Evidence map›Paper›PMID 37973913›Full record

ArticleNature communications2023

SND1 binds to ERG and promotes tumor growth in genetic mouse models of prostate cancer.

Sheng-You Liao, Dmytro Rudoy, Sander B Frank, Luan T Phan, Olga Klezovitch, Julian Kwan, Ilsa Coleman, Michael C Haffner, Dapei Li, Peter S Nelson and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

13 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
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  5. mActa pharmaceutica Sinica. B · 2025
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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

12 authors at 5 institutions in 2 countries.

Sheng-You LiaoDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0003-2057-3167
Dmytro RudoyDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Sander B FrankDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0001-7591-944X
Luan T PhanDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Olga KlezovitchDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Julian KwanCenter for Network Systems Biology, Departments of Biochemistry & Biology, Boston University, Boston, MA, USA.
Ilsa ColemanDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Michael C HaffnerDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.
Dapei LiDepartment of Medicine, Division of Medical Oncology, University of Washington, Seattle, WA, USA.
Peter S NelsonDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA.ORCID 0000-0002-5451-5726
Andrew EmiliCenter for Network Systems Biology, Departments of Biochemistry & Biology, Boston University, Boston, MA, USA.ORCID 0000-0001-8995-246X
Valeri VasioukhinDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, WA, USA. vvasiouk@fredhutch.org.ORCID 0000-0002-6730-0281
Fred Hutch Cancer Center · USBoston University · USUniversity of Washington · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAUniversity of Washington Medical Center · US

Funding

Translational Bioimaging Core Shared ResourceP30CA015704 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Eric Collisson · 1985 to 2026
$296.4M
TRANSCRIPTOME AND PROTEOME STRATIFICATION OF PROSTATE ADENOCARCINOMA PHENOTYPESP50CA097186 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PETER S NELSON · 2002 to 2026
$58.1M
Steroid Metabolism in Castration-Resistant Prostate CancerP01CA163227 · NCI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI PETER S NELSON · 2013 to 2026
$25.0M
Tryptophan Metabolism in Human Brain TumorsR01CA123451 · NCI · WAYNE STATE UNIVERSITY · PI JUHASZ, CSABA, MITTAL, SANDEEP · 2008 to 2018
$3.1M
The Hippo Pathway in Prostate Gland Homeostasis and Prostate CancerR01CA176844 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI VASIOUKHIN, VALERI · 2013 to 2017
$1.8M
NCI NIH HHS P01 CA163227NCI NIH HHS P30 CA015704NCI NIH HHS P50 CA097186NCI NIH HHS R01 CA123451NCI NIH HHS R01 CA176844
6 · The paper itself

Abstract

SND1 and MTDH are known to promote cancer and therapy resistance, but their mechanisms and interactions with other oncogenes remain unclear. Here, we show that oncoprotein ERG interacts with SND1/MTDH complex through SND1's Tudor domain. ERG, an ETS-domain transcription factor, is overexpressed in many prostate cancers. Knocking down SND1 in human prostate epithelial cells, especially those overexpressing ERG, negatively impacts cell proliferation. Transcriptional analysis shows substantial overlap in genes regulated by ERG and SND1. Mechanistically, we show that ERG promotes nuclear localization of SND1/MTDH. Forced nuclear localization of SND1 prominently increases its growth promoting function irrespective of ERG expression. In mice, prostate-specific Snd1 deletion reduces cancer growth and tumor burden in a prostate cancer model (PB-Cre/Pten

Indexed as

Prostatic NeoplasmsAnimalsCell Transformation, NeoplasticEndonucleasesERG1 Potassium ChannelGene Expression Regulation, NeoplasticHumansMaleMembrane ProteinsMiceProstateRNA-Binding ProteinsTranscriptional Regulator ERGTranscription FactorsTudor DomainEndonucleasesERG1 Potassium ChannelERG protein, humanKcnh2 protein, mouseMembrane ProteinsMTDH protein, humanRNA-Binding ProteinsSND1 protein, humanSnd1 protein, mouseTranscriptional Regulator ERGTranscription Factors

Identifiers

PMID37973913
PMCPMC10654515
OpenAlexW4388718466

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.