Evidence map›Paper›PMID 20711217›Full record

ReviewAsian journal of andrology2010

Androgen receptor signaling and mutations in prostate cancer.

Shahriar Koochekpour

Open access · goldAbstract readReview
In one paragraph

Review in Asian journal of andrology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
10.8field-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

71 citing papers in PubMed, 161 citations in OpenAlex.

  1. Sanguinarine chloride exerts its antitumor effects on enzalutamide-resistant prostate cancer by inhibiting cell proliferation and promoting senescence via targeting AR signaling.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Androgen-regulatediScience · 2022
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review

11 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

1 author at 1 institution in 1 country.

Shahriar KoochekpourDepartment of Urology and Stanley S. Scott Cancer Center, School of Medicine, Louisiana State University Health Sciences Center, New Orleans, LA 70112, USA. skooch@lsuhsc.edu
Louisiana State University Health Sciences Center New Orleans · US

Funding

TUMOR MICROENVIRONMENT AND B CELL LYMPHOMASP20RR021970 · NCRR · LSU HEALTH SCIENCES CENTER · PI FOSTER, TIMOTHY C. · 2005 to 2011
$14.1M
Training CoreP20MD004817 · NIMHD · DILLARD UNIVERSITY · PI SOTHERN, MELINDA S · 2010 to 2014
$6.3M
Prosaposin: A Novel Biomarker of Prostate Cancer Progression in African AmericansR01MD005824 · NIMHD · ROSWELL PARK CANCER INSTITUTE CORP · PI KOOCHEKPOUR, SHAHRIAR · 2010 to 2013
$1.5M
Prognostic value of AR mutation in primary African American prostate cancerR21CA143589 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI KOOCHEKPOUR, SHAHRIAR · 2010 to 2011
$353k
Significance of an novel germline AR mutation in black men with prostate cancerR21CA149137 · NCI · ROSWELL PARK CANCER INSTITUTE CORP · PI KOOCHEKPOUR, SHAHRIAR · 2010 to 2011
$335k
NCI NIH HHS R21 CA143589NCI NIH HHS R21-CA143589-01A1NCI NIH HHS R21 CA149137NCI NIH HHS R21-CA149137NCRR NIH HHS 1P20 RR021970NCRR NIH HHS P20 RR021970NIMHD NIH HHS P20 MD004817NIMHD NIH HHS P20MD004817NIMHD NIH HHS R01 MD005824
6 · The paper itself

Abstract

Normal and neoplastic growth of the prostate gland are dependent on androgen receptor (AR) expression and function. Androgenic activation of the AR, in association with its coregulatory factors, is the classical pathway that leads to transcriptional activity of AR target genes. Alternatively, cytoplasmic signaling crosstalk of AR by growth factors, neurotrophic peptides, cytokines or nonandrogenic hormones may have important roles in prostate carcinogenesis and in metastatic or androgen-independent (AI) progression of the disease. In addition, cross-modulation by various nuclear transcription factors acting through basal transcriptional machinery could positively or negatively affect the AR or AR target genes expression and activity. Androgen ablation leads to an initial favorable response in a significant number of patients; however, almost invariably patients relapse with an aggressive form of the disease known as castration-resistant or hormone-refractory prostate cancer (PCa). Understanding critical molecular events that lead PCa cells to resist androgen-deprivation therapy is essential in developing successful treatments for hormone-refractory disease. In a significant number of hormone-refractory patients, the AR is overexpressed, mutated or genomically amplified. These genetic alterations maintain an active presence for a highly sensitive AR, which is responsive to androgens, antiandrogens or nonandrogenic hormones and collectively confer a selective growth advantage to PCa cells. This review provides a brief synopsis of the AR structure, AR coregulators, posttranslational modifications of AR, duality of AR function in prostate epithelial and stromal cells, AR-dependent signaling, genetic changes in the form of somatic and germline mutations and their known functional significance in PCa cells and tissues.

Indexed as

AnimalsBlack PeopleGene ExpressionHumansMaleMutationProstatic NeoplasmsReceptors, AndrogenTranscriptional ActivationTranscription FactorsWhite PeopleReceptors, AndrogenTranscription Factors

Identifiers

PMID20711217
PMCPMC3006239
OpenAlexW2165854061

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.