Evidence map›Paper›PMID 31439679›Full record

ArticleHaematologica2020

Multi-parametric single cell evaluation defines distinct drug responses in healthy hematologic cells that are retained in corresponding malignant cell types.

Muntasir M Majumder, Aino-Maija Leppä, Monica Hellesøy, Paul Dowling, Alina Malyutina, Reidun Kopperud, Despina Bazou, Emma Andersson, Alun Parsons, Jing Tang and 7 more

Abstract read
In one paragraph

Article in Haematologica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
–field-weighted citation impact
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

15 citing papers in PubMed.

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  12. Annual review of cancer biology · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors.

Muntasir M MajumderInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland muntasir.mamun@helsinki.fi.
Aino-Maija LeppäInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Monica HellesøyHematology Section, Department of Internal Medicine, Haukeland University Hospital, Bergen, Norway.
Paul DowlingDepartment of Biology, National University of Ireland, Maynooth, Ireland.
Alina MalyutinaInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Reidun KopperudCentre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, Bergen, Norway.
Despina BazouDepartment of Hematology, Mater Misericordiae University Hospital, Dublin, Ireland.
Emma AnderssonDepartment of Clinical Chemistry and Hematology, University of Helsinki, Finland.
Alun ParsonsInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Jing TangInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Olli KallioniemiInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Satu MustjokiDepartment of Clinical Chemistry and Hematology, University of Helsinki, Finland.
Peter O'GormanDepartment of Hematology, Mater Misericordiae University Hospital, Dublin, Ireland.
Krister WennerbergInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland.
Kimmo PorkkaHematology Research Unit Helsinki, University of Helsinki, Helsinki, Finland.
Bjørn T GjertsenHematology Section, Department of Internal Medicine, Haukeland University Hospital, Bergen, Norway.
Caroline A HeckmanInstitute for Molecular Medicine Finland FIMM, Helsinki Institute of Life Science, University of Helsinki, Helsinki, Finland caroline.heckman@helsinki.fi.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Innate drug sensitivity in healthy cells aids identification of lineage specific anti-cancer therapies and reveals off-target effects. To characterize the diversity in drug responses in the major hematopoietic cell types, we simultaneously assessed their sensitivity to 71 small molecules utilizing a multi-parametric flow cytometry assay and mapped their proteomic and basal signaling profiles. Unsupervised hierarchical clustering identified distinct drug responses in healthy cell subsets based on their cellular lineage. Compared to other cell types, CD19

Indexed as

Leukemia, Lymphocytic, Chronic, B-CellLeukemia, Myeloid, AcutePharmaceutical PreparationsFlow CytometryHumansProteomicsPharmaceutical Preparations

Identifiers

PMID31439679
PMCPMC7271564

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.