Evidence map›Paper›PMID 32902124›Full record

ArticleJournal of cellular and molecular medicine2020

The AKR1C3/AR-V7 complex maintains CRPC tumour growth by repressing B4GALT1 expression.

Bin Wang, Shiqi Wu, Yong Fang, Guangxi Sun, Dalin He, Jer-Tsong Hsieh, Xinyang Wang, Hao Zeng, Kaijie Wu

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 15% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

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  17. Dysregulated androgen synthesis and anti-androgen resistance in advanced prostate cancer.American journal of clinical and experimental urology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Bin WangDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.ORCID 0000-0002-2662-1986
Shiqi WuDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Yong FangDepartment of Urology, The East Division of First Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Guangxi SunDepartment of Urology, West China Hospital of Sichuan University, Chengdu, China.
Dalin HeDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Jer-Tsong HsiehDepartment of Urology, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Xinyang WangDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Hao ZengDepartment of Urology, West China Hospital of Sichuan University, Chengdu, China.
Kaijie WuDepartment of Urology, First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
First Affiliated Hospital of Xi'an Jiaotong University · CNSichuan University · CNSun Yat-sen University · CNThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple mechanisms contribute to the survival and growth of metastatic castration-resistant prostate cancer (mCRPC) cells without androgen, including androgen receptor splice variants (AR-V) and de novo intratumoral androgen synthesis. AKR1C3 is a critical androgenic enzyme that plays different roles in mCRPC, such as an EMT driver or AR coactivator. However, the relationship and regulatory mechanisms between AKR1C3 and AR-V remain largely unknown. In this study, we observed a positive correlation between AKR1C3 and AR-V7 staining in tissues from prostate rebiopsy at mCRPC. Mechanistically, AKR1C3 interacts with AR-V7 protein in CRPC cells, which can reciprocally inhibit AR-V7 and AKR1C3 protein degradation. Biologically, this complex is essential for in vitro and in vivo tumour growth of CRPC cells after androgen deprivation as it represses B4GALT1, a unique tumour suppressor gene in PCa. Together, this study reveals AKR1C3/AR-V7 complex as a potential therapeutic target in mCRPC.

Indexed as

Gene Expression Regulation, NeoplasticAgedAldo-Keto Reductase Family 1 Member C3AnimalsCell Line, TumorCell ProliferationGalactosyltransferasesHEK293 CellsHumansMaleMice, Inbred BALB CMice, NudeModels, BiologicalProstatic Neoplasms, Castration-ResistantProtein BindingProtein StabilityAKR1C3 protein, humanAldo-Keto Reductase Family 1 Member C3AR protein, humanbeta-1,4-galactosyltransferase IGalactosyltransferasesReceptors, AndrogenUbiquitinAKR1C3AR-V7B4GALT1castration-resistant prostate cancercomplex

Identifiers

PMID32902124
PMCPMC7579719
OpenAlexW3084802165

What OpenQuestion holds

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Registered trials

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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.