Evidence map›Paper›PMID 40203114›Full record

ArticleScience advances2025

Androgen receptor-regulated lncRNA PRCAT71 promotes AR signaling through the interaction with KHSRP in prostate cancer.

Yongyong Yang, Ting-You Wang, Qianru Li, Jiawen Lu, Yanan Ren, Adam B Weiner, Joshua Fry, Qi Liu, Chaehyun Yum, Rui Wang and 8 more

Abstract read
In one paragraph

Article in Science advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
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

18 authors.

Yongyong YangDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0003-2297-5848
Ting-You WangDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0003-4354-3198
Qianru LiDepartment of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-4193-1675
Jiawen LuDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-4815-8574
Yanan RenDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0001-9586-3690
Adam B WeinerDepartment of Urology, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA 90095, USA.ORCID 0000-0002-1912-042X
Joshua FryDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-2503-611X
Qi LiuDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-7652-4201
Chaehyun YumDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Rui WangDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Qingxiang GuoDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-3694-3428
Yu WanDepartment of Biomedical Engineering, Northwestern University McCormick School of Engineering, Evanston, IL 60628, USA.
Zhe JiDepartment of Pharmacology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-1809-8099
Xuesen DongVancouver Prostate Centre, Vancouver General Hospital, Vancouver, BC V6H 3Z6, Canada.ORCID 0000-0002-3115-3371
Tamara L LotanDepartment of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA.
Edward M SchaefferDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.
Rendong YangDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-9512-2240
Qi CaoDepartment of Urology, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.ORCID 0000-0002-5140-3681

Funding

Targeting FOXA1-downstream pathways: a novel therapeutic strategy for castration-resistant prostate cancerP50CA180995 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI ABDULKADIR, SARKI A., HUSSAIN, MAHA H · 2015 to 2025
$19.9M
A novel role for EZH2 in PARP regulation and PARPi-resistance in prostate cancerR01CA285684 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Qi Cao, HENGYAO NIU · 2024 to 2026
$2.9M
A non-canonical role for EZH2 in rRNA methtlationR01CA256741 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI CAO, QI · 2021 to 2025
$2.1M
Characterizing functional translation in putative 'noncoding' regions of a genome: Admin SupplR35GM138192 · NIGMS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI JI, ZHE · 2020 to 2024
$2.1M
Computational approaches to delineate non-canonical splicing eventsR35GM142441 · NIGMS · UNIVERSITY OF MINNESOTA · PI YANG, RENDONG · 2021 to 2025
$2.0M
Genome-wide mapping and characterization of exitrons in human cancerR01CA259388 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Rendong Yang · 2022 to 2026
$1.8M
NCI NIH HHS P50 CA180995NCI NIH HHS R01 CA256741NCI NIH HHS R01 CA259388NCI NIH HHS R01 CA285684NIGMS NIH HHS R35 GM138192NIGMS NIH HHS R35 GM142441
6 · The paper itself

Abstract

Mounting evidence indicates that long noncoding RNAs (lncRNAs) play vital roles in tumorigenesis and progression of cancers. However, the functions and regulatory mechanisms of lncRNAs in prostate cancer (PCa) are still largely unknown. In this study, we found an lncRNA, PCa-associated transcript 71 (PRCAT71), highly expressed in metastatic and primary PCa compared to benign prostate tissues. Silencing PRCAT71 inhibited cancerous properties of PCa cells and androgen receptor (AR) signaling. Mechanistically, PRCAT71 acts as a scaffold to recruit K homology (KH)-type splicing regulatory protein (KHSRP) to AR messenger RNA (mRNA) and stabilize AR mRNA, leading to activated AR signaling. KHSRP plays a critical role in PCa progression. PRCAT71 is transcriptionally regulated by AR-driven enhancers, forming a positive regulatory loop between AR and PRCAT71 in PCa. Our study demonstrates a coordinated regulation of AR mRNA by lncRNA PRCAT71 and RNA binding protein KHSRP and provides insight that the PRCAT71-KHSRP-AR axis is a promising therapeutic target for treating PCa.

Indexed as

Prostatic NeoplasmsReceptors, AndrogenRNA-Binding ProteinsRNA, Long NoncodingSignal TransductionCell Line, TumorGene Expression Regulation, NeoplasticHumansMaleRNA, MessengerTrans-ActivatorsAR protein, humanKHSRP protein, humanReceptors, AndrogenRNA-Binding ProteinsRNA, Long NoncodingRNA, MessengerTrans-Activators

Identifiers

PMID40203114
PMCPMC11980854

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.