Evidence map›Paper›PMID 21422315›Full record

ArticleArchives of otolaryngology--head & neck surgery2011

The role of MAGEA2 in head and neck cancer.

Chad A Glazer, Ian M Smith, Sheetal Bhan, Wenyue Sun, Steven S Chang, Kavita M Pattani, William Westra, Zubair Khan, Joseph A Califano

Open access · greenAbstract read
In one paragraph

Article in Archives of otolaryngology--head & neck surgery, 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
0.7field-weighted citation impact, top 30% 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, 23 citations in OpenAlex.

  1. Article
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  4. Expression dynamics ofOncotarget · 2019
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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

9 authors at 1 institution in 1 country.

Chad A GlazerDepartment of Otolaryngology-Head and Neck Surgery, The Johns Hopkins Medical Institutions, 1550 Orleans St, Room 5N.04, Baltimore, MD 21231, USA.
Ian M Smith
Sheetal Bhan
Wenyue Sun
Steven S Chang
Kavita M Pattani
William Westra
Zubair Khan
Joseph A Califano
Johns Hopkins University · US

Funding

INTEGRATED DEVELOPMENT OF NOVEL MOLECULAR MARKERSU01CA084986 · NCI · JOHNS HOPKINS UNIVERSITY · PI SIDRANSKY, DAVID · 1999 to 2014
$33.8M
Tumor Suppressor Gene Promoter Hypermethylation for Detection of Head/Neck CancerP50CA096784 · NCI · JOHNS HOPKINS UNIVERSITY · PI SIDRANSKY, DAVID · 2002 to 2006
$11.3M
NCI NIH HHS 5P50CA096784-05NCI NIH HHS P50 CA096784NCI NIH HHS P50 CA096784-01NCI NIH HHS U01 CA084986NCI NIH HHS U01CA084986
6 · The paper itself

Abstract

objectiveTo examine the role of MAGEA2 in the tumorigenesis of head and neck squamous cell carcinoma (HNSCC).

designPrimary tissue microarray data and quantitative reverse transcription-polymerase chain reaction (RT-PCR) showed that MAGEA2 is differentially overexpressed in HNSCC. Functional analyses were then performed using MAGEA2 transfections and small-interfering RNA knockdowns with subsequent anchorage-dependent growth studies and cell cycle analyses. Quantitative RT-PCR was used to evaluate expression changes in p53 downstream targets after transfection of MAGEA2 into normal upper aerodigestive cell lines.

resultsMAGEA2 is differentially overexpressed in HNSCC. In addition, MAGEA2 promotes growth in normal oral keratinocytes, whereas knockdown of MAGEA2 in HNSCC cells decreases growth. Using the HCT116 p53 wt and null cell line system, transfection of MAGEA2 induced growth in the p53 wt cell line while providing no growth advantage in the p53 mutant cells. Subsequently, transfection of MAGEA2 induced a decrease in messenger RNA expression of the p53 downstream targets CDKN1A and BAX and decreased G1 arrest in cells allowed to remain confluent for longer than 48 hours.

conclusionsThese data suggest that MAGEA2 is differentially expressed in HNSCC and functions, in part, through the p53 pathway by increasing cellular proliferation and abrogating cell cycle arrest. This improved understanding of MAGEA2 function and expression patterns will potentially allow for the improved ability to use MAGEA2 for detection, surveillance, and targeted therapeutics.

Indexed as

AnimalsAntigens, NeoplasmCarcinoma, Squamous CellCell CycleCell DivisionCell Line, TumorCell Transformation, NeoplasticFibroblastsGene Expression Regulation, NeoplasticGene Knockdown TechniquesHumansKeratinocytesMiceNeoplasm StagingOligonucleotide Array Sequence AnalysisOtorhinolaryngologic NeoplasmsAntigens, NeoplasmMage-a2 antigenRNA, MessengerRNA, Small InterferingTumor Suppressor Protein p53

Identifiers

PMID21422315
PMCPMC3309612
OpenAlexW2114744666

What OpenQuestion holds

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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.