Evidence map›Paper›PMID 22001392›Full record

ArticleBlood2011

AP-1 elements and TCL1 protein regulate expression of the gene encoding protein tyrosine phosphatase PTPROt in leukemia.

Tasneem Motiwala, Nicola Zanesi, Jharna Datta, Satavisha Roy, Huban Kutay, Allyn M Checovich, Mohamed Kaou, Yiming Zhong, Amy J Johnson, David M Lucas and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
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  4. Observational
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  6. Article
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  12. Entering the era of targeted therapy for chronic lymphocytic leukemia: impact on the practicing clinician.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2014
    Review
  13. 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

17 authors at 1 institution in 1 country.

Tasneem MotiwalaDepartment of Molecular and Cellular Biochemistry, College of Medicine, The Ohio State University, Columbus, OH, USA. tasneem.motiwala@osumc.edu
Nicola Zanesi
Jharna Datta
Satavisha Roy
Huban Kutay
Allyn M Checovich
Mohamed Kaou
Yiming Zhong
Amy J Johnson
David M Lucas
Nyla A Heerema
John Hagan
Xiaokui Mo
David Jarjoura
John C Byrd
Carlo M Croce
Samson T Jacob
The Ohio State University · US

Funding

Translational Training Grant in Experimental TherapeuticsK12CA133250 · NCI · OHIO STATE UNIVERSITY · PI WILLIAM E. CARSON, Rosa Lapalombella · 2008 to 2026
$15.0M
PathologyP01CA101956 · NCI · OHIO STATE UNIVERSITY · PI FARAG, SHERIF S · 2006 to 2010
$11.4M
SPORE Leukemia Tissue BankP50CA140158 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D · 2009 to 2013
$11.2M
MOLECULAR MECHANISMS OF DIET-INDUCED CARCINOGENESISR01CA086978 · NCI · OHIO STATE UNIVERSITY · PI GHOSHAL, KALPANA, JACOB, SAMSON T · 2002 to 2018
$4.9M
TOWARD AN UNDERSTANDING OF CLL PROGRESSIONR01CA151319 · NCI · OHIO STATE UNIVERSITY · PI CROCE, CARLO M · 2011 to 2015
$1.5M
NCI NIH HHS 1K12 CA133250NCI NIH HHS CA101956NCI NIH HHS CA86978NCI NIH HHS K12 CA133250NCI NIH HHS P01 CA101956NCI NIH HHS P50 CA140158NCI NIH HHS R01 CA086978NCI NIH HHS R01 CA151319
6 · The paper itself

Abstract

We previously demonstrated that the gene encoding PTPROt, the truncated form of protein tyrosine phosphatase receptor type O expressed predominantly in hematopoietic cells, is a candidate tumor suppressor and is down-regulated in chronic lymphocytic leukemia (CLL). Here, we show that PTPROt expression is significantly reduced in CD19(+) spleen B cells from Eμ-T cell leukemia 1 (TCL1) transgenic mice relative to the wild-type mice. Strikingly, as much as a 60% decrease in PTPROt expression occurs at 7 weeks independently of promoter methylation. To elucidate the potential mechanism for this early suppression of PTPROt in these mice, we explored the role of activating protein-1 (AP-1) in its expression. We first demonstrate that AP-1 activation by 12-O-tetradecanoylphorbol-13-acetate induces PTPROt expression with concurrent recruitment of c-fos and c-jun to its promoter. The PTPROt promoter is also responsive to over- and underexpression of AP-1, confirming the role of AP-1 in PTPROt expression. Next, we demonstrate that TCL1 can repress the PTPROt promoter by altering c-fos expression and c-jun activation state. Finally, using primary CLL cells we have shown an inverse relationship between TCL1 and PTPROt expression. These findings further substantiate the role of TCL1 in PTPROt suppression and its importance in the pathogenesis of CLL.

Indexed as

AnimalsDisease Models, AnimalDown-RegulationGene Expression Regulation, LeukemicHumansK562 CellsLeukemia, B-CellLeukemia, Lymphocytic, Chronic, B-CellMiceMice, Inbred C3HMice, TransgenicPhosphorylationPromoter Regions, GeneticProto-Oncogene ProteinsProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-junProto-Oncogene ProteinsProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-junPTPRO protein, humanPtpro protein, mouseReceptor-Like Protein Tyrosine Phosphatases, Class 3TCL1A protein, humanTcl1 protein, mouseTranscription Factor AP-1

Identifiers

PMID22001392
PMCPMC3234669
OpenAlexW1999198691

What OpenQuestion holds

Textmetadata
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.