Evidence map›Paper›PMID 25199985›Full record

ReviewBiochimica et biophysica acta2014

Genetic variation: effect on prostate cancer.

Tristan M Sissung, Douglas K Price, Marzia Del Re, Ariel M Ley, Elisa Giovannetti, William D Figg, Romano Danesi

Open access · greenAbstract readReview
In one paragraph

Review in Biochimica et biophysica acta, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
3.4field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 30 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Assessing the effectiveness of MRI,Polish journal of radiology · 2024
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Genetic Association betweenFrontiers in physiology · 2017
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. 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

7 authors at 3 institutions in 2 countries.

Tristan M SissungNational Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Douglas K PriceNational Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Marzia Del ReDepartment of Clinical and Experimental Medicine, University of Pisa, Italy.
Ariel M LeyNational Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Elisa GiovannettiDepartment of Clinical and Experimental Medicine, University of Pisa, Italy.
William D FiggNational Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
Romano DanesiDepartment of Clinical and Experimental Medicine, University of Pisa, Italy.
University of Pisa · ITNational Cancer Institute · USNational Institutes of Health · US

Funding

Clinical PharmacogeneticsZIABC010627 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 2009 to 2025
$13.9M
Identify SNPs and Polymorphisms Involved in the Development of Prostate CancerZIABC010453 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FIGG, WILLIAM DOUGLAS · 2009 to 2025
$10.4M
Intramural NIH HHS ZIA BC010627
6 · The paper itself

Abstract

The crucial role of androgens in the development of prostate cancer is well established. The aim of this review is to examine the role of constitutional (germline) and tumor-specific (somatic) polymorphisms within important regulatory genes of prostate cancer. These include genes encoding enzymes of the androgen biosynthetic pathway, the androgen receptor gene, genes that encode proteins of the signal transduction pathways that may have a role in disease progression and survival, and genes involved in prostate cancer angiogenesis. Characterization of deregulated pathways critical to cancer cell growth have lead to the development of new treatments, including the CYP17 inhibitor abiraterone and clinical trials using novel drugs that are ongoing or recently completed [1]. The pharmacogenetics of the drugs used to treat prostate cancer will also be addressed. This review will define how germline polymorphisms are known affect a multitude of pathways, and therefore phenotypes, in prostate cancer etiology, progression, and treatment.

Indexed as

Polymorphism, Genetic3-Oxo-5-alpha-Steroid 4-DehydrogenaseAndrogensGenome-Wide Association StudyHumansMaleMembrane ProteinsPharmacogeneticsProstatic NeoplasmsReceptors, Androgen3-Oxo-5-alpha-Steroid 4-DehydrogenaseAndrogensMembrane ProteinsReceptors, AndrogenSRD5A2 protein, humanAndrogen deprivation therapyChemotherapyPharmacogenomicsProstate cancerSteroid

Identifiers

PMID25199985
PMCPMC4260983
OpenAlexW2012403041

What OpenQuestion holds

Textmetadata
LicenceTDM
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.