Evidence map›Paper›PMID 30286096›Full record

ArticlePloS one2018

Profiling of circulating exosomal miRNAs in patients with Waldenström Macroglobulinemia.

Juliette M Bouyssou, Chia-Jen Liu, Mark Bustoros, Romanos Sklavenitis-Pistofidis, Yosra Aljawai, Salomon Manier, Amir Yosef, Antonio Sacco, Katsutoshi Kokubun, Shokichi Tsukamoto and 9 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

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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

19 authors at 4 institutions in 3 countries.

Juliette M BouyssouDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.ORCID 0000-0002-2301-0426
Chia-Jen LiuDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.ORCID 0000-0001-7945-9292
Mark BustorosDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.ORCID 0000-0002-4652-5449
Romanos Sklavenitis-PistofidisDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Yosra AljawaiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Salomon ManierDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Amir YosefDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.ORCID 0000-0002-9322-1798
Antonio SaccoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Katsutoshi KokubunDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Shokichi TsukamotoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Adriana Perilla GlenDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Daisy HuynhDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.ORCID 0000-0002-4633-4570
Jorge J CastilloDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Steven P TreonDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Véronique LeblondDepartment of Hematology at Pitié Salpêtrière Hospital, Paris, France.
Olivier HermineINSERM UMR 1163, Laboratory of Cellular and Molecular Mechanisms of Hematological Disorders and Therapeutic Implications, Paris, France.
Aldo M RoccaroDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Irene M GhobrialDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Marzia CapellettiDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston MA, United States of America.
Harvard University · USHôpital Necker-Enfants Malades · FRInserm · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Waldenström Macroglobulinemia (WM) is a low-grade B-cell lymphoma characterized by disease progression from IgM MGUS to asymptomatic and then symptomatic disease states. We profiled exosomes from the peripheral blood of patients with WM at different stages (30 smoldering/asymptomatic WM, 44 symptomatic WM samples and 10 healthy controls) to define their role as potential biomarkers of disease progression. In this study, we showed that circulating exosomes and their miRNA content represent unique markers of the tumor and its microenvironment. We observed similar levels of miRNAs in exosomes from patients with asymptomatic (smoldering) and symptomatic WM, suggesting that environmental and clonal changes occur in patients at early stages of disease progression before symptoms occur. Moreover, we identified a small group of miRNAs whose expression correlated directly or inversely with the disease status of patients, notably the known tumor suppressor miRNAs let-7d and the oncogene miR-21 as well as miR-192 and miR-320b. The study of these miRNAs' specific effect in WM cells could help us gain further insights on the mechanisms underlying WM pathogenesis and reveal their potential as novel therapeutic targets for this disease.

Indexed as

AdultAgedBiomarkersCell LineDisease ProgressionExosomesFemaleGene Expression Regulation, NeoplasticHumansMaleMicroRNAsMiddle AgedWaldenstrom MacroglobulinemiaBiomarkersMicroRNAs

Identifiers

PMID30286096
PMCPMC6171840
OpenAlexW2895221165

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.