Evidence map›Paper›PMID 37761978›Full record

ReviewInternational journal of molecular sciences2023

Targeting Key Players of Neuroendocrine Differentiation in Prostate Cancer.

Irene Zamora, Michael R Freeman, Ignacio J Encío, Mirja Rotinen

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 13 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

4 authors at 2 institutions in 2 countries.

Irene ZamoraDepartment of Health Science, Public University of Navarre, 31008 Pamplona, Spain.ORCID 0009-0004-4723-9403
Michael R FreemanDepartments of Urology and Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA.
Ignacio J EncíoDepartment of Health Science, Public University of Navarre, 31008 Pamplona, Spain.ORCID 0000-0003-1732-1989
Mirja RotinenDepartment of Health Science, Public University of Navarre, 31008 Pamplona, Spain.ORCID 0000-0002-0755-8360
Universidad Publica de Navarra · ESCedars-Sinai Medical Center · US

Funding

Department of Health, Government of Navarre 026/2022Spanish Ministry of Science, Innovation and Universities PID2019-109577RA-I00/AEI/10.13039/501100011033Spanish Ministry of Science, Innovation and Universities (Ramón y Cajal Program) RYC-2018-023874-I
6 · The paper itself

Abstract

Neuroendocrine prostate cancer (NEPC) is a highly aggressive subtype of prostate cancer (PC) that commonly emerges through a transdifferentiation process from prostate adenocarcinoma and evades conventional therapies. Extensive molecular research has revealed factors that drive lineage plasticity, uncovering novel therapeutic targets to be explored. A diverse array of targeting agents is currently under evaluation in pre-clinical and clinical studies with promising results in suppressing or reversing the neuroendocrine phenotype and inhibiting tumor growth and metastasis. This new knowledge has the potential to contribute to the development of novel therapeutic approaches that may enhance the clinical management and prognosis of this lethal disease. In the present review, we discuss molecular players involved in the neuroendocrine phenotype, and we explore therapeutic strategies that are currently under investigation for NEPC.

Indexed as

Carcinoma, NeuroendocrineProstatic NeoplasmsCell Line, TumorHumansMalePhenotypelineage plasticityneuroendocrine transdifferentiationprostate cancertargeted therapy

Identifiers

PMID37761978
PMCPMC10531052
OpenAlexW4386440070

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.