Evidence map›Paper›PMID 29074954›Full record

ArticleScientific reports2017

Functional Activation of Osteoclast Commitment in Chronic Lymphocytic Leukaemia: a Possible Role for RANK/RANKL Pathway.

Cecilia Marini, Silvia Bruno, Francesco Fiz, Cristina Campi, Roberta Piva, Giovanna Cutrona, Serena Matis, Alberto Nieri, Maurizio Miglino, Adalberto Ibatici and 22 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

11 citing papers in PubMed, 19 citations in OpenAlex.

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  10. Metabolic and densitometric correlation between atherosclerotic plaque and trabecular bone: anAmerican journal of nuclear medicine and molecular imaging · 2018
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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

32 authors at 7 institutions in 3 countries.

Cecilia MariniCNR Institute of Bioimages and Molecular Physiology, Milan, Italy. Cecilia.marini@unige.it.
Silvia BrunoDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Francesco FizNuclear Medicine, Department of Health Science, University of Genova, Genoa, Italy.
Cristina CampiSPIN Institute, CNR, Genoa, Italy.
Roberta PivaNuclear Medicine, Department of Health Science, University of Genova, Genoa, Italy.
Giovanna CutronaMolecular Pathology, IRCCS AOU San Martino-IST, Genoa, Italy.ORCID 0000-0002-3335-1101
Serena MatisMolecular Pathology, IRCCS AOU San Martino-IST, Genoa, Italy.
Alberto NieriNuclear Medicine, Department of Health Science, University of Genova, Genoa, Italy.
Maurizio MiglinoDepartment of Internal Medicine, University of Genoa, Genoa, Italy.
Adalberto IbaticiHaematology Clinic, IRCCS AOU San Martino-IST, Genoa, Italy.
Anna Maria OrengoNuclear Medicine IRCCS AOU San Martino-IST, Genoa, Italy.
Anna Maria MassoneSPIN Institute, CNR, Genoa, Italy.
Carlo Emanuele NeumaierRadiology Unit, IRCCS AOU San Martino-IST, Genoa, Italy.
Daniela de ToteroTransfer Gene Laboratory, IRCCS AOU San Martino-IST, Genoa, Italy.
Paolo GiannoniStem Cell Laboratory, Department of Experimental Medicine, University of Genova, Genoa, Italy.
Matteo BaucknehtNuclear Medicine, Department of Health Science, University of Genova, Genoa, Italy.
Michele PennoneNuclear Medicine IRCCS AOU San Martino-IST, Genoa, Italy.
Claudya TencaDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Elena GugiattiDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Alessandro BelliniNuclear Medicine, Department of Health Science, University of Genova, Genoa, Italy.
Anna BorraNuclear Medicine, Department of Health Science, University of Genova, Genoa, Italy.
Elisabetta TedoneHaematology Clinic, IRCCS AOU San Martino-IST, Genoa, Italy.
Hülya EfetürkNuclear Medicine IRCCS AOU San Martino-IST, Genoa, Italy.
Francesca RosaRadiology Unit, IRCCS AOU San Martino-IST, Genoa, Italy.
Laura EmioniteAnimal Facility, IRCCS AOU San Martino-IST, Genoa, Italy.
Michele CilliAnimal Facility, IRCCS AOU San Martino-IST, Genoa, Italy.
Davide BagnaraDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Valerio BrucatoDepartment of Civil, Environmental, Aerospace, Materials Engineering, Aten Center, CHAB pole, University of Palermo, Viale delle Scienze, 6, Palermo, 90128, Italy.
Paolo BruzziEpidemiology and Clinical trial Service, IRCCS AOU San Martino-IST, Genoa, Italy.
Michele PianaSPIN Institute, CNR, Genoa, Italy.
Franco FaisDepartment of Experimental Medicine, University of Genoa, Genoa, Italy.
Gianmario SambucetiNuclear Medicine IRCCS AOU San Martino-IST, Genoa, Italy.ORCID 0000-0003-2979-6500
Ospedale Policlinico San Martino · ITUniversity of Genoa · ITSuperconducting and other Innovative Materials and Devices Institute · ITInstitute of Molecular Bioimaging and Physiology · ITNorthwell Health · USUniversitätsklinikum Tübingen · DEUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Skeletal erosion has been found to represent an independent prognostic indicator in patients with advanced stages of chronic lymphocytic leukaemia (CLL). Whether this phenomenon also occurs in early CLL phases and its underlying mechanisms have yet to be fully elucidated. In this study, we prospectively enrolled 36 consecutive treatment-naïve patients to analyse skeletal structure and bone marrow distribution using a computational approach to PET/CT images. This evaluation was combined with the analysis of RANK/RANKL loop activation in the leukemic clone, given recent reports on its role in CLL progression. Bone erosion was particularly evident in long bone shafts, progressively increased from Binet stage A to Binet stage C, and was correlated with both local expansion of metabolically active bone marrow documented by FDG uptake and with the number of RANKL + cells present in the circulating blood. In immune-deficient NOD/Shi-scid, γcnull (NSG) mice, administration of CLL cells caused an appreciable compact bone erosion that was prevented by Denosumab. CLL cell proliferation in vitro correlated with RANK expression and was impaired by Denosumab-mediated disruption of the RANK/RANKL loop. This study suggests an interaction between CLL cells and stromal elements able to simultaneously impair bone structure and increase proliferating potential of leukemic clone.

Indexed as

AdultAgedAged, 80 and overAnimalsBone Density Conservation AgentsBone MarrowDenosumabFemaleGlucoseHumansLeukemia, Lymphocytic, Chronic, B-CellMaleMice, Inbred NODMiddle AgedOsteoclastsPositron Emission Tomography Computed TomographyBone Density Conservation AgentsDenosumabGlucoseRANK LigandReceptor Activator of Nuclear Factor-kappa BTNFRSF11A protein, humanTNFSF11 protein, human

Identifiers

PMID29074954
PMCPMC5658396
OpenAlexW2765823369

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Registered trials

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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.