Evidence map›Paper›PMID 22094461›Full record

ArticleThe Journal of biological chemistry2012

Phospholipase D2 (PLD2) shortens the time required for myeloid leukemic cell differentiation: mechanism of action.

Mauricio Di Fulvio, Kathleen Frondorf, Karen M Henkels, William C Grunwald, David Cool, Julian Gomez-Cambronero

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 9 citations in OpenAlex.

  1. 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 1 institution in 1 country.

Mauricio Di FulvioDepartment of Biochemistry and Molecular Biology, Wright State University School Medicine, Dayton, Ohio, 45435.
Kathleen FrondorfDepartment of Biochemistry and Molecular Biology, Wright State University School Medicine, Dayton, Ohio, 45435.
Karen M HenkelsDepartment of Biochemistry and Molecular Biology, Wright State University School Medicine, Dayton, Ohio, 45435.
William C GrunwaldDepartment of Pharmacology and Toxicology, Wright State University School Medicine, Dayton, Ohio 45435.
David CoolDepartment of Pharmacology and Toxicology, Wright State University School Medicine, Dayton, Ohio 45435.
Julian Gomez-CambroneroDepartment of Biochemistry and Molecular Biology, Wright State University School Medicine, Dayton, Ohio, 45435. Electronic address: julian.cambronero@wright.edu.
Wright State University · US

Funding

PLD2, as a GEF or as a Lipase, is Central to Leukocyte ChemotaxisR01HL056653 · NHLBI · WRIGHT STATE UNIVERSITY · PI CAMBRONERO, JULIAN G. · 2004 to 2016
$4.0M
SIGNAL TRANSDUCTION IN NEUTROPHIL MEDIATED HEART INJURYR29HL056653 · NHLBI · WRIGHT STATE UNIVERSITY · PI GOMEZ-CAMBRONERO, JULIAN · 1998 to 2002
$301k
NHLBI NIH HHS HL056653NHLBI NIH HHS R01 HL056653NHLBI NIH HHS R29 HL056653
6 · The paper itself

Abstract

Cell differentiation is compromised in acute leukemias. We report that mammalian target of rapamycin (mTOR) and S6 kinase (S6K) are highly expressed in the undifferentiated promyelomonocytic leukemic HL-60 cell line, whereas PLD2 expression is minimal. The expression ratio of PLD2 to mTOR (or to S6K) is gradually inverted upon in vitro induction of differentiation toward the neutrophilic phenotype. We present three ways that profoundly affect the kinetics of differentiation as follows: (i) simultaneous overexpression of mTOR (or S6K), (ii) silencing of mTOR via dsRNA-mediated interference or inhibition with rapamycin, and (iii) PLD2 overexpression. The last two methods shortened the time required for differentiation. By determining how PLD2 participates in cell differentiation, we found that PLD2 interacts with and activates the oncogene Fes/Fps, a protein-tyrosine kinase known to be involved in myeloid cell development. Fes activity is elevated with PLD2 overexpression, phosphatidic acid or phosphatidylinositol bisphosphate. Co-immunoprecipitation indicates a close PLD2-Fes physical interaction that is negated by a Fes-R483K mutant that incapacitates its Src homology 2 domain. All these suggest for the first time the following mechanism: mTOR/S6K down-regulation→PLD2 overexpression→PLD2/Fes association→phosphatidic acid-led activation of Fes kinase→granulocytic differentiation. Differentiation shortening could have a clinical impact on reducing the time of return to normalcy of the white cell counts after chemotherapy in patients with acute promyelocytic leukemia.

Indexed as

Cell DifferentiationBase SequenceEnzyme ActivationGene SilencingHL-60 CellsHumansKineticsLeukemia, MyeloidMolecular Sequence DataPhospholipase DProto-Oncogene Proteins c-fesRibosomal Protein S6 KinasesRNA, Messengersrc Homology DomainsTOR Serine-Threonine KinasesUp-RegulationFES protein, humanPhospholipase Dphospholipase D2Proto-Oncogene Proteins c-fesRibosomal Protein S6 KinasesRNA, MessengerTOR Serine-Threonine Kinases

Identifiers

PMID22094461
PMCPMC3249091
OpenAlexW2018714786

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.