Evidence map›Paper›PMID 22019628›Full record

ArticleExperimental hematology2012

A46, a benzothiophene-derived compound, suppresses Jak2-mediated pathologic cell growth.

Anurima Majumder, Andrew T Magis, Sung O Park, Nicholas C Figueroa, Rebekah Baskin, Annet Kirabo, Robert W Allan, Zhizhuang Joe Zhao, Kirpal S Bisht, György M Keseru and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Experimental hematology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 91% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

11 authors at 6 institutions in 3 countries.

Anurima MajumderDepartment of Physiology and Functional Genomics, University of Florida College of Medicine, Gainesville, FL 32610, USA.
Andrew T Magis
Sung O Park
Nicholas C Figueroa
Rebekah Baskin
Annet Kirabo
Robert W Allan
Zhizhuang Joe Zhao
Kirpal S Bisht
György M Keseru
Peter P Sayeski
University of Florida · USFlorida College · USBudapest University of Technology and Economics · HUUniversity of Illinois Urbana-Champaign · USUniversity of Oklahoma Health Sciences Center · USUniversity of South Florida · US

Funding

UF Clinical and Translational Science AwardUL1TR000064 · NCATS · UNIVERSITY OF FLORIDA · PI NELSON, DAVID R · 2012 to 2014
$12.2M
The Role of Jak2 in Angiotensin II SignalingR01HL067277 · NHLBI · UNIVERSITY OF FLORIDA · PI SAYESKI, PETER P · 2002 to 2011
$2.9M
NCATS NIH HHS UL1 TR000064NHLBI NIH HHS R01 HL067277NHLBI NIH HHS R01-HL67277
6 · The paper itself

Abstract

Hyperkinetic Jak2 tyrosine kinase signaling has been implicated in several hematological disorders, including myeloproliferative neoplasms. Effective Jak2 inhibitors can have significant therapeutic potential. Here, using structure-based virtual screening, we identified a benzothiophene-derived Jak2 inhibitor named A46. We hypothesized that this compound would inhibit Jak2-V617F-mediated pathologic cell growth. To test this, A46 was analyzed for its ability to inhibit recombinant Jak2 protein catalysis; suppress Jak2-mediated pathogenic cell growth in vitro; inhibit the aberrant ex vivo growth of Jak2-V617F-expressing primary human bone marrow cells; and inhibit Jak2-mediated pathogenesis in vivo. To this end, we found that A46 selectively inhibited Jak2-V617F protein when compared to wild-type Jak2 protein. The drug also selectively inhibited the proliferation of Jak2-V617F-expressing cells in both a time- and dose-dependent manner, and this correlated with decreased Jak2 and signal transducers and activators of transcription 5 phosphorylation within treated cells. The Jak2-V617F cell growth inhibition correlated with an induction of cell cycle arrest and promotion of apoptosis. A46 also inhibited the pathologic growth of primary Jak2-V617F-expressing bone marrow cells ex vivo. Lastly, using a mouse model of Jak2-V617F-mediated myeloproliferative neoplasia. A46 significantly reduced the splenomegaly and megakaryocytic hyperplasia in the spleens of treated mice and the levels of interleukin-6 in the plasma. Collectively, our data demonstrate that the benzothiophene-based compound, A46, suppresses Jak2-mediated pathogenesis, thereby making it a potential candidate drug against Jak2-mediated disorders.

Indexed as

AnimalsApoptosisBiocatalysisBone Marrow CellsCell CycleCell ProliferationDose-Response Relationship, DrugHumansJanus Kinase 2MiceMice, TransgenicStructure-Activity RelationshipThiophenesTumor Cells, Cultured1-benzothiophen-2-yl-(4-dimethylaminophenyl)methanolJAK2 protein, humanJanus Kinase 2Thiophenes

Identifiers

PMID22019628
PMCPMC3237899
OpenAlexW2018794561

What OpenQuestion holds

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Registered trials

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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.