Evidence map›Paper›PMID 26325261›Full record

ReviewOncotarget2015

Adaptive responses of androgen receptor signaling in castration-resistant prostate cancer.

Sven Perner, Marcus V Cronauer, Andres Jan Schrader, Helmut Klocker, Zoran Culig, Aria Baniahmad

Open access · diamondAbstract readReview
In one paragraph

Review in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
8.6field-weighted citation impact, top 2% 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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Radionuclides Landscape in Prostate Cancer Theranostics.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. Role of Circular RNAs in Prostate Cancer.Current medicinal chemistry · 2024
    Review
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Review
  18. Review
  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

6 authors at 5 institutions in 2 countries.

Sven PernerSection for Prostate Cancer Research, Institute of Pathology, Center for Integrated Oncology Cologne/Bonn, University Hospital of Bonn, Bonn, Germany.
Marcus V CronauerDepartment of Urology, Ulm University Medical Center, Ulm, Germany.
Andres Jan SchraderDepartment of Urology, Muenster University Medical Center, Münster, Germany.
Helmut KlockerDivision of Experimental Urology, Department of Urology, Medical University of Innsbruck, Innsbruck, Austria.
Zoran CuligDepartment of Urology, Medical University of Innsbruck, Innsbruck, Austria.
Aria BaniahmadInstitute of Human Genetics, Jena University Hospital, Jena, Germany.
Innsbruck Medical University · ATJena University Hospital · DEUniversität Innsbruck · ATUniversität Ulm · DEUniversity Hospital Bonn · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate Cancer (PCa) is an important age-related disease being the most common cancer malignancy and the second leading cause of cancer mortality in men in Western countries. Initially, PCa progression is androgen receptor (AR)- and androgen-dependent. Eventually advanced PCa reaches the stage of Castration-Resistant Prostate Cancer (CRPC), but remains dependent on AR, which indicates the importance of AR activity also for CRPC. Here, we discuss various pathways that influence the AR activity in CRPC, which indicates an adaptation of the AR signaling in PCa to overcome the treatment of PCa. The adaptation pathways include interferences of the normal regulation of the AR protein level, the expression of AR variants, the crosstalk of the AR with cytokine tyrosine kinases, the Src-Akt-, the MAPK-signaling pathways and AR corepressors. Furthermore, we summarize the current treatment options with regard to the underlying molecular basis of the common adaptation processes of AR signaling that may arise after the treatment with AR antagonists, androgen deprivation therapy (ADT) as well as for CRPC, and point towards novel therapeutic strategies. The understanding of individualized adaptation processes in PCa will lead to individualized treatment options in the future.

Indexed as

Androgen Receptor AntagonistsAnimalsCarcinogenesisCytokinesGene Expression Regulation, NeoplasticHumansMaleMutationPolymorphism, GeneticPrecision MedicineProstatic Neoplasms, Castration-ResistantReceptor Cross-TalkReceptors, AndrogenSignal TransductionAndrogen Receptor AntagonistsCytokinesReceptors, Androgenandrogen receptorprostate cancer

Identifiers

PMID26325261
PMCPMC4742123
OpenAlexW1688964160

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.