Evidence map›Paper›PMID 33805919›Full record

ReviewBiomolecules2021

Current Status and Future Perspectives of Androgen Receptor Inhibition Therapy for Prostate Cancer: A Comprehensive Review.

Tae Jin Kim, Young Hwa Lee, Kyo Chul Koo

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
4.8field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 38 citations in OpenAlex.

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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 2 institutions in 1 country.

Tae Jin KimCHA Bundang Medical Center, Department of Urology, CHA University College of Medicine, Seongnam 13496, Korea.ORCID 0000-0001-7836-1998
Young Hwa LeeDepartment of Urology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul 06229, Korea.
Kyo Chul KooDepartment of Urology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul 06229, Korea.ORCID 0000-0001-7303-6256
Yonsei University · KRCHA University Bundang Medical Center · KR

Funding

Gangnam Severance Hospital Prostate Cancer Center Research Committee 7523110National Research Foundation of Korea 2020R1F1A1073833
6 · The paper itself

Abstract

The androgen receptor (AR) is one of the main components in the development and progression of prostate cancer (PCa), and treatment strategies are mostly directed toward manipulation of the AR pathway. In the metastatic setting, androgen deprivation therapy (ADT) is the foundation of treatment in patients with hormone-sensitive prostate cancer (HSPC). However, treatment response is short-lived, and the majority of patients ultimately progress to castration-resistant prostate cancer (CRPC). Surmountable data from clinical trials have shown that the maintenance of AR signaling in the castration environment is accountable for disease progression. Study results indicate multiple factors and survival pathways involved in PCa. Based on these findings, the alternative molecular pathways involved in PCa progression can be manipulated to improve current regimens and develop novel treatment modalities in the management of CRPC. In this review, the interaction between AR signaling and other molecular pathways involved in tumor pathogenesis and its clinical implications in metastasis and advanced disease will be discussed, along with a thorough overview of current and ongoing novel treatments for AR signaling inhibition.

Indexed as

Androgen Receptor AntagonistsBenzamidesHumansMaleNeoplasm MetastasisNitrilesPhenylthiohydantoinProstatic NeoplasmsReceptors, AndrogenSignal TransductionSurvival AnalysisTumor MicroenvironmentAndrogen Receptor AntagonistsBenzamidesenzalutamideNitrilesPhenylthiohydantoinReceptors, Androgenandrogen deprivation therapyandrogen receptorandrogen receptor inhibitionprostate cancer

Identifiers

PMID33805919
PMCPMC8064397
OpenAlexW3145040485

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.