Evidence map›Paper›PMID 37407572›Full record

ArticleCell death discovery2023

Galectin-9 has non-apoptotic cytotoxic activity toward acute myeloid leukemia independent of cytarabine resistance.

Ghizlane Choukrani, Nienke Visser, Natasha Ustyanovska Avtenyuk, Mirjam Olthuis, Glenn Marsman, Emanuele Ammatuna, Harm Jan Lourens, Toshiro Niki, Gerwin Huls, Edwin Bremer and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death discovery, 2023. 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
1.3field-weighted citation impact, top 19% 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, 8 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

11 authors at 2 institutions in 3 countries.

Ghizlane Choukrani *Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Nienke Visser *Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Natasha Ustyanovska AvtenyukDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Mirjam OlthuisDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Glenn MarsmanDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Emanuele AmmatunaDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Harm Jan LourensDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Toshiro NikiDepartment of Immunology, Kagawa University, Takamatsu, Kagawa, Japan.
Gerwin HulsDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Edwin BremerDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
Valerie R WiersmaDepartment of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands. v.wiersma@umcg.nl.ORCID http://orcid.org/0000-0001-8012-0376
University Medical Center Groningen · NLKagawa University · JP

Funding

EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 Marie Skłodowska-Curie Actions (H2020 Excellent Science - Marie Skłodowska-Curie Actions) No 813871KWF Kankerbestrijding (Dutch Cancer Society) KWF10709
6 · The paper itself

Abstract

Acute myeloid leukemia (AML) is a malignancy still associated with poor survival rates, among others, due to frequent occurrence of therapy-resistant relapse after standard-of-care treatment with cytarabine (AraC). AraC triggers apoptotic cell death, a type of cell death to which AML cells often become resistant. Therefore, therapeutic options that trigger an alternate type of cell death are of particular interest. We previously identified that the glycan-binding protein Galectin-9 (Gal-9) has tumor-selective and non-apoptotic cytotoxicity towards various types of cancer, which depended on autophagy inhibition. Thus, Gal-9 could be of therapeutic interest for (AraC-resistant) AML. In the current study, treatment with Gal-9 was cytotoxic for AML cells, including for CD34

Identifiers

PMID37407572
PMCPMC10322858
OpenAlexW4383302130

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.