Evidence map›Paper›PMID 20629091›Full record

ArticleHead & neck2011

Targeted molecular therapy of head and neck squamous cell carcinoma with the tyrosine kinase inhibitor vandetanib in a mouse model.

Daisuke Sano, David R Fooshee, Mei Zhao, Genevieve A Andrews, Mitchell J Frederick, Chad Galer, Zvonimir L Milas, Phuong Khanh H Morrow, Jeffrey N Myers

Abstract readComparative Study
In one paragraph

Article in Head & neck, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-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

11 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Article
  10. Disruptive TP53 mutation is associated with aggressive disease characteristics in an orthotopic murine model of oral tongue cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Article
  11. Vandetanib restores head and neck squamous cell carcinoma cells' sensitivity to cisplatin and radiation in vivo and in vitro.Clinical cancer research : an official journal of the American Association for Cancer Research · 2011
    Article
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

9 authors at 1 institution in 1 country.

Daisuke SanoDepartment of Head and Neck Surgery, The University of Texas M. D. Anderson Cancer Center, Houston, Texas, USA.
David R Fooshee
Mei Zhao
Genevieve A Andrews
Mitchell J Frederick
Chad Galer
Zvonimir L Milas
Phuong Khanh H Morrow
Jeffrey N Myers
The University of Texas MD Anderson Cancer Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting the p53 pathway for reversal of oral premalignancyP50CA097007 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MYERS, JEFFREY NICHOLAS · 2002 to 2012
$26.1M
TRAINING OF ACADEMIC HEAD AND NECK SURGICAL ONCOLOGISTST32CA060374 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI MYERS, JEFFREY NICHOLAS · 1995 to 2010
$797k
NCI NIH HHS CA016672NCI NIH HHS P50 CA097007NCI NIH HHS P50CA097007NCI NIH HHS T32 CA060374NCI NIH HHS T32CA60374
6 · The paper itself

Abstract

backgroundWe investigated the effects of vandetanib, an inhibitor of vascular endothelial growth factor receptor 2 (VEGFR-2) and epidermal growth factor receptor (EGFR), alone and in combination with paclitaxel in an orthotopic mouse model of human head and neck squamous cell carcinoma (HNSCC).

methodsThe in vitro effects of vandetanib (ZACTIMA) were assessed in 2 HNSCC cell lines on cell growth, apoptosis, receptor and downstream signaling molecule expression, and phosphorylation levels. We assessed in vivo effects of vandetanib and/or paclitaxel by measuring tumor cell apoptosis, endothelial cell apoptosis, microvessel density, tumor size, and animal survival.

resultsIn vitro, vandetanib inhibited the phosphorylation of EGFR and its downstream targets in HNSCC cells and inhibited proliferation and induced apoptosis of HNSCC cells and extended survival and inhibited tumor growth in nude mice orthotopically injected with human HNSCC.

conclusionVandetanib has the potential to be a novel molecular targeted therapy for HNSCC.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic Combined Chemotherapy ProtocolsApoptosisBlotting, WesternCarcinoma, Squamous CellDisease Models, AnimalErbB ReceptorsFlow CytometryHead and Neck NeoplasmsHumansMaleMiceMice, NudePaclitaxelPiperidinesErbB ReceptorsPaclitaxelPiperidinesProtein-Tyrosine KinasesQuinazolinesvandetanibVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID20629091
PMCPMC2958241
OpenAlexW1984132650

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.