Evidence map›Paper›PMID 33540760›Full record

ArticleCancers2021

BMI1-Inhibitor PTC596 in Combination with MCL1 Inhibitor S63845 or MEK Inhibitor Trametinib in the Treatment of Acute Leukemia.

Katja Seipel, Basil Kopp, Ulrike Bacher, Thomas Pabst

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

12 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
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  10. BH3-mimetics: recent developments in cancer therapy.Journal of experimental & clinical cancer research : CR · 2021
    Review
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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

4 authors at 2 institutions in 1 country.

Katja SeipelDepartment for Biomedical Research (DBMR), University of Berne, 3008 Bern, Switzerland.ORCID 0000-0003-3128-1573
Basil KoppDepartment for Biomedical Research (DBMR), University of Berne, 3008 Bern, Switzerland.ORCID 0000-0002-8406-4436
Ulrike BacherDepartment of Hematology, University Hospital Berne, 3010 Bern, Switzerland.ORCID 0000-0001-8771-947X
Thomas PabstDepartment of Medical Oncology, University Hospital Berne, 3010 Bern, Switzerland.
University Hospital of Bern · CHUniversity of Bern · CH

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 310030_127509
6 · The paper itself

Abstract

purposePrognosis for acute myeloid leukemia (AML) patients is poor, particularly in EXPERIMENTAL

designThe BMI1 inhibitor PTC596, MCL1 inhibitor S63845, and MEK inhibitor trametinib, as well as the p53 activator APR-246 were assessed as single agents and in combination for their ability to induce apoptosis and cell death in leukemic cells. AML cells represented all major morphologic and molecular subtypes including

resultsAML cell lines were variably susceptible to PTC596 and to combination treatments with PTC596 and MCL1 inhibitor S63845, MEK inhibitor trametinib, or

conclusionsThe combination of PTC596 and S63845 may be an effective treatment in CD34+ adverse risk AML with elevated

Indexed as

acute myeloid leukemia (AML)B-cell-specific Moloney murine leukemia virus integration site 1 (BMI1)hematopoietic progenitor cell antigen cluster of differentiation 34 (CD34)meningioma 1 (MN1)myelodysplastic syndrome (MDS)myeloid cell leukemia 1 (MCL1)tumor suppressor protein 53 (TP53)

Identifiers

PMID33540760
PMCPMC7867282
OpenAlexW3127762095

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.