Evidence map›Paper›PMID 34610416›Full record

ArticleCancer letters2022

MicroRNA-21 deficiency suppresses prostate cancer progression through downregulation of the IRS1-SREBP-1 signaling pathway.

Thanigaivelan Kanagasabai, Guoliang Li, Tian Huai Shen, Nataliya Gladoun, Mireia Castillo-Martin, Sherly I Celada, Yingqiu Xie, Lakendria K Brown, Zaniya A Mark, Josiah Ochieng and 6 more

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
3.9field-weighted citation impact, top 4% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 57 citations in OpenAlex.

  1. Pooled it
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  11. Natural Compounds for Preventing Age-Related Diseases and Cancers.International journal of molecular sciences · 2024
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  18. Decoding the regulatory roles of non-coding RNAs in cellular metabolism and disease.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Review
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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

16 authors at 4 institutions in 1 country.

Thanigaivelan KanagasabaiDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Guoliang LiDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Tian Huai ShenHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, 10032, USA.
Nataliya GladounHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, 10032, USA.
Mireia Castillo-MartinHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, 10032, USA.
Sherly I CeladaDepartment of Biological Sciences, Tennessee State University, Nashville, TN, 37209, USA.
Yingqiu XieDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Lakendria K BrownDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Zaniya A MarkDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Josiah OchiengDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Billy R BallardDepartment of Pathology, Anatomy and Cell Biology, Meharry Medical College, Nashville, TN, 37208, USA.
Carlos Cordon-CardoHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center, New York, NY, 10032, USA.
Samuel E AdunyahDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA.
Renjie JinDepartment of Urology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
Robert J MatusikDepartment of Urology, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
Zhenbang ChenDepartment of Biochemistry, Cancer Biology, Neuroscience and Pharmacology, Meharry Medical College, Nashville, TN, 37208, USA. Electronic address: zchen@mmc.edu.
Meharry Medical College · USColumbia University Irving Medical Center · USVanderbilt University Medical Center · USTennessee State University · US

Funding

The RCMI Program in Health Disparities Research at Meharry Medical College - SupplementU54MD007586 · NIMHD · MEHARRY MEDICAL COLLEGE · PI SANIKA SAMUEL CHIRWA · 2017 to 2026
$48.2M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Technologies and Resources CoreU54MD007593 · NIMHD · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS · 2012 to 2018
$24.7M
Translational Pathology CoreU54CA163069 · NCI · MEHARRY MEDICAL COLLEGE · PI ADUNYAH, SAMUEL EVANS, STEWART, LAMONICA VANETTE · 2011 to 2025
$18.8M
NCATS NIH HHS UL1 TR000445NCI NIH HHS U54 CA163069NIMHD NIH HHS U54 MD007586NIMHD NIH HHS U54 MD007593Wellcome Trust
6 · The paper itself

Abstract

Sterol regulatory element-binding protein 1 (SREBP-1), a master transcription factor in lipogenesis and lipid metabolism, is critical for disease progression and associated with poor outcomes in prostate cancer (PCa) patients. However, the mechanism of SREBP-1 regulation in PCa remains elusive. Here, we report that SREBP-1 is transcriptionally regulated by microRNA-21 (miR-21) in vitro in cultured cells and in vivo in mouse models. We observed aberrant upregulation of SREBP-1, fatty acid synthase (FASN) and acetyl-CoA carboxylase (ACC) in Pten/Trp53 double-null mouse embryonic fibroblasts (MEFs) and Pten/Trp53 double-null mutant mice. Strikingly, miR-21 loss significantly reduced cell proliferation and suppressed the prostate tumorigenesis of Pten/Trp53 mutant mice. Mechanistically, miR-21 inactivation decreased the levels of SREBP-1, FASN, and ACC in human PCa cells through downregulation of insulin receptor substrate 1 (IRS1)-mediated transcription and induction of cellular senescence. Conversely, miR-21 overexpression increased cell proliferation and migration; as well as the levels of IRS1, SREBP-1, FASN, and ACC in human PCa cells. Our findings reveal that miR-21 promotes PCa progression by activating the IRS1/SREBP-1 axis, and targeting miR-21/SREBP-1 signaling pathway can be a novel strategy for controlling PCa malignancy.

Indexed as

Acetyl-CoA CarboxylaseAnimalsCell ProliferationDisease ProgressionFatty Acid Synthase, Type IGene Expression Regulation, NeoplasticHeterograftsHumansInsulin Receptor Substrate ProteinsMaleMiceMicroRNAsProstatic NeoplasmsSignal TransductionSterol Regulatory Element Binding Protein 1ACACA protein, humanAcetyl-CoA CarboxylaseFASN protein, humanFatty Acid Synthase, Type IInsulin Receptor Substrate ProteinsIRS1 protein, humanMicroRNAsMIRN21 microRNA, humanSREBF1 protein, humanSterol Regulatory Element Binding Protein 1ACCFASNFatty acid signaling and mouse modelsPTENTP53

Identifiers

PMID34610416
PMCPMC12419200
OpenAlexW3203222367

What OpenQuestion holds

Textmetadata
LicenceTDM
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.