Evidence map›Paper›PMID 28241871›Full record

ArticleMolecular cancer2017

A loss of host-derived MMP-7 promotes myeloma growth and osteolytic bone disease in vivo.

S T Lwin, J A Fowler, M T Drake, J R Edwards, C C Lynch, C M Edwards

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 38% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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  9. New Therapeutic Options for Advanced Hepatocellular Carcinoma.Cancer control : journal of the Moffitt Cancer Center
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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

6 authors at 4 institutions in 2 countries.

S T LwinNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK.
J A FowlerDepartment of Medicine/Clinical Pharmacology, Vanderbilt Center for Bone Biology, Nashville, USA.
M T DrakeDivision of Endocrinology, Mayo Clinic College of Medicine, Rochester, MN, USA.
J R EdwardsNuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Botnar Research Centre, University of Oxford, Old Road, Oxford, OX3 7LD, UK.
C C LynchDepartment of Tumor Biology, H. Lee Moffitt Cancer Center, Tampa, FL, USA.
C M EdwardsNuffield Department of Surgical Sciences, University of Oxford, Oxford, UK. claire.edwards@ndorms.ox.ac.uk.
Nuffield Orthopaedic Centre · GBMayo Clinic · USMoffitt Cancer Center · USVanderbilt University · US

Funding

TISSUE BANK AND CLINICAL/LABORATORY DATABASEP01CA062242 · NCI · MAYO CLINIC ROCHESTER · PI THERNEAU, TERRY M · 1994 to 2009
$12.9M
Host MMP-mediated regulation of the vicious cycle of prostate to bone metastasesR01CA143094 · NCI · VANDERBILT UNIVERSITY · PI LYNCH, CONOR C · 2010 to 2014
$1.5M
Role of the Bone Marrow Microenvironment in the Development of Multiple MyelomaR01CA137116 · NCI · VANDERBILT UNIVERSITY · PI EDWARDS, CLAIRE · 2010 to 2015
$1.2M
NCI NIH HHS P01 CA062242NCI NIH HHS R01 CA137116NCI NIH HHS R01 CA143094
6 · The paper itself

Abstract

Matrix metalloproteinases (MMPs) play a critical role in cancer pathogenesis, including tumor growth and osteolysis within the bone marrow microenvironment. However, the anti-tumor effects of MMPs are poorly understood, yet have significant implications for the therapeutic potential of targeting MMPs. Host derived MMP-7 has previously been shown to support the growth of bone metastatic breast and prostate cancer. In contrast and underscoring the complexity of MMP biology, here we identified a tumor-suppressive role for host MMP-7 in the progression of multiple myeloma in vivo. An increase in tumor burden and osteolytic bone disease was observed in myeloma-bearing MMP-7 deficient mice, as compared to wild-type controls. We observed that systemic MMP-7 activity was reduced in tumor-bearing mice and, in patients with multiple myeloma this reduced activity was concomitant with increased levels of the endogenous MMP inhibitor, tissue inhibitor of metalloproteinases-1 (TIMP-1). Our studies have identified an unexpected tumour-suppressive role for host-derived MMP-7 in myeloma bone disease in vivo, and highlight the importance of elucidating the effect of individual MMPs in a disease-specific context.

Indexed as

AnimalsBone NeoplasmsCell Line, TumorCell SurvivalDisease ProgressionGene Knockout TechniquesHumansMatrix Metalloproteinase 7MiceMultiple MyelomaNeoplasm TransplantationTumor MicroenvironmentMatrix Metalloproteinase 7MMP7 protein, humanBoneBone diseaseMicroenvironmentMMP-7Mouse modelMultiple myelomaOsteoclast

Identifiers

PMID28241871
PMCPMC5330156
OpenAlexW2594213931

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.