFrontiers in cell and developmental biology · 2022
    Review
  8. Article
  9. Genome-Based Classification and Therapy of Prostate Cancer.Diagnostics (Basel, Switzerland) · 2018
    Review
  10. Article
  11. Article
  12. Review
  13. Two high-resolution structures of the human E3 ubiquitin ligase Siah1.Acta crystallographica. Section F, Structural biology and crystallization communications · 2013
    Article
  14. Regulators and effectors of Siah ubiquitin ligases.Cell biochemistry and biophysics · 2013
    Review
  15. Article
  16. Review
  17. Article
  18. The "Sharp" blade against HIF-mediated metastasis.Cell cycle (Georgetown, Tex.) · 2012
    Article
  19. 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

3 authors at 1 institution in 1 country.

Jianfei QiSignal Transduction Program, Sanford-Burnham Medical Research Institute, La Jolla, CA 92037, USA.
Maurizio Pellecchia
Ze'ev A Ronai
Sanford Burnham Prebys Medical Discovery Institute · US

Funding

Tumor Assessment CoreP01CA128814 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI SMITH, JEFFREY W · 2009 to 2020
$19.1M
Novel Insights in the regulation of HIF1alpha StabilityR01CA111515 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI RONAI, ZEEV A. · 2004 to 2014
$3.8M
NCI NIH HHS CA111515NCI NIH HHS CA128814NCI NIH HHS P01 CA128814NCI NIH HHS R01 CA111515
6 · The paper itself

Abstract

Recent studies indicate the importance of the ubiquitin ligase Siah2 in control of more aggressive prostate tumors – namely, neuroendocrine (NE) prostate tumors and prostate adenocarcinoma (PCa) harboring neuroendocrine lesions. Siah2-dependent expression and activity of HIF-1α regulate its availability to form a transcriptional complex with FoxA2, resulting in expression of specific target genes, including Hes6, Sox9 and Jmjd1a, whose co-expression is sufficient for formation of NE tumors and NE lesions in PCa. These studies provide novel markers to diagnose and monitor formation of NE lesions and NE tumors. Furthermore, defining the regulatory axis consisting of Siah2 and HIF-1α/FoxA2 cooperation suggests novel therapeutic modalities to treat these most aggressive forms of prostate cancer. Here we review current understanding of Siah role in control of hypoxia and prostate tumor development and highlight potential approaches for targeting components along Siah-regulated pathways.

Indexed as

Signal TransductionAdenocarcinomaAnimalsAntineoplastic AgentsBiomarkers, TumorDrug DesignGene Expression Regulation, NeoplasticHepatocyte Nuclear Factor 3-betaHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMolecular Targeted TherapyNeuroendocrine TumorsNuclear ProteinsProstatic NeoplasmsSeven in Absentia ProteinsAntineoplastic AgentsBiomarkers, TumorFOXA2 protein, humanHepatocyte Nuclear Factor 3-betaHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitNuclear ProteinsSeven in Absentia ProteinsUbiquitin-Protein Ligases

Identifiers

PMID21037926
PMCPMC2964873
OpenAlexW1821453853

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.