Evidence map›Paper›PMID 22588054›Full record

ReviewAdvances in cancer research2012

Regulation of tumor initiation and metastatic progression by Eph receptor tyrosine kinases.

Jin Chen

Open access · greenAbstract readReview
In one paragraph

Review in Advances in cancer research, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

32 citing papers in PubMed, 51 citations in OpenAlex.

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  10. Drug Conjugates for Targeting Eph Receptors in Glioblastoma.Pharmaceuticals (Basel, Switzerland) · 2020
    Article
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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

1 author at 1 institution in 1 country.

Jin ChenVA Medical Center, Tennessee Valley Healthcare System, Nashville, TN, USA
Vanderbilt University · US

Funding

Ephrin-A1 in Tumor-Endothelial Interaction During MetastasisR01CA095004 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CHEN, JIN · 2003 to 2019
$4.6M
EphA2 Receptor Tyrosine Kinase in Malignant Tumor CellR01CA114301 · NCI · VANDERBILT UNIVERSITY · PI CHEN, JIN · 2005 to 2009
$1.5M
NCI NIH HHS CA114301NCI NIH HHS CA95004NCI NIH HHS R01 CA095004NCI NIH HHS R01 CA114301
6 · The paper itself

Abstract

In recent years, a growing body of evidence has indicated that signaling molecules previously implicated in axon guidance are important regulators of multistep tumorigenesis and progression. Eph receptors and ephrins belong to this special class of molecules that play important roles in both axon guidance and cancer. Tremendous progress has been made in the past few years in both understanding the role of Eph receptors and ephrins in cancer and designing therapeutic strategies for cancer therapy. This review will focus on new advances in elucidating the contribution of Eph/ephrin molecules to key processes in tumor initiation and metastatic progression, including cancer cell proliferation, invasion and metastasis, and tumor angiogenesis.

Indexed as

AnimalsCell Transformation, NeoplasticDisease ProgressionHumansNeoplasmsReceptors, Eph FamilyReceptors, Eph Family

Identifiers

PMID22588054
PMCPMC3626259
OpenAlexW1600521913

What OpenQuestion holds

Textmetadata
LicenceTDM
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.