Evidence map›Paper›PMID 37976356›Full record

ArticleScience advances2023

The SMYD3-MAP3K2 signaling axis promotes tumor aggressiveness and metastasis in prostate cancer.

Sabeen Ikram, Apurv Rege, Maraki Y Negesse, Alexandre G Casanova, Nicolas Reynoird, Erin M Green

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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  10. Genetic Alterations ofInternational journal of molecular sciences · 2024
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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

6 authors at 3 institutions in 2 countries.

Sabeen IkramDepartment of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD, USA.ORCID 0009-0002-1856-8393
Apurv RegeDepartment of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD, USA.
Maraki Y NegesseDepartment of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD, USA.ORCID 0000-0002-2818-285X
Alexandre G CasanovaGrenoble Alpes University, CNRS UMR5309, INSERM U1209, Institute for Advanced Biosciences, Grenoble, France.ORCID 0000-0003-2988-2046
Nicolas ReynoirdGrenoble Alpes University, CNRS UMR5309, INSERM U1209, Institute for Advanced Biosciences, Grenoble, France.ORCID 0000-0003-1578-2781
Erin M GreenDepartment of Biological Sciences, University of Maryland Baltimore County, Baltimore, MD, USA.ORCID 0000-0003-3923-6726
University of Maryland, Baltimore County · USCentre National de la Recherche Scientifique · FRUniversity of Maryland, Baltimore · US

Funding

EXPAND PARTICIPATION BY MINORITIES IN BIOMEDICAL SCIENCER25GM055036 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SUMMERS, MICHAEL FINLEY · 1996 to 2021
$16.9M
Graduate Training at The Chemistry Biology InterfaceT32GM066706 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI SELEY-RADTKE, KATHERINE L, SMITH, AARON T · 2004 to 2023
$3.3M
Lysine methylation at chromatin and cellular responses to stressR01GM124342 · NIGMS · UNIVERSITY OF MARYLAND BALTIMORE COUNTY · PI GREEN, ERIN · 2017 to 2021
$1.5M
NIGMS NIH HHS R01 GM124342NIGMS NIH HHS R25 GM055036NIGMS NIH HHS T32 GM066706
6 · The paper itself

Abstract

Aberrant activation of Ras/Raf/mitogen-activated protein kinase (MAPK) signaling is frequently linked to metastatic prostate cancer (PCa); therefore, the characterization of modulators of this pathway is critical for defining therapeutic vulnerabilities for metastatic PCa. The lysine methyltransferase SET and MYND domain 3 (SMYD3) methylates MAPK kinase kinase 2 (MAP3K2) in some cancers, causing enhanced activation of MAPK signaling. In PCa, SMYD3 is frequently overexpressed and associated with disease severity; however, its molecular function in promoting tumorigenesis has not been defined. We demonstrate that SMYD3 critically regulates tumor-associated phenotypes via its methyltransferase activity in PCa cells and mouse xenograft models. SMYD3-dependent methylation of MAP3K2 promotes epithelial-mesenchymal transition associated behaviors by altering the abundance of the intermediate filament vimentin. Furthermore, activation of the SMYD3-MAP3K2 signaling axis supports a positive feedback loop continually promoting high levels of SMYD3. Our data provide insight into signaling pathways involved in metastatic PCa and enhance understanding of mechanistic functions for SMYD3 to reveal potential therapeutic opportunities for PCa.

Indexed as

Prostatic NeoplasmsAnimalsCarcinogenesisCell Line, TumorCell Transformation, NeoplasticGene Expression Regulation, NeoplasticHistone-Lysine N-MethyltransferaseHumansMaleMAP Kinase Kinase Kinase 2MethyltransferasesMiceMitogen-Activated Protein KinasesSignal TransductionHistone-Lysine N-MethyltransferaseMAP3K2 protein, humanMAP Kinase Kinase Kinase 2MethyltransferasesMitogen-Activated Protein KinasesSMYD3 protein, human

Identifiers

PMID37976356
PMCPMC10656069
OpenAlexW4388757430

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.