Evidence map›Paper›PMID 25061176›Full record

Trial reportBlood2014

The sialyltransferase ST3GAL6 influences homing and survival in multiple myeloma.

Siobhan V Glavey, Salomon Manier, Alessandro Natoni, Antonio Sacco, Michele Moschetta, Michaela R Reagan, Laura S Murillo, Ilyas Sahin, Ping Wu, Yuji Mishima and 8 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

84 citing papers in PubMed, 132 citations in OpenAlex.

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  15. Cancers · 2024
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24 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

18 authors at 5 institutions in 3 countries.

Siobhan V GlaveyDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA; Department of Hematology, National University of Ireland, Galway and Galway University Hospital, Galway, Ireland;
Salomon ManierDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Alessandro NatoniDepartment of Hematology, National University of Ireland, Galway and Galway University Hospital, Galway, Ireland;
Antonio SaccoDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Michele MoschettaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Michaela R ReaganDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Laura S MurilloDepartment of Hematology, National University of Ireland, Galway and Galway University Hospital, Galway, Ireland;
Ilyas SahinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Ping WuCentre for Myeloma Research, Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom; and.
Yuji MishimaDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Yu ZhangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Wenjing ZhangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Yong ZhangDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Gareth MorganCentre for Myeloma Research, Division of Molecular Pathology, The Institute of Cancer Research, London, United Kingdom; and.
Lokesh JoshiGlycoscience Research Group, National University of Ireland, Galway, Ireland.
Aldo M RoccaroDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Irene M GhobrialDepartment of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA;
Michael E O'DwyerDepartment of Hematology, National University of Ireland, Galway and Galway University Hospital, Galway, Ireland; Glycoscience Research Group, National University of Ireland, Galway, Ireland.
Dana-Farber Cancer Institute · USHarvard University · USInstitute of Cancer Research · GBOllscoil na Gaillimhe – University of Galway · IEUniversity Hospital Galway · IE

Funding

The role of miRNA15a and 16-1 in Multiple MyelomaR01CA154648 · NCI · DANA-FARBER CANCER INST · PI GHOBRIAL, IRENE M. · 2011 to 2015
$1.8M
NCI NIH HHS R01 CA154648
6 · The paper itself

Abstract

Glycosylation is a stepwise procedure of covalent attachment of oligosaccharide chains to proteins or lipids, and alterations in this process, especially increased sialylation, have been associated with malignant transformation and metastasis. The role of altered sialylation in multiple myeloma (MM) cell trafficking has not been previously investigated. In the present study we identified high expression of β-galactoside α-2,3-sialyltransferase, ST3GAL6, in MM cell lines and patients. This gene plays a key role in selectin ligand synthesis in humans through the generation of functional sialyl Lewis X. In MRC IX patients, high expression of this gene is associated with inferior overall survival. In this study we demonstrate that knockdown of ST3GAL6 results in a significant reduction in levels of α-2,3-linked sialic acid on the surface of MM cells with an associated significant reduction in adhesion to MM bone marrow stromal cells and fibronectin along with reduced transendothelial migration in vitro. In support of our in vitro findings, we demonstrate significantly reduced homing and engraftment of ST3GAL6 knockdown MM cells to the bone marrow niche in vivo, along with decreased tumor burden and prolonged survival. This study points to the importance of altered glycosylation, particularly sialylation, in MM cell adhesion and migration.

Indexed as

Transendothelial and Transepithelial MigrationAnimalsbeta-Galactoside alpha-2,3-SialyltransferaseBone Marrow CellsCell AdhesionCell Line, TumorCell SurvivalFemaleGene Knockdown TechniquesHumansHuman Umbilical Vein Endothelial CellsMaleMiceMice, SCIDMultiple MyelomaN-Acetylneuraminic Acidbeta-Galactoside alpha-2,3-SialyltransferaseN-Acetylneuraminic AcidNeoplasm ProteinsSialyltransferases

Identifiers

PMID25061176
PMCPMC4162107
OpenAlexW2141906566

What OpenQuestion holds

Textmetadata
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.