Evidence map›Paper›PMID 41772945›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

GNL3 Orchestrates AR Transcriptional Programs to Drive Castration-Resistant Prostate Cancer and Immune Evasion.

Cuiting Zhang, Tin Long Cheong, Nitin Narwade, Dandan Dong, Mokan Deng, Zhengqiang Miao, Zhaoqiang Ding, Wenchao Li, Kate Man Kei Lei, Gong-Hong Wei and 3 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

13 authors.

Cuiting ZhangCancer Centre, University of Macau, Taipa, Macau SAR, China.
Tin Long CheongCancer Centre, University of Macau, Taipa, Macau SAR, China.
Nitin NarwadeCancer Centre, University of Macau, Taipa, Macau SAR, China.
Dandan DongFudan University Shanghai Cancer Center & MOE Key Laboratory of Metabolism and Molecular Medicine, Department of Biochemistry and Molecular Biology of School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.
Mokan DengCancer Centre, University of Macau, Taipa, Macau SAR, China.
Zhengqiang MiaoGenomics, Bioinformatics & Single Cell Core, Faculty of Health Sciences, University of Macau, Taipa, Macau SAR, China.
Zhaoqiang DingCancer Centre, University of Macau, Taipa, Macau SAR, China.
Wenchao LiDepartment of Urology, Zhongda Hospital Southeast University, Nanjing, Jiangsu, China.
Kate Man Kei LeiCancer Centre, University of Macau, Taipa, Macau SAR, China.
Gong-Hong WeiFudan University Shanghai Cancer Center & MOE Key Laboratory of Metabolism and Molecular Medicine, Department of Biochemistry and Molecular Biology of School of Basic Medical Sciences, Shanghai Medical College of Fudan University, Shanghai, China.
Terence Chuen Wai PoonCancer Centre, University of Macau, Taipa, Macau SAR, China.
Chu-Xia DengCancer Centre, University of Macau, Taipa, Macau SAR, China.
Edwin CheungCancer Centre, University of Macau, Taipa, Macau SAR, China.ORCID https://orcid.org/0000-0001-8034-2833

Funding

Macau Science and Technology Development Fund 0009/2022/AKPMacau Science and Technology Development Fund 0030/2025/AMJMacau Science and Technology Development Fund 0054/2023/RIA1Macau Science and Technology Development Fund 0129/2024/RIA2Macau Science and Technology Development Fund 0137/2020/A3University of Macau MYRG2022-00204-FHSUniversity of Macau MYRG-GRG2023-00189-FHS-UMDFUniversity of Macau MYRG-GRG2024-00178-FHS
6 · The paper itself

Abstract

Androgen receptor (AR) signaling is a primary oncogenic driver of castration-resistant prostate cancer (CRPC), yet the mechanism remains incompletely understood. Through proteomic profiling of CRPC and primary PCa cells, we identify G Protein Nucleolar 3 (GNL3) as a novel AR coregulator. GNL3 physically interacts with AR, enhances its chromatin occupancy, and directly coactivates transcriptional programs that promote cell proliferation, including NEK2 and CDC20. Concurrently, GNL3 functions as a corepressor of immune-responsive genes such as CXCL10 and TAP1 via class I histone deacetylases (HDACs), thereby facilitating CD8+ T cell elimination and establishing an immunosuppressive tumor microenvironment. GNL3 expression and AR-GNL3 complex formation progressively increase from normal prostate to CRPC and correlate with poor clinical outcomes. Functionally, GNL3 knockdown sensitizes CRPC cells to AR antagonists and impairs tumor growth and metastasis. Furthermore, we demonstrate that combinatorial inhibition of NEK2, class I HDACs, and AR signaling can be a potential therapeutic strategy for CRPC. Overall, these findings establish GNL3 as a dual-function AR coregulator and therapeutic target, providing mechanistic insights into transcriptional regulation and immune evasion in advanced PCa.

Indexed as

Immune EvasionNuclear ProteinsProstatic Neoplasms, Castration-ResistantReceptors, AndrogenAnimalsCell Line, TumorGene Expression Regulation, NeoplasticHumansMaleMiceSignal TransductionTumor MicroenvironmentAR protein, humanNuclear ProteinsReceptors, AndrogenAR coregulatorcastration‐resistant prostate cancerGNL3immunosuppression

Identifiers

PMID41772945
PMCPMC13159112

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.