Evidence map›Paper›PMID 31649334›Full record

ArticleOncogene2020

Disruption of gap junctions attenuates acute myeloid leukemia chemoresistance induced by bone marrow mesenchymal stromal cells.

Farah Kouzi, Kazem Zibara, Jerome Bourgeais, Frederic Picou, Nathalie Gallay, Julie Brossaud, Hassan Dakik, Benjamin Roux, Sophie Hamard, Louis-Romee Le Nail and 12 more

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oncogene, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 46 citations in OpenAlex.

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  20. Regulation of Malignant Myeloid Leukemia by Mesenchymal Stem Cells.Frontiers in cell and developmental biology · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 5 institutions in 2 countries.

Farah KouziCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Kazem Zibara *PRASE, DSST, Lebanese University, Beirut, Lebanon.ORCID http://orcid.org/0000-0002-9887-072X
Jerome Bourgeais *CNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Frederic PicouCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Nathalie GallayCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Julie BrossaudDepartment of Nuclear Medicine, Bordeaux University Hospital, Pessac, France.
Hassan DakikCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.ORCID http://orcid.org/0000-0003-0270-8195
Benjamin RouxCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Sophie HamardCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Louis-Romee Le NailDepartment of Surgical Orthopedia, Tours University Hospital, Tours, France.
Rita HleihelDepartment of Anatomy, Cell Biology, and Physiological Sciences, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.
Amelie FoucaultCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Noemie RavaletCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Florence Rouleux-BonninCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Fabrice GouilleuxCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Frederic MazurierCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Marie C BeneDepartment of Biological Hematology, Nantes University Hospital, CRCINA, Nantes, France.
Haidar AklPRASE, DSST, Lebanese University, Beirut, Lebanon.
Emmanuel GyanCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Jorge DomenechCNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France.
Marwan El-Sabban *Department of Anatomy, Cell Biology, and Physiological Sciences, Faculty of Medicine, American University of Beirut, Beirut, Lebanon.
Olivier Herault *CNRS ERL7001 LNOx "Leukemic Niche & Redox Metabolism", Tours, France. olivier.herault@univ-tours.fr.ORCID http://orcid.org/0000-0002-7419-1124
Université de Tours · FRAmerican University of Beirut · LBLebanese University · LBNantes Université · FRUniversité de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The bone marrow (BM) niche impacts the progression of acute myeloid leukemia (AML) by favoring the chemoresistance of AML cells. Intimate interactions between leukemic cells and BM mesenchymal stromal cells (BM-MSCs) play key roles in this process. Direct intercellular communications between hematopoietic cells and BM-MSCs involve connexins, components of gap junctions. We postulated that blocking gap junction assembly could modify cell-cell interactions in the leukemic niche and consequently the chemoresistance. The comparison of BM-MSCs from AML patients and healthy donors revealed a specific profile of connexins in BM-MSCs of the leukemic niche and the effects of carbenoxolone (CBX), a gap junction disruptor, were evaluated on AML cells. CBX presents an antileukemic effect without affecting normal BM-CD34

Indexed as

Drug Resistance, NeoplasmAnimalsAntimetabolites, AntineoplasticAnti-Ulcer AgentsApoptosisCarbenoxoloneCell ProliferationCytarabineDrug Therapy, CombinationGap JunctionsHumansLeukemia, Myeloid, AcuteMesenchymal Stem CellsMiceMice, Inbred NODMice, SCIDAntimetabolites, AntineoplasticAnti-Ulcer AgentsCarbenoxoloneCytarabine

Identifiers

PMID31649334
PMCPMC7002301
OpenAlexW2982010247

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.