Evidence map›Paper›PMID 33526510›Full record

ArticleCancer research2021

Host-Derived Matrix Metalloproteinase-13 Activity Promotes Multiple Myeloma-Induced Osteolysis and Reduces Overall Survival.

Chen Hao Lo, Gemma Shay, Jeremy J McGuire, Tao Li, Kenneth H Shain, Jun Yong Choi, Rita Fuerst, William R Roush, Anna M Knapinska, Gregg B Fields and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

12 citing papers in PubMed, 18 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

11 authors at 6 institutions in 2 countries.

Chen Hao Lo *Department of Tumor Biology, University of South Florida, Tampa, Florida.ORCID 0000-0001-8848-2507
Gemma Shay *Department of Tumor Biology, University of South Florida, Tampa, Florida.
Jeremy J McGuireDepartment of Tumor Biology, University of South Florida, Tampa, Florida.
Tao LiDepartment of Tumor Biology, University of South Florida, Tampa, Florida.
Kenneth H ShainMalignant Hematology, H. Lee Moffitt Cancer Center, Tampa, Florida.
Jun Yong ChoiDepartment of Chemistry and Biochemistry Queens College, Queens, New York.ORCID 0000-0001-8218-6440
Rita FuerstDepartment of Organic Chemistry, Graz University of Technology, Graz, Austria.
William R RoushDepartment of Chemistry, Scripps Research Institute, Jupiter, Florida.ORCID 0000-0001-9785-5897
Anna M KnapinskaAlphazyme, LLC, Jupiter, Florida.
Gregg B FieldsAlphazyme, LLC, Jupiter, Florida.
Conor C LynchDepartment of Tumor Biology, University of South Florida, Tampa, Florida. conor.lynch@moffitt.org.ORCID 0000-0002-4506-6244
University of South Florida · USJupiter Medical Center · USGraz University of Technology · ATMoffitt Cancer Center · USQueens College, CUNY · USScripps Research Institute · US

Funding

Defining bone ecosystem effects on metastatic prostate cancer evolution and treatment response using an integrated mathematical modeling approachU01CA244101 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI BASANTA GUTIERREZ, DAVID, LYNCH, CONOR C · 2020 to 2024
$2.3M
Local and systemic control of multiple myeloma colonization and growth by MMP-13R01CA239214 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI LYNCH, CONOR C · 2019 to 2023
$2.2M
Specific skeletal targeting of MMP-2 for the treatment of multiple myelomaR21CA191981 · NCI · H. LEE MOFFITT CANCER CTR & RES INST · PI HAZLEHURST, LORI A, LYNCH, CONOR C · 2015 to 2016
$401k
NCI NIH HHS R01 CA239214NCI NIH HHS R21 CA191981NCI NIH HHS U01 CA244101
6 · The paper itself

Abstract

Multiple myeloma promotes systemic skeletal bone disease that greatly contributes to patient morbidity. Resorption of type I collagen-rich bone matrix by activated osteoclasts results in the release of sequestered growth factors that can drive progression of the disease. Matrix metalloproteinase-13 (MMP13) is a collagenase expressed predominantly in the skeleton by mesenchymal stromal cells (MSC) and MSC-derived osteoblasts. Histochemical analysis of human multiple myeloma specimens also demonstrated that MMP13 largely localizes to the stromal compartment compared with CD138

Indexed as

AnimalsCell DifferentiationCell Line, TumorChemokines, CXCDisease Models, AnimalDisease ProgressionFemaleHumansMaleMatrix Metalloproteinase 13Mesenchymal Stem CellsMiceMice, Inbred C57BLMice, TransgenicMultiple MyelomaOsteoblastsChemokines, CXCCxcl7 protein, mouseMatrix Metalloproteinase 13MMP13 protein, humanMmp13 protein, mouse

Identifiers

PMID33526510
PMCPMC8809361
OpenAlexW3128639880

What OpenQuestion holds

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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.