Evidence map›Paper›PMID 26265694›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2015

Pretreatment microRNA Expression Impacting on Epithelial-to-Mesenchymal Transition Predicts Intrinsic Radiosensitivity in Head and Neck Cancer Cell Lines and Patients.

Monique C de Jong, Jelle J Ten Hoeve, Reidar Grénman, Lodewyk F Wessels, Ron Kerkhoven, Hein Te Riele, Michiel W M van den Brekel, Marcel Verheij, Adrian C Begg

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
3.5field-weighted citation impact, top 7% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Biological tumor markers associated with local control after primary radiotherapy in laryngeal cancer: A systematic review.Clinical otolaryngology : official journal of ENT-UK ; official journal of Netherlands Society for Oto-Rhino-Laryngology & Cervico-Facial Surgery · 2020
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  14. Machine Learning & Molecular Radiation Tumor Biomarkers.Seminars in radiation oncology · 2023
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  15. Application of nano-radiosensitizers in combination cancer therapy.Bioengineering & translational medicine · 2023
    Review
  16. Article
  17. Radiotherapy resistance: identifying universal biomarkers for various human cancers.Journal of cancer research and clinical oncology · 2022
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 2 countries.

Monique C de JongDepartment of Biological Stress Response, The Netherlands Cancer Institute, Amsterdam, the Netherlands. Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Jelle J Ten HoeveDepartment of Computational Cancer Biology (Department of Molecular Carcinogenesis), The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Reidar GrénmanDepartment of Otorhinolaryngology-Head and Neck Surgery and Department of Medical Biochemistry, Turku University Hospital, University of Turku, Turku, Finland.
Lodewyk F WesselsDepartment of Computational Cancer Biology (Department of Molecular Carcinogenesis), The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Ron KerkhovenCentral Genomic Facility, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Hein Te RieleDepartment of Biological Stress Response, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Michiel W M van den BrekelDepartment of Head and Neck Oncology and Surgery, The Netherlands Cancer Institute, Amsterdam, the Netherlands. Department of Maxillofacial Surgery, Academic Medical Center, University of Amsterdam, Amsterdam, the Netherlands.
Marcel VerheijDepartment of Biological Stress Response, The Netherlands Cancer Institute, Amsterdam, the Netherlands. Department of Radiation Oncology, The Netherlands Cancer Institute, Amsterdam, the Netherlands. m.verheij@nki.nl.
Adrian C BeggDepartment of Biological Stress Response, The Netherlands Cancer Institute, Amsterdam, the Netherlands.
Dutch Cancer Society · NLOncode Institute · NLAmsterdam UMC Location University of Amsterdam · NLCancer Genomics Centre · NLTurku University Hospital · FI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposePredominant causes of head and neck cancer recurrence after radiotherapy are rapid repopulation, hypoxia, fraction of cancer stem cells, and intrinsic radioresistance. Currently, intrinsic radioresistance can only be assessed by ex vivo colony assays. Besides being time-consuming, colony assays do not identify causes of intrinsic resistance. We aimed to identify a biomarker for intrinsic radioresistance to be used before start of treatment and to reveal biologic processes that could be targeted to overcome intrinsic resistance. EXPERIMENTAL

designWe analyzed both microRNA and mRNA expression in a large panel of head and neck squamous cell carcinoma (HNSCC) cell lines. Expression was measured on both irradiated and unirradiated samples. Results were validated using modified cell lines and a series of patients with laryngeal cancer.

resultsmiRs, mRNAs, and gene sets that correlated with resistance could be identified from expression data of unirradiated cells. The presence of epithelial-to-mesenchymal transition (EMT) and low expression of miRs involved in the inhibition of EMT were important radioresistance determinants. This finding was validated in two independent cell line pairs, in which the induction of EMT reduced radiosensitivity. Moreover, low expression of the most important miR (miR-203) was shown to correlate with local disease recurrence after radiotherapy in a series of patients with laryngeal cancer.

conclusionsThese findings indicate that EMT and low expression of EMT-inhibiting miRs, especially miR-203, measured in pretreatment material, causes intrinsic radioresistance of HNSCC, which could enable identification and treatment modification of radioresistant tumors. Clin Cancer Res; 21(24); 5630-8. ©2015 AACR.

Indexed as

Cell Line, TumorDose-Response Relationship, RadiationEpithelial-Mesenchymal TransitionGene Expression ProfilingGene Expression Regulation, NeoplasticHead and Neck NeoplasmsHumansMicroRNAsNeoplasm StagingPrognosisProportional Hazards ModelsRadiation DosageRadiation ToleranceTime FactorsTranscriptomeMicroRNAs

Identifiers

PMID26265694
OpenAlexW1942614232

What OpenQuestion holds

Textmetadata
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.