Evidence map›Paper›PMID 27050077›Full record

ArticleOncotarget2016

Osteopontin is a multi-faceted pro-tumorigenic driver for central nervous system lymphoma.

Qiu Yushi, Zhimin Li, Christina A Von Roemeling, Heike Doeppler, Laura A Marlow, Betty Y S Kim, Derek C Radisky, Peter Storz, John A Copland, Han W Tun

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

16 citing papers in PubMed, 26 citations in OpenAlex.

  1. SPP1BMC medicine · 2026
    Article
  2. Spatial Location of SPP1Cancer science · 2026
    Article
  3. Article
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  6. Review
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  11. Article
  12. Review
  13. Article
  14. Review
  15. Human osteopontin: Potential clinical applications in cancer (Review).International journal of molecular medicine · 2017
    Review
  16. Review
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

10 authors at 2 institutions in 1 country.

Qiu YushiDepartment of Cancer Biology, Jacksonville, Florida, USA.
Zhimin LiDepartment of Cancer Biology, Jacksonville, Florida, USA.
Christina A Von RoemelingMayo Graduate School, Mayo Clinic, Rochester, Minnesota, USA.
Heike DoepplerDepartment of Cancer Biology, Jacksonville, Florida, USA.
Laura A MarlowDepartment of Cancer Biology, Jacksonville, Florida, USA.
Betty Y S KimDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, USA.
Derek C RadiskyDepartment of Cancer Biology, Jacksonville, Florida, USA.
Peter StorzDepartment of Cancer Biology, Jacksonville, Florida, USA.
John A CoplandDepartment of Cancer Biology, Jacksonville, Florida, USA.
Han W TunDepartment of Cancer Biology, Jacksonville, Florida, USA.
Mayo Clinic in Florida · USMayo Clinic · US

Funding

Biophysical and Biochemical Effects of the ECM on Breast Epithelial CellsR01CA187692 · NCI · PRINCETON UNIVERSITY · PI NELSON, CELESTE M, RADISKY, DEREK C · 2015 to 2019
$2.1M
RhoB in cancer pathogenesis and as a target in combinatorial therapyR01CA136665 · NCI · MAYO CLINIC JACKSONVILLE · PI COPLAND, JOHN A., SMALLRIDGE, ROBERT · 2010 to 2014
$1.6M
Protein Kinase D in oncogenic oxidative stress signalingR01CA140182 · NCI · MAYO CLINIC JACKSONVILLE · PI STORZ, PETER · 2010 to 2014
$1.5M
Osteopontin-mediated invasion and dissemination in central nervous system lymphomR21NS075509 · NINDS · MAYO CLINIC JACKSONVILLE · PI TUN, HAN W · 2012 to 2013
$419k
NCI NIH HHS R01 CA136665NCI NIH HHS R01 CA140182NCI NIH HHS R01 CA187692NINDS NIH HHS R21 NS075509
6 · The paper itself

Abstract

Osteopontin (OPN) is the most upregulated gene in primary central nervous system lymphoma (PCNSL) compared to non-CNS diffuse large B cell lymphoma (DLBCL). We show here that OPN is a key mediator of intracerebral tumor growth, invasion, and dissemination in CNS lymphoma, and that these effects depend upon activation of NF-κB. We further show that activation of NF-κB by OPN occurs through a unique mechanism in which intracellular OPN (iOPN) causes transcriptional downregulation of the NF-κB inhibitors, A20/TNFAIP3 and ABIN1/TNIP1, and secretory OPN (sOPN) promotes receptor-mediated activation of NF-κB. We also identify NF-κB-mediated induction of matrix metalloproteinase-8 (MMP-8) as a specific feature of OPN-mediated tissue invasion. These results implicate OPN as a candidate for development of targeted therapy for patients with PCNSL.

Indexed as

Cell MovementCell ProliferationAnimalsAutocrine CommunicationCell Line, TumorCentral Nervous System NeoplasmsDNA-Binding ProteinsGene Expression Regulation, NeoplasticHumansLymphoma, B-CellMatrix Metalloproteinase 8Mice, NudeNeoplasm InvasivenessNeoplasm MetastasisNF-kappa BOsteopontinDNA-Binding ProteinsMatrix Metalloproteinase 8MMP8 protein, humanNF-kappa BOsteopontinSPP1 protein, humanTNFAIP3 protein, humanTNIP1 protein, humanTumor Necrosis Factor alpha-Induced Protein 3CNS lymphomainvasionNF-κB signalingosteopontin (OPN)proliferation

Identifiers

PMID27050077
PMCPMC5078004
OpenAlexW2332257686

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.