Evidence map›Paper›PMID 24962026›Full record

ArticleCancer research2014

Neuronal pentraxin 2 supports clear cell renal cell carcinoma by activating the AMPA-selective glutamate receptor-4.

Christina A von Roemeling, Derek C Radisky, Laura A Marlow, Simon J Cooper, Stefan K Grebe, Panagiotis Z Anastasiadis, Han W Tun, John A Copland

Abstract read
In one paragraph

Article in Cancer research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

140 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  19. The prognostic and immune significance ofTranslational cancer research · 2025
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80 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

8 authors.

Christina A von RoemelingDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida.
Derek C RadiskyDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida.
Laura A MarlowDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida.
Simon J CooperDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida.
Stefan K GrebeDivision of Clinical Biochemistry and Immunology, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Panagiotis Z AnastasiadisDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida.
Han W TunDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida. Division of Hematology and Oncology, Mayo Clinic, Jacksonville, Florida.
John A CoplandDepartment of Cancer Biology, Mayo Clinic Comprehensive Cancer Center, Jacksonville, Florida. copland.john@mayo.edu.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
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
TGF Beta receptor biology in human renal cell carcinomaR01CA104505 · NCI · MAYO CLINIC JACKSONVILLE · PI COPLAND, JOHN A. · 2004 to 2009
$1.4M
NCI NIH HHS P30 CA015083NCI NIH HHS R01 CA104505NCI NIH HHS R01CA104505NCI NIH HHS R01CA104505-05S1NCI NIH HHS R01 CA136665NCI NIH HHS R01CA136665
6 · The paper itself

Abstract

Clear cell renal cell carcinoma (ccRCC) is the most common subtype of kidney cancer and has the highest propensity to manifest as metastatic disease. Recent characterizations of the genetic signature of ccRCC have revealed several factors correlated with tumor cell migration and invasion; however, the specific events driving malignancy are not well defined. Furthermore, there remains a lack of targeted therapies that result in long-term, sustainable response in patients with metastatic disease. We show here that neuronal pentraxin 2 (NPTX2) is overexpressed specifically in ccRCC primary tumors and metastases, and that it contributes to tumor cell viability and promotes cell migration through its interaction with the α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor subunit GluR4. We propose NPTX2 as a novel molecular target for therapy for patients with ccRCC diagnosed with or at risk of developing metastatic disease.

Indexed as

alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidCarcinoma, Renal CellCell Line, TumorCell MovementCell SurvivalC-Reactive ProteinHumansKidney NeoplasmsNeoplasm MetastasisNerve Tissue ProteinsPentraxinsReceptors, AMPAalpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidC-Reactive Proteinglutamate receptor ionotropic, AMPA 4Nerve Tissue ProteinsPentraxinsReceptors, AMPA

Identifiers

PMID24962026
PMCPMC4154999

What OpenQuestion holds

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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.