Evidence map›Paper›PMID 34728569›Full record

ArticleMolecular cancer therapeutics2022

Anti-apoptotic MCL1 Protein Represents Critical Survival Molecule for Most Burkitt Lymphomas and BCL2-negative Diffuse Large B-cell Lymphomas.

Magdalena Klanova, Dmitry Kazantsev, Eva Pokorna, Tomas Zikmund, Jana Karolova, Matej Behounek, Nicol Renesova, Dana Sovilj, Cristina D Kelemen, Karel Helman and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

15 authors at 3 institutions in 2 countries.

Magdalena Klanova *Institute of Pathological Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Dmitry Kazantsev *BIOCEV, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Eva PokornaInstitute of Pathological Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Tomas ZikmundBIOCEV, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0003-2452-3749
Jana KarolovaInstitute of Pathological Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0003-3828-6000
Matej BehounekBIOCEV, First Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID 0000-0002-6078-6653
Nicol RenesovaInstitute of Pathological Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic.
Dana SoviljInstitute of Biotechnology CAS/BIOCEV, Vestec, Czech Republic.
Cristina D KelemenInstitute of Biotechnology CAS/BIOCEV, Vestec, Czech Republic.
Karel HelmanPrague University of Economics and Business, Prague, Czech Republic.ORCID 0000-0001-7141-8074
Radek JaksaInstitute of Pathology, Charles University General Hospital, Prague, Czech Republic.ORCID 0000-0003-3910-4707
Ondrej HavranekFirst Department of Medicine-Department of Hematology, Charles University General Hospital, Prague, Czech Republic.
Ladislav AnderaInstitute of Biotechnology CAS/BIOCEV, Vestec, Czech Republic.
Marek TrnenyFirst Department of Medicine-Department of Hematology, Charles University General Hospital, Prague, Czech Republic.
Pavel KlenerInstitute of Pathological Physiology, First Faculty of Medicine, Charles University, Prague, Czech Republic. pavel.klener2@vfn.cz.ORCID 0000-0001-7786-9378
Charles University · CZCzech Academy of Sciences, Institute of Biotechnology · CZPrague University of Economics and Business · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The pro-survival MCL1 protein is overexpressed in many cancers, including B-cell non-Hodgkin lymphomas (B-NHL). S63845 is a highly specific inhibitor of MCL1. We analyzed mechanisms of sensitivity/resistance to S63845 in preclinical models of diffuse large B-cell lymphoma (DLBCL) and Burkitt lymphoma. Annexin V-based cytotoxic assays, Western blot analysis, protein co-immunoprecipitation, and cell clones with manipulated expression of BCL2 family proteins were used to analyze mechanisms of sensitivity to S63845. Experimental

Indexed as

ApoptosisBurkitt LymphomaCell Line, TumorHumansLymphoma, Large B-Cell, DiffuseMyeloid Cell Leukemia Sequence 1 ProteinProto-Oncogene Proteins c-bcl-2BCL2 protein, humanMCL1 protein, humanMyeloid Cell Leukemia Sequence 1 ProteinProto-Oncogene Proteins c-bcl-2

Identifiers

PMID34728569
PMCPMC9398137
OpenAlexW3208758994

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.