Evidence map›Paper›PMID 28459432›Full record

ArticleOncogenesis2017

Metformin inhibits SUV39H1-mediated migration of prostate cancer cells.

T Yu, C Wang, J Yang, Y Guo, Y Wu, X Li

Open access · goldAbstract read
In one paragraph

Article in Oncogenesis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

37 citing papers in PubMed, 65 citations in OpenAlex.

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  11. [Research Progress of Role and Mechanism of SETD7 in Tumor Occurrence 
and Progression].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2023
    Article
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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 4 institutions in 2 countries.

T YuInstitute of Gene Engineered Animal Models for Human Diseases, Dalian Medical University, Dalian, China.
C WangBiochemistry Section, Surgical Neurology Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, USA.ORCID http://orcid.org/0000-0001-6015-6806
J YangDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry (NYUCD), New York, NY, USA.
Y GuoDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry (NYUCD), New York, NY, USA.
Y WuInstitute of Gene Engineered Animal Models for Human Diseases, Dalian Medical University, Dalian, China.
X LiDepartment of Basic Science and Craniofacial Biology, New York University College of Dentistry (NYUCD), New York, NY, USA.
Dalian Medical University · CNNew York University · USNational Institutes of Health · USNYU Langone Health · US

Funding

(PQA1) Novel epigenetic mechanism mediate metformin inhibition of prostate cancerR01CA180277 · NCI · NEW YORK UNIVERSITY · PI LI, XIN · 2013 to 2016
$1.1M
Metformin as a novel chemopreventive agent for prostate cancerR03CA172894 · NCI · NEW YORK UNIVERSITY · PI LI, XIN · 2013 to 2014
$156k
NCI NIH HHS R01 CA180277NCI NIH HHS R03 CA172894
6 · The paper itself

Abstract

Prostate cancer (PCa) is a leading cause of cancer-related death among men, largely due to incurable distant metastases. Metformin, the most common used anti-type-2 diabetes medicine, has been linked to reduced cancer risk and better diagnosis. We found that metformin was able to inhibit PCa cell migration, which correlates with tumor metastatic capability. The pathogenesis and progression of tumors are closely related to dysregulated gene expression in tumor cells through epigenetic alterations such as DNA methylation and histone modifications. We found that the level of SUV39H1, a histone methyltransferase of H3 Lys9, was reduced in metformin-treated PCa cells in a time-dependent manner. SUV39H1 overexpression increased PCa migration, whereas SUV39H1 depletion suppressed PCa cell migration. There is a positive correlation between SUV39H1 expression and PCa pathological stages. We further showed that both metformin treatment and SUV39H1 knockout in PCa cells can reduce integrin αV and β1 proteins, as well as their downstream phosphorylated focal adhesion kinase (FAK) levels, which is essential for functional adhesion signaling and tumor cell migration. Taken together, metformin reduced SUV39H1 to inhibit migration of PCa cells via disturbing the integrin-FAK signaling. Our study suggests SUV39H1 as a novel target to inhibit PCa cell migration.

Identifiers

PMID28459432
PMCPMC5523061
OpenAlexW2611799052

What OpenQuestion holds

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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.