Evidence map›Paper›PMID 41162153›Full record

ArticleGenes & development2026

ERRγ impedes neuroendocrine prostate cancer development.

Ting Li, Catherine R Dufour, Lingwei Han, Anthony Alfonso, Mirna Farhat, Annabelle Beaumier, Qian Chen, Jin-Jian Lu, Vincent Giguère

Abstract read
In one paragraph

Article in Genes & development, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ting LiGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada; vincent.giguere@mcgill.ca tingli@um.edu.mo.ORCID 0000-0001-8733-4625
Catherine R DufourGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada.ORCID 0000-0001-7324-3458
Lingwei HanGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada.ORCID 0000-0001-5842-5501
Anthony AlfonsoGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada.ORCID 0009-0004-8650-8530
Mirna FarhatGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada.ORCID 0009-0004-8778-6604
Annabelle BeaumierGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada.
Qian ChenMinistry of Education Frontiers Science Center for Precision Oncology, University of Macau, Macao SAR 999078, China.
Jin-Jian LuState Key Laboratory of Mechanism and Quality of Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau, Macao SAR 999078, China.
Vincent GiguèreGoodman Cancer Institute, McGill University, Montréal, Québec H3A 1A3, Canada; vincent.giguere@mcgill.ca tingli@um.edu.mo.ORCID 0000-0001-9567-3694

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuroendocrine prostate cancer (NEPC) is a lethal subtype of castration-resistant prostate cancer (CRPC). The molecular mechanisms underlying the progression of CRPC toward NEPC remain incompletely understood, and effective treatments remain to be discovered. Here, we report that loss of the nuclear receptor ERRγ promotes neuroendocrine differentiation in a Pten-deficient mouse model of prostate adenocarcinoma. These findings were recapitulated in advanced cellular and xenograft models of human prostate cancer. Critically, we show that ERRγ gain of function can reverse instilled NEPC features accompanied by suppression of growth and oncogenic metabolic reprogramming. Activation of a neuroendocrine transcriptional program enabled by ERRγ deficiency unveiled a targetable vulnerability exploited by the combined pharmacological inhibition of EZH2 and RET kinase that effectively inhibited the growth of ERRγ-deficient tumor organoids and cells. Collectively, our findings demonstrate that ERRγ downregulation facilitates prostate cancer adeno-to-neuroendocrine transformation and offer potential therapeutic strategies to prevent/treat the development of poor outcome NEPC.

Indexed as

Carcinoma, NeuroendocrineProstatic NeoplasmsReceptors, EstrogenAnimalsCell DifferentiationCell Line, TumorDisease Models, AnimalGene Expression Regulation, NeoplasticHumansMaleMicePTEN PhosphohydrolaseESRRG protein, humanEsrrg protein, mousePTEN PhosphohydrolaseReceptors, EstrogenadenocarcinomaChIP-seqEZH2lineage plasticitymetabolismNEPCnuclear receptorPROX1RETRNA-seqtranscription

Identifiers

PMID41162153
PMCPMC12863258

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.