Evidence map›Paper›PMID 31068926›Full record

ReviewFrontiers in immunology2019

CD38 in Adenosinergic Pathways and Metabolic Re-programming in Human Multiple Myeloma Cells: In-tandem Insights From Basic Science to Therapy.

Alberto L Horenstein, Cristiano Bracci, Fabio Morandi, Fabio Malavasi

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 66 citations in OpenAlex.

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  18. Multiple myeloma and the potential of new checkpoint inhibitors for immunotherapy.Therapeutic advances in vaccines and immunotherapy · 2024
    Review
  19. A Population of Tumor-Infiltrating CD4+ T Cells Co-Expressing CD38 and CD39 Is Associated with Checkpoint Inhibitor Resistance.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
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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.

Alberto L HorensteinLaboratory of Immunogenetics, Department of Medical Sciences, Turin, Italy.
Cristiano BracciLaboratory of Immunogenetics, Department of Medical Sciences, Turin, Italy.
Fabio MorandiStem Cell Laboratory and Cell Therapy Center, Istituto Giannina Gaslini, Genova, Italy.
Fabio MalavasiLaboratory of Immunogenetics, Department of Medical Sciences, Turin, Italy.
University of Turin · ITIstituto Giannina Gaslini · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor microenvironments are rich in extracellular nucleotides that can be metabolized by ectoenzymes to produce adenosine, a nucleoside involved in controlling immune responses. Multiple myeloma, a plasma cell malignancy developed within a bone marrow niche, exploits adenosinergic pathways to customize the immune homeostasis of the tumor. CD38, a multifunctional protein that acts as both receptor and ectoenzyme, is overexpressed at all stages of myeloma. At neutral and acidic pH, CD38 catalyzes the extracellular conversion of NAD

Indexed as

Energy MetabolismSignal TransductionAdenosineADP-ribosyl Cyclase 1AnimalsAntineoplastic Agents, ImmunologicalDisease ManagementDisease ProgressionDisease SusceptibilityDrug Resistance, NeoplasmHumansImmunomodulationMembrane GlycoproteinsMetabolic Networks and PathwaysMolecular Targeted TherapyMultiple MyelomaAdenosineADP-ribosyl Cyclase 1Antineoplastic Agents, ImmunologicalCD38 protein, humanMembrane GlycoproteinsReceptors, PurinergicadenosineCD38immunotherapymetabolic reprogrammingmultiple myeloma

Identifiers

PMID31068926
PMCPMC6491463
OpenAlexW2940573123

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.