Evidence map›Paper›PMID 33202418›Full record

ArticleBlood2021

Hematoxylin binds to mutant calreticulin and disrupts its abnormal interaction with thrombopoietin receptor.

Ruochen Jia, Thomas Balligand, Vasyl Atamanyuk, Harini Nivarthi, Erica Xu, Leon Kutzner, Jakob Weinzierl, Audrey Nedelec, Stefan Kubicek, Roman Lesyk and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 9 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 4 institutions in 4 countries.

Ruochen JiaDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Thomas BalligandLudwig Cancer Research, de Duve Institute, Université Catholique de Louvain Brussels, Brussels, Belgium.
Vasyl AtamanyukDepartment of Pharmaceutical, Organic and Bioorganic Chemistry, Danylo Halytsky Lviv National Medical University, Lviv, Ukraine.
Harini NivarthiDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Erica XuMyeloPro Diagnostics and Research GmbH, Vienna, Austria.
Leon KutznerCeMM Research Center for Molecular Medicine, Austrian Academy of Sciences, Vienna, Austria.
Jakob WeinzierlDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Audrey NedelecLudwig Cancer Research, de Duve Institute, Université Catholique de Louvain Brussels, Brussels, Belgium.
Stefan KubicekCeMM Research Center for Molecular Medicine, Austrian Academy of Sciences, Vienna, Austria.
Roman LesykDepartment of Pharmaceutical, Organic and Bioorganic Chemistry, Danylo Halytsky Lviv National Medical University, Lviv, Ukraine.
Oleh ZagrijtschukPrivate Practice, Vienna, Austria.
Stefan N ConstantinescuLudwig Cancer Research, de Duve Institute, Université Catholique de Louvain Brussels, Brussels, Belgium.
Robert KralovicsDepartment of Laboratory Medicine, Medical University of Vienna, Vienna, Austria.
Austrian Academy of Sciences · ATLudwig Cancer Research · BEDanylo Halytsky Lviv National Medical University · UAMedical University of Vienna · AT

Funding

Austrian Science Fund FWF P 29018Austrian Science Fund FWF P 30041
6 · The paper itself

Abstract

Somatic mutations of calreticulin (CALR) have been identified as a main disease driver of myeloproliferative neoplasms, suggesting that development of drugs targeting mutant CALR is of great significance. Site-directed mutagenesis in the N-glycan binding domain (GBD) abolishes the ability of mutant CALR to oncogenically activate the thrombopoietin receptor (MPL). We therefore hypothesized that a small molecule targeting the GBD might inhibit the oncogenicity of the mutant CALR. Using an in silico molecular docking study, we identified candidate binders to the GBD of CALR. Further experimental validation of the hits identified a group of catechols inducing a selective growth inhibitory effect on cells that depend on oncogenic CALR for survival and proliferation. Apoptosis-inducing effects by the compound were significantly higher in the CALR-mutated cells than in CALR wild-type cells. Additionally, knockout or C-terminal truncation of CALR eliminated drug hypersensitivity in CALR-mutated cells. We experimentally confirmed the direct binding of the selected compound to CALR, disruption of the mutant CALR-MPL interaction, inhibition of the JAK2-STAT5 pathway, and reduction at the intracellular level of mutant CALR upon drug treatment. Our data indicate that small molecules targeting the GBD of CALR can selectively kill CALR-mutated cells by disrupting the CALR-MPL interaction and inhibiting oncogenic signaling.

Indexed as

AnimalsBinding SitesCalreticulinCell LineDrug DiscoveryHematoxylinHumansMiceMolecular Docking SimulationMutagenesis, Site-DirectedMutationMyeloproliferative DisordersProtein BindingProtein Interaction MapsReceptors, ThrombopoietinCalreticulinHematoxylinReceptors, Thrombopoietin

Identifiers

PMID33202418
PMCPMC8118640
OpenAlexW3099651974

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.