Evidence map›Paper›PMID 37455903›Full record

ReviewFrontiers in endocrinology2023

Lineage plasticity and treatment resistance in prostate cancer: the intersection of genetics, epigenetics, and evolution.

Jarrell Imamura, Shinjini Ganguly, Andrew Muskara, Ross S Liao, Jane K Nguyen, Christopher Weight, Christopher E Wee, Shilpa Gupta, Omar Y Mian

Abstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing 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

48 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

9 authors.

Jarrell ImamuraTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.
Shinjini GangulyTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.
Andrew MuskaraTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.
Ross S LiaoGlickman Urologic Institute, Cleveland Clinic, Cleveland, OH, United States.
Jane K NguyenGlickman Urologic Institute, Cleveland Clinic, Cleveland, OH, United States.
Christopher WeightGlickman Urologic Institute, Cleveland Clinic, Cleveland, OH, United States.
Christopher E WeeTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.
Shilpa GuptaTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.
Omar Y MianTaussig Cancer Institute, Cleveland Clinic, Cleveland, OH, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Androgen deprivation therapy is a cornerstone of treatment for advanced prostate cancer, and the development of castrate-resistant prostate cancer (CRPC) is the primary cause of prostate cancer-related mortality. While CRPC typically develops through a gain in androgen receptor (AR) signaling, a subset of CRPC will lose reliance on the AR. This process involves genetic, epigenetic, and hormonal changes that promote cellular plasticity, leading to AR-indifferent disease, with neuroendocrine prostate cancer (NEPC) being the quintessential example. NEPC is enriched following treatment with second-generation anti-androgens and exhibits resistance to endocrine therapy. Loss of

Indexed as

Prostatic Neoplasms, Castration-ResistantAndrogen AntagonistsEpigenesis, GeneticHumansMaleProstateReceptors, AndrogenAndrogen AntagonistsReceptors, Androgenepigenetic dysregulationhormone therapy resistancelineage plasticityneuroendocrine prostate cancerradioresistance

Identifiers

PMID37455903
PMCPMC10349394

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.