Evidence map›Paper›PMID 23308284›Full record

ArticlePloS one2013

The induction of microRNA-16 in colon cancer cells by protein arginine deiminase inhibition causes a p53-dependent cell cycle arrest.

Xiangli Cui, Erin E Witalison, Alena P Chumanevich, Alexander A Chumanevich, Deepak Poudyal, Venkataraman Subramanian, Aaron J Schetter, Curtis C Harris, Paul R Thompson, Lorne J Hofseth

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

24 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Low miR-16 expression induces regulatory CD4American journal of cancer research · 2021
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  16. Article
  17. Characterization of antiproliferative potential and biological targets of a copper compound containing 4'-phenyl terpyridine.Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry · 2015
    Article
  18. Article
  19. Article
  20. Inhibiting protein arginine deiminases has antioxidant consequences.The Journal of pharmacology and experimental therapeutics · 2015
    Article
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

10 authors at 5 institutions in 2 countries.

Xiangli CuiDepartment of Drug Discovery and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, Columbia, South Carolina, United States of America.
Erin E Witalison
Alena P Chumanevich
Alexander A Chumanevich
Deepak Poudyal
Venkataraman Subramanian
Aaron J Schetter
Curtis C Harris
Paul R Thompson
Lorne J Hofseth
University of South Carolina · USScripps Research Institute · USCenter for Cancer Research · USNational Cancer Institute · USShanxi Medical University · CN

Funding

p53, Aging, and CancerZIABC011496 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HARRIS, CURTIS · 2013 to 2025
$21.1M
Use of Resveratrol to treat experimental multiple sclerosisP01AT003961 · NCCIH · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI NAGARKATTI, PRAKASH S · 2007 to 2018
$14.2M
Haloacetamidine based inactivators of Protein Arginine Deiminase 4R01GM079357 · NIGMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI THOMPSON, PAUL R · 2007 to 2016
$3.3M
Targeting Protein Arginine Deiminases to Prevent Colitis and Colon CancerR01CA151304 · NCI · UNIVERSITY OF SOUTH CAROLINA AT COLUMBIA · PI HOFSETH, LORNE J, THOMPSON, PAUL R · 2011 to 2015
$1.6M
NCCIH NIH HHS P01 AT003961NCI NIH HHS 5R01CA151304NCI NIH HHS R01 CA151304NIGMS NIH HHS R01 GM079357
6 · The paper itself

Abstract

Protein Arginine Deiminases (PADs) catalyze the post-translational conversion of peptidyl-Arginine to peptidyl-Citrulline in a calcium-dependent, irreversible reaction. Evidence is emerging that PADs play a role in carcinogenesis. To determine the cancer-associated functional implications of PADs, we designed a small molecule PAD inhibitor (called Chor-amidine or Cl-amidine), and tested the impact of this drug on the cell cycle. Data derived from experiments in colon cancer cells indicate that Cl-amidine causes a G1 arrest, and that this was p53-dependent. In a separate set of experiments, we found that Cl-amidine caused a significant increase in microRNA-16 (miRNA-16), and that this increase was also p53-dependent. Because miRNA-16 is a putative tumor suppressor miRNA, and others have found that miRNA-16 suppresses proliferation, we hypothesized that the p53-dependent G1 arrest associated with PAD inhibition was, in turn, dependent on miRNA-16 expression. Results are consistent with this hypothesis. As well, we found the G1 arrest is at least in part due to the ability of Cl-amidine-mediated expression of miRNA-16 to suppress its' G1-associated targets: cyclins D1, D2, D3, E1, and cdk6. Our study sheds light into the mechanisms by which PAD inhibition can protect against or treat colon cancer.

Indexed as

AmidinesCell Cycle CheckpointsCell Line, TumorColonic NeoplasmsCyclin DCyclin-Dependent Kinase 6Cyclin EEnzyme InhibitorsG1 PhaseGene Expression Regulation, NeoplasticHumansHydrolasesMicroRNAsProtein-Arginine DeiminasesProtein IsoformsSignal TransductionAmidinesCDK6 protein, humanCyclin DCyclin-Dependent Kinase 6Cyclin EEnzyme InhibitorsHydrolasesMicroRNAsMIRN16 microRNA, humanProtein-Arginine DeiminasesProtein IsoformsTumor Suppressor Protein p53

Identifiers

PMID23308284
PMCPMC3538596
OpenAlexW2048641238

What OpenQuestion holds

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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.