Evidence map›Paper›PMID 26155424›Full record

ArticleOncoimmunology2015

Modifications of the mouse bone marrow microenvironment favor angiogenesis and correlate with disease progression from asymptomatic to symptomatic multiple myeloma.

Arianna Calcinotto, Maurilio Ponzoni, Roberto Ria, Matteo Grioni, Elena Cattaneo, Isabella Villa, Maria Teresa Sabrina Bertilaccio, Marta Chesi, Alessandro Rubinacci, Giovanni Tonon and 3 more

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

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  16. Microbiota-Propelled T Helper 17 Cells in Inflammatory Diseases and Cancer.Microbiology and molecular biology reviews : MMBR · 2020
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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

13 authors at 5 institutions in 3 countries.

Arianna CalcinottoCellular Immunology Unit; IRCCS San Raffaele Scientific Institute ; Milan, Italy ; Università Vita-Salute San Raffaele ; Milan, Italy.
Maurilio PonzoniPathology and Myeloma Units; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Roberto RiaDepartment of Biomedical Sciences and Human Oncology; Internal Medicine and Clinical Oncology Unit; University of Bari Medical School ; Bari, Italy.
Matteo GrioniCellular Immunology Unit; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Elena CattaneoCellular Immunology Unit; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Isabella VillaBone Metabolic Unit; Division of Cardiovascular Science; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Maria Teresa Sabrina BertilaccioDivision of Molecular Oncology; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Marta ChesiComprehensive Cancer Center; Mayo Clinic Arizona ; Scottsdale, AZ, USA.
Alessandro RubinacciBone Metabolic Unit; Division of Cardiovascular Science; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Giovanni TononDivision of Molecular Oncology; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
P Leif BergsagelComprehensive Cancer Center; Mayo Clinic Arizona ; Scottsdale, AZ, USA.
Angelo VaccaDepartment of Biomedical Sciences and Human Oncology; Internal Medicine and Clinical Oncology Unit; University of Bari Medical School ; Bari, Italy.
Matteo BelloneCellular Immunology Unit; IRCCS San Raffaele Scientific Institute ; Milan, Italy.
Vita-Salute San Raffaele University · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITMayo Clinic Hospital · USUniversity of Bari Aldo Moro · ITIstituto di Ricovero e Cura a Carattere Scientifico San Raffaele

Funding

PQD2 Rational Combination of Standard Agents and Immunotherapy to Treat MyelomaR01CA190045 · NCI · MAYO CLINIC ARIZONA · PI CHESI, MARTA · 2014 to 2017
$1.4M
NCI NIH HHS R01 CA190045
6 · The paper itself

Abstract

While multiple myeloma (MM) is almost invariably preceded by asymptomatic monoclonal gammopathy of undetermined significance (MGUS) and/or smoldering MM (SMM), the alterations of the bone marrow (BM) microenvironment that establish progression to symptomatic disease are circumstantial. Here we show that in Vk*MYC mice harboring oncogene-driven plasma cell proliferative disorder, disease appearance associated with substantial modifications of the BM microenvironment, including a progressive accumulation of both CD8

Indexed as

angiogenesisBMb, BM biopsiesBM, bone marrowmacrophagesMGUS, monoclonal gammopathy of undetermined significanceMM, multiple myelomaM-spike, monoclonal (M) proteinmultiple myelomaMVD, microvessel densitySMM, smoldering multiple myelomasmoldering multiple myelomaTAMs, M2 tumor associated macrophagesT cellsTEMs, Tie2-expressing macrophages

Identifiers

PMID26155424
PMCPMC4485787
OpenAlexW1533959918

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.