Evidence map›Paper›PMID 36263323›Full record

ReviewFrontiers in endocrinology2022

Exploring anti-androgen therapies in hormone dependent prostate cancer and new therapeutic routes for castration resistant prostate cancer.

Anna E Harris, Veronika M Metzler, Jennifer Lothion-Roy, Dhruvika Varun, Corinne L Woodcock, Daisy B Haigh, Chantelle Endeley, Maria Haque, Michael S Toss, Mansour Alsaleem and 17 more

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

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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

27 authors.

Anna E HarrisUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Veronika M MetzlerUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Jennifer Lothion-RoyUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Dhruvika VarunUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Corinne L WoodcockUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Daisy B HaighUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Chantelle EndeleyUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Maria HaqueUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Michael S TossUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Mansour AlsaleemUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Jenny L PerssonDepartment of Molecular Biology, Umeå University, Umeå, Sweden.
Lorraine J GudasDepartment of Pharmacology, Weill Cornell Medicine, New York, NY, United States.
Emad RakhaUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Brian D RobinsonDepartment of Urology, Weill Cornell Medicine, New York, NY, United States.
Francesca KhaniDepartment of Urology, Weill Cornell Medicine, New York, NY, United States.
Laura M MartinEnglander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, United States.
Jenna E MoyerEnglander Institute for Precision Medicine, Weill Cornell Medicine, New York, NY, United States.
Juliette BrownlieUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Srinivasan MadhusudanUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Cinzia AllegrucciUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Victoria H JamesUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Catrin S RutlandUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Rupert G FraySchool of Biosciences, University of Nottingham, Nottingham, United Kingdom.
Atara NtekimDepartment of Oncology, University Hospital Ibadan, Ibadan, Nigeria.
Simone de BrotComparative Pathology Platform (COMPATH), Institute of Animal Pathology, University of Bern, Bern, Switzerland.
Nigel P MonganUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.
Jennie N JeyapalanUniversity of Nottingham Biodiscovery Institute, University of Nottingham, University Park, Nottingham, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Androgen deprivation therapies (ADTs) are important treatments which inhibit androgen-induced prostate cancer (PCa) progression by either preventing androgen biosynthesis (e.g. abiraterone) or by antagonizing androgen receptor (AR) function (e.g. bicalutamide, enzalutamide, darolutamide). A major limitation of current ADTs is they often remain effective for limited durations after which patients commonly progress to a lethal and incurable form of PCa, called castration-resistant prostate cancer (CRPC) where the AR continues to orchestrate pro-oncogenic signalling. Indeed, the increasing numbers of ADT-related treatment-emergent neuroendocrine-like prostate cancers (NePC), which lack AR and are thus insensitive to ADT, represents a major therapeutic challenge. There is therefore an urgent need to better understand the mechanisms of AR action in hormone dependent disease and the progression to CRPC, to enable the development of new approaches to prevent, reverse or delay ADT-resistance. Interestingly the AR regulates distinct transcriptional networks in hormone dependent and CRPC, and this appears to be related to the aberrant function of key AR-epigenetic coregulator enzymes including the lysine demethylase 1 (LSD1/KDM1A). In this review we summarize the current best status of anti-androgen clinical trials, the potential for novel combination therapies and we explore recent advances in the development of novel epigenetic targeted therapies that may be relevant to prevent or reverse disease progression in patients with advanced CRPC.

Indexed as

Prostatic Neoplasms, Castration-ResistantReceptors, AndrogenAndrogen AntagonistsAndrogensHistone DemethylasesHumansLysineMaleAndrogen AntagonistsAndrogensHistone DemethylasesKDM1A protein, humanLysineReceptors, Androgenanti-androgencastration resistant prostate cancerepigenetic targeted treatmentPARP inhibitorsTherapy

Identifiers

PMID36263323
PMCPMC9575553

What Socratic 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 Socratic graph.