Evidence map›Paper›PMID 24950307›Full record

ArticleStem cell research2014

Deletion of Ptp4a3 reduces clonogenicity and tumor-initiation ability of colitis-associated cancer cells in mice.

Julie M Cramer, Mark W Zimmerman, Tim Thompson, Gregg E Homanics, John S Lazo, Eric Lagasse

Open access · goldAbstract read
In one paragraph

Article in Stem cell research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. A chemical genetics approach identifies PTP4A3 as a regulator of colon cancer cell adhesion.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2018
    Article
  6. Article
  7. Article
  8. Article
  9. Molecular Pathways: Targeting Protein Tyrosine Phosphatases in Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2017
    Review
  10. Article
  11. Article
  12. 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

6 authors at 2 institutions in 1 country.

Julie M Cramer *Department of Pathology, 200 Lothrop Street, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15261.
Mark W Zimmerman *Department of Pharmacology and Chemical Biology, University of Pittsburgh, 203 Lothrop Street, Pittsburgh, PA, 15260.
Tim ThompsonDepartment of Bioengineering, 3700 O'Hara St, University of Pittsburgh, Pittsburgh, PA, 15261.
Gregg E HomanicsDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, 203 Lothrop Street, Pittsburgh, PA, 15260.
John S LazoDepartment of Pharmacology and Chemical Biology, University of Pittsburgh, 203 Lothrop Street, Pittsburgh, PA, 15260.
Eric LagasseDepartment of Pathology, 200 Lothrop Street, University of Pittsburgh School of Medicine, Pittsburgh, PA, 15261.
University of Pittsburgh · USMcGowan Institute for Regenerative Medicine · US

Funding

University of Pittsburgh Clinical and Translational Science InstituteUL1TR000005 · NCATS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI REIS, STEVEN E · 2012 to 2015
$50.8M
Ethanol Mechanisms in GABAAR Gene Targeted MiceR37AA010422 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOMANICS, GREGG E. · 2010 to 2019
$4.4M
Organogenesis of Ectopic Tissue in Lymph NodeR01DK085711 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LAGASSE, ERIC · 2009 to 2013
$3.6M
ETHANOL MECHANISMS IN GABAAR GENE TARGETED MICER01AA010422 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI HOMANICS, GREGG E. · 1995 to 2008
$3.1M
The Role of Phosphatase of Regenerating Liver-3 in Alcohol-Associated DiseaseF31AA019597 · NIAAA · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI ZIMMERMAN, MARK W. · 2011 to 2012
$84k
NCATS NIH HHS UL1 TR000005NIAAA NIH HHS AA10422NIAAA NIH HHS F31 AA019597NIAAA NIH HHS R01 AA010422NIAAA NIH HHS R37 AA010422NIDDK NIH HHS DK085711NIDDK NIH HHS R01 DK085711PHS HHS FAA019597
6 · The paper itself

Abstract

The PTP4A3 gene is highly expressed in human colon cancer and often associates with enhanced metastatic potential. Genetic disruption of the mouse Ptp4a3 gene reduces the frequency of colon tumor formation in mice treated in a colitis-associated cancer model. In the current study, we have examined the role of Ptp4a3 in the tumor-initiating cell population of mouse colon tumors using an in vitro culture system. Tumors generated in vivo following AOM/DSS treatment were isolated, dissociated, and expanded on a feeder layer resulting in a CD133(+) cell population, which expressed high levels of Ptp4a3. Tumor cells deficient for Ptp4a3 exhibited reduced clonogenicity and growth potential relative to WT cells as determined by limiting dilution analysis. Importantly, expanded tumor cells from WT mice readily formed secondary tumors when transplanted into nude mice, while tumor cells without Ptp4a3 expression failed to form secondary tumors and thus were not tumorigenic. These results demonstrate that Ptp4a3 contributes to the malignant phenotype of tumor-initiating cells and supports its role as a potential therapeutic target to inhibit tumor self-renewal and metastasis.

Indexed as

AnimalsColitisColonic NeoplasmsDisease Models, AnimalImmediate-Early ProteinsMiceMice, KnockoutNeoplastic Stem CellsProtein Tyrosine PhosphatasesImmediate-Early ProteinsProtein Tyrosine PhosphatasesPtp4a3 protein, mouse

Identifiers

PMID24950307
PMCPMC4090270
OpenAlexW2015008880

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.