Evidence map›Paper›PMID 26967055›Full record

ArticleOncotarget2016

Notch signalling drives bone marrow stromal cell-mediated chemoresistance in acute myeloid leukemia.

Paul Takam Kamga, Giulio Bassi, Adriana Cassaro, Martina Midolo, Mariano Di Trapani, Alessandro Gatti, Roberta Carusone, Federica Resci, Omar Perbellini, Michele Gottardi and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
4.5field-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

61 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
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  6. Review
  7. Leukemic Stem Cells and Hematological Malignancies.International journal of molecular sciences · 2024
    Review
  8. Article
  9. Article
  10. Biology and Therapeutic Properties of Mesenchymal Stem Cells in Leukemia.International journal of molecular sciences · 2024
    Review
  11. Review
  12. Study Deciphering the Crucial Involvement of Notch Signaling Pathway in Human Cancers.Endocrine, metabolic & immune disorders drug targets · 2024
    Review
  13. Uncovering NOTCH1 as a Promising Target in the Treatment ofInternational journal of molecular sciences · 2023
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

1 more citing papers are in PubMed but not listed here.

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

14 authors at 3 institutions in 2 countries.

Paul Takam KamgaStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Giulio BassiStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Adriana CassaroStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Martina MidoloStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Mariano Di TrapaniStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Alessandro GattiStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Roberta CarusoneStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Federica ResciStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Omar PerbelliniStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Michele GottardiDivision of Hematology, Ca' Foncello Hospital, Treviso, Italy.
Massimiliano BonifacioStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Armel Hervé Nwabo KamdjeDepartment of Biomedical Sciences, University of Ngaoundere-Cameroon, Cameroon.
Achille AmbrosettiStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
Mauro KramperaStem Cell Research Laboratory, Section of Hematology, Department of Medicine, University of Verona, Verona, Italy.
University of Verona · ITCa' Foncello Hospital · ITUniversity of Ngaoundéré · CM

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Both preclinical and clinical investigations suggest that Notch signalling is critical for the development of many cancers and for their response to chemotherapy. We previously showed that Notch inhibition abrogates stromal-induced chemoresistance in lymphoid neoplasms. However, the role of Notch in acute myeloid leukemia (AML) and its contribution to the crosstalk between leukemia cells and bone marrow stromal cells remain controversial. Thus, we evaluated the role of the Notch pathway in the proliferation, survival and chemoresistance of AML cells in co-culture with bone marrow mesenchymal stromal cells expanded from both healthy donors (hBM-MSCs) and AML patients (hBM-MSCs*). As compared to hBM-MSCs, hBM-MSCs* showed higher level of Notch1, Jagged1 as well as the main Notch target gene HES1. Notably, hBM-MSCs* induced expression and activation of Notch signalling in AML cells, supporting AML proliferation and being more efficientin inducing AML chemoresistance than hBM-MSCs*. Pharmacological inhibition of Notch using combinations of Notch receptor-blocking antibodies or gamma-secretase inhibitors (GSIs), in presence of chemotherapeutic agents, significant lowered the supportive effect of hBM-MSCs and hBM-MSCs* towards AML cells, by activating apoptotic cascade and reducing protein level of STAT3, AKT and NF-κB.These results suggest that Notch signalling inhibition, by overcoming the stromal-mediated promotion of chemoresistance,may represent a potential therapeutic targetnot only for lymphoid neoplasms, but also for AML.

Indexed as

Signal TransductionAcute DiseaseAdultAgedBone Marrow CellsCell DifferentiationCell Line, TumorCells, CulturedCoculture TechniquesDrug Resistance, NeoplasmFemaleHL-60 CellsHumansK562 CellsLeukemia, MyeloidMalebenzyloxycarbonyl-leucyl-leucyl-norleucinalOligopeptidesReceptors, NotchAMLchemoresistanceMSCNotch

Identifiers

PMID26967055
PMCPMC5008317
OpenAlexW2340611212

What OpenQuestion holds

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LicenceCC BY
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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.