Evidence map›Paper›PMID 25013764›Full record

ReviewBioMed research international2014

Immunological dysregulation in multiple myeloma microenvironment.

Alessandra Romano, Concetta Conticello, Maide Cavalli, Calogero Vetro, Alessia La Fauci, Nunziatina Laura Parrinello, Francesco Di Raimondo

Open access · hybridAbstract readReview
In one paragraph

Review in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 80 papers.

0numbers the graph read from it
0cells of the map it votes in
80citing papers in PubMed
8.7field-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

80 citing papers in PubMed, 123 citations in OpenAlex.

  1. Trial
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  9. Multiple myeloma and the potential of new checkpoint inhibitors for immunotherapy.Therapeutic advances in vaccines and immunotherapy · 2024
    Review
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  11. Article
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20 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

7 authors at 3 institutions in 1 country.

Alessandra RomanoDepartment of Clinical and Molecular Biomedicine, Haematology Section, University of Catania, Catania, Italy ; Fondazione Veronesi, Roma, Italy ; Division of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.
Concetta ConticelloDivision of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.
Maide CavalliDivision of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.ORCID 0000-0002-7339-5141
Calogero VetroDepartment of Clinical and Molecular Biomedicine, Haematology Section, University of Catania, Catania, Italy ; Division of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.ORCID 0000-0003-1922-5157
Alessia La FauciDivision of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.
Nunziatina Laura ParrinelloDepartment of Clinical and Molecular Biomedicine, Haematology Section, University of Catania, Catania, Italy ; Division of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.
Francesco Di RaimondoDepartment of Clinical and Molecular Biomedicine, Haematology Section, University of Catania, Catania, Italy ; Division of Hematology, AOU "Policlinico-Vittorio Emanuele", Catania, Italy.ORCID 0000-0002-7749-0293
Azienda Ospedaliero-Universitaria Policlinico - Vittorio Emanuele · ITUniversity of Catania · ITFondazione Roma · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple Myeloma (MM) is a systemic hematologic disease due to uncontrolled proliferation of monoclonal plasma cells (PC) in bone marrow (BM). Emerging in other solid and liquid cancers, the host immune system and the microenvironment have a pivotal role for PC growth, proliferation, survival, migration, and resistance to drugs and are responsible for some clinical manifestations of MM. In MM, microenvironment is represented by the cellular component of a normal bone marrow together with extracellular matrix proteins, adhesion molecules, cytokines, and growth factors produced by both stromal cells and PC themselves. All these components are able to protect PC from cytotoxic effect of chemo- and radiotherapy. This review is focused on the role of immunome to sustain MM progression, the emerging role of myeloid derived suppressor cells, and their potential clinical implications as novel therapeutic target.

Indexed as

CarcinogenesisMolecular Targeted TherapyBone Marrow CellsCell ProliferationDendritic CellsHumansMultiple MyelomaT-Lymphocytes, RegulatoryTumor Microenvironment

Identifiers

PMID25013764
PMCPMC4071780
OpenAlexW2046280953

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.