Evidence map›Paper›PMID 35409179›Full record

ReviewInternational journal of molecular sciences2022

Sindhu Nair, James A Bonner, Markus Bredel

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
9.9field-weighted citation impact, top 1% 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

52 citing papers in PubMed, 70 citations in OpenAlex.

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  9. The role of kinase domain dimerization in EGFR activation.Structure (London, England : 1993) · 2026
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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.

Sindhu NairO'Neal Comprehensive Cancer Center, Department of Radiation Oncology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35233, USA.
James A BonnerO'Neal Comprehensive Cancer Center, Department of Radiation Oncology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35233, USA.
Markus BredelO'Neal Comprehensive Cancer Center, Department of Radiation Oncology, The University of Alabama at Birmingham Heersink School of Medicine, Birmingham, AL 35233, USA.ORCID 0000-0002-7828-0984
University of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

EGFR is a prototypical receptor tyrosine kinase that is overexpressed in multiple cancers including head and neck squamous cell carcinoma (HNSCC). The standard of care for HNSCC remains largely unchanged despite decades of research. While EGFR blockade is an attractive target in HNSCC patients and anti-EGFR strategies including monoclonal antibodies and kinase inhibitors have shown some clinical benefit, efficacy is often due to the eventual development of resistance. In this review, we discuss how the acquisition of mutations in various domains of the EGFR gene not only alter drug binding dynamics giving rise to resistance, but also how mutations can impact radiation response and overall survival in HNSCC patients. A better understanding of the EGFR mutational landscape and its dynamic effects on treatment resistance hold the potential to better stratify patients for targeted therapies in order to maximize therapeutic benefits.

Indexed as

Head and Neck NeoplasmsAntibodies, MonoclonalCell Line, TumorErbB ReceptorsHumansMutationSquamous Cell Carcinoma of Head and NeckAntibodies, MonoclonalEGFR protein, humanErbB ReceptorsEGFRhead and neck squamous cell carcinomakinase inhibitorsresistance

Identifiers

PMID35409179
PMCPMC8999014
OpenAlexW4220984447

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.