Evidence map›Paper›PMID 21886458›Full record

ArticleJournal of carcinogenesis2011

Androgen receptor signaling in prostate cancer development and progression.

Peter E Lonergan, Donald J Tindall

Open access · goldAbstract read
In one paragraph

Article in Journal of carcinogenesis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 288 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
288citing papers in PubMed, 3 pooled it
17.0field-weighted citation impact, top 1% 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

288 citing papers in PubMed, 3 syntheses or guidelines pooled it, 538 citations in OpenAlex.

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228 more citing papers are in PubMed but not listed here.

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

2 authors at 1 institution in 1 country.

Peter E LonerganDepartment of Urology, Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minnesota, United States of America.
Donald J Tindall
Mayo Clinic · US

Funding

Utility of serum and Tissue Biomarkers for Predicting Response to Androgen DeprivP50CA091956 · NCI · MAYO CLINIC ROCHESTER · PI TINDALL, DONALD J. · 2001 to 2010
$23.4M
Coregulators in Androgen-Refractory Prostate CancerR01CA121277 · NCI · MAYO CLINIC ROCHESTER · PI TINDALL, DONALD J. · 2006 to 2010
$1.3M
Androgenic Inactivation of FOXO1 in Prostate CancerR01CA125747 · NCI · MAYO CLINIC ROCHESTER · PI TINDALL, DONALD J. · 2007 to 2011
$1.3M
NCI NIH HHS P50 CA091956NCI NIH HHS R01 CA121277NCI NIH HHS R01 CA125747
6 · The paper itself

Abstract

The androgen receptor (AR) signaling axis plays a critical role in the development, function and homeostasis of the prostate. The classical action of AR is to regulate gene transcriptional processes via AR nuclear translocation, binding to androgen response elements on target genes and recruitment of, or crosstalk with, transcription factors. Prostate cancer initiation and progression is also uniquely dependent on AR. Androgen deprivation therapy remains the standard of care for treatment of advanced prostate cancer. Despite an initial favorable response, almost all patients invariably progress to a more aggressive, castrate-resistant phenotype. Considerable evidence now supports the concept that development of castrate-resistant prostate cancer (CRPC) is causally related to continued transactivation of AR. Understanding the critical events and complexities of AR signaling in the progression to CRPC is essential in developing successful future therapies. This review provides a synopsis of AR structure and signaling in prostate cancer progression, with a special focus on recent findings on the role of AR in CRPC. Clinical implications of these findings and potential directions for future research are also outlined.

Indexed as

Androgen receptorcastrate-resistant prostate cancersignaling

Identifiers

PMID21886458
PMCPMC3162670
OpenAlexW1996956937

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.