Evidence map›Paper›PMID 29440639›Full record

ArticleBlood cancer journal2018

The small GTPase RhoU lays downstream of JAK/STAT signaling and mediates cell migration in multiple myeloma.

Sara Canovas Nunes, Martina Manzoni, Marco Pizzi, Elisa Mandato, Marilena Carrino, Laura Quotti Tubi, Renato Zambello, Fausto Adami, Andrea Visentin, Gregorio Barilà and 5 more

Open access · goldAbstract read
In one paragraph

Article in Blood cancer journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.8field-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

17 citing papers in PubMed, 21 citations in OpenAlex.

  1. Decoding Rho GTPase signalling networks in directed cell migration.Frontiers in cell and developmental biology · 2026
    Review
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  5. Genes · 2022
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  12. The DNA-helicase HELLS drives ALKCell death & disease · 2021
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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

15 authors at 2 institutions in 2 countries.

Sara Canovas NunesDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Martina ManzoniHematology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.ORCID http://orcid.org/0000-0003-0861-9951
Marco PizziSurgical Pathology and Cytopathology Unit, Department of Medicine - DIMED, University of Padova, Padova, Italy.
Elisa MandatoDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Marilena CarrinoDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Laura Quotti TubiDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Renato ZambelloDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Fausto AdamiDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Andrea VisentinDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0003-0271-7200
Gregorio BarilàDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Livio TrentinDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0002-7447-2946
Sabrina ManniDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Antonino NeriHematology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Gianpietro SemenzatoDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy.
Francesco PiazzaDepartment of Medicine, Division of Hematology, University of Padova, Padova, Italy. francesco.piazza@unipd.it.
University of Padua · ITUniversity of Milan · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple myeloma is a post-germinal center B-cell neoplasm, characterized by the proliferation of malignant bone marrow plasma cells, whose survival and proliferation is sustained by growth factors and cytokines present in the bone marrow microenvironment. Among them, IL-6 triggers the signal downstream of its receptor, leading to the activation of the JAK/STAT pathway. The atypical GTPase RhoU lays downstream of STAT3 transcription factor and could be responsible for mediating its effects on cytoskeleton dynamics. Here we demonstrate that RHOU is heterogeneously expressed in primary multiple myeloma cells and significantly modulated with disease progression. At the mRNA level, RHOU expression in myeloma patients correlated with the expression of STAT3 and its targets MIR21 and SOCS3. Also, IL-6 stimulation of human myeloma cell lines up-regulated RHOU through STAT3 activation. On the other hand, RhoU silencing led to a decrease in cell migration with the accumulation of actin stress fibers, together with a decrease in cyclin D2 expression and in cell cycle progression. Furthermore, we found that even though lenalidomide positively regulated RhoU expression leading to higher cell migration rates, it actually led to cell cycle arrest probably through a p21 dependent mechanism. Lenalidomide treatment in combination with RhoU silencing determined a loss of cytoskeletal organization inhibiting cell migration, and a further increase in the percentage of cells in a resting phase. These results unravel a role for RhoU not only in regulating the migratory features of malignant plasma cells, but also in controlling cell cycle progression.

Indexed as

Cell CycleCell MovementSignal TransductionCell Line, TumorHumansJanus KinasesMultiple MyelomaNeoplasm Proteinsrho GTP-Binding ProteinsSTAT3 Transcription FactorJanus KinasesNeoplasm Proteinsrho GTP-Binding ProteinsRHOU protein, humanSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID29440639
PMCPMC5811530
OpenAlexW2791672691

What OpenQuestion holds

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LicenceCC BY
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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.