Evidence map›Paper›PMID 21454012›Full record

ArticleCancer letters2011

CXCR4 suppression attenuates EGFRvIII-mediated invasion and induces p38 MAPK-dependent protein trafficking and degradation of EGFRvIII in breast cancer cells.

Massod Rahimi, Theodore A Toth, Careen K Tang

Open access · greenAbstract read
In one paragraph

Article in Cancer letters, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. CoClOncology letters · 2018
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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

3 authors at 1 institution in 1 country.

Massod RahimiLombardi Comprehensive Cancer Center, Department of Oncology, Georgetown University Medical Center, Washington, DC 20057, United States.
Theodore A Toth
Careen K Tang
Georgetown University Medical Center · US

Funding

Molecular Mechanisms of Blockage of ErbB receptorsR01CA106429 · NCI · GEORGETOWN UNIVERSITY · PI TANG, CAREEN K · 2005 to 2009
$1.2M
NCI NIH HHS R01 CA106429NCI NIH HHS R01CA106429
6 · The paper itself

Abstract

Our previous report has shown that the constitutively activated EGFR variant, EGFRvIII, up-regulates the pro-metastatic chemokine receptor CXCR4 in breast cancer cells. Here we evaluated the biological effect and cell signaling effects of silencing CXCR4 expression in EGFRvIII-expressing breast cancer cells. Short hairpin RNA (shRNA)-mediated suppression of CXCR4 expression significantly reduced the invasive potential and proliferation of EGFRvIII-expressing breast cancer cells. These cells exhibited a reduction of EGFRvIII activity and protein expression due to increased protein degradation and altered protein trafficking. In conclusion, suppression of CXCR4 inhibits EGFRvIII-mediated breast cancer cell invasion and proliferation.

Indexed as

Gene Expression Regulation, NeoplasticBreast NeoplasmsCell Line, TumorCell ProliferationCell SeparationErbB ReceptorsFemaleFlow CytometryGene SilencingHumansModels, BiologicalNeoplasm Invasivenessp38 Mitogen-Activated Protein KinasesProteasome Endopeptidase ComplexProtein TransportReceptors, CXCR4epidermal growth factor receptor VIIIErbB Receptorsp38 Mitogen-Activated Protein KinasesProteasome Endopeptidase ComplexReceptors, CXCR4

Identifiers

PMID21454012
PMCPMC3100082
OpenAlexW2116694683

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.