Evidence map›Paper›PMID 29165687›Full record

ArticleJournal of the National Cancer Institute2018

Investigation of the Relationship Between Radiation Dose and Gene Mutations and Fusions in Post-Chernobyl Thyroid Cancer.

Alexey A Efanov, Alina V Brenner, Tetiana I Bogdanova, Lindsey M Kelly, Pengyuan Liu, Mark P Little, Abigail I Wald, Maureen Hatch, Liudmyla Y Zurnadzy, Marina N Nikiforova and 6 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in Journal of the National Cancer Institute, 2018. 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 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

  1. Guideline
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  12. Thyroid Cancer in Regions Most Contaminated after the Chernobyl Disaster.Journal of biomedical physics & engineering · 2024
    Article
  13. Article
  14. Radiation-Related Thyroid Cancer.Endocrine reviews · 2024
    Review
  15. Progress in Thyroid Cancer Genomics: A 40-Year Journey.Thyroid : official journal of the American Thyroid Association · 2023
    Review
  16. Review
  17. Review
  18. Molecular Landscape of Pediatric Thyroid Cancer: A Review.Diagnostics (Basel, Switzerland) · 2022
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 3 countries.

Alexey A EfanovDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Alina V BrennerDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Tetiana I BogdanovaState Institution V. P. Komisarenko Institute of Endocrinology and Metabolism of AMS of Ukraine, Kyiv, Ukraine.
Lindsey M KellyDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Pengyuan LiuSir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Mark P LittleDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Abigail I WaldDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Maureen HatchDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Liudmyla Y ZurnadzyState Institution V. P. Komisarenko Institute of Endocrinology and Metabolism of AMS of Ukraine, Kyiv, Ukraine.
Marina N NikiforovaDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
Vladimir DrozdovitchDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Rebecca Leeman-NeillColumbia University Medical Center, New York, NY.
Kiyohiko MabuchiDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Mykola D TronkoState Institution V. P. Komisarenko Institute of Endocrinology and Metabolism of AMS of Ukraine, Kyiv, Ukraine.
Stephen J ChanockDivision of Cancer Epidemiology and Genetics, National Cancer Institute, National Institutes of Health, Bethesda, MD.
Yuri E NikiforovDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, PA.
University of Pittsburgh · USNational Cancer Institute · USNational Institutes of Health · USV.P. Komisarenko Institute of Endocrinology and Metabolism · UAColumbia University Irving Medical Center · USZhejiang University · CN

Funding

Studies of Populations Exposed to Environmental Sources of RadiationZIACP010132 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI CAHOON, ELIZABETH · 2009 to 2025
$35.2M
Mechanisms of RET/PTC rearrangements in thyroid cancerR01CA088041 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI NIKIFOROV, YURI E · 2001 to 2017
$3.8M
NCI NIH HHS R01 CA088041
6 · The paper itself

Abstract

Background: Exposure to ionizing radiation during childhood is a well-established risk factor for thyroid cancer. However, the genetic mechanisms of radiation-associated carcinogenesis remain not fully understood. Methods: In this study, we used targeted next-generation sequencing and RNA-Seq to study 65 papillary thyroid cancers (PTCs) from patients in the Ukrainian-American cohort with measurement-based iodine-131 (I-131) thyroid doses received as a result of the Chernobyl accident. We fitted linear regression models to evaluate differences in distribution of risk factors for PTC according to type of genetic alteration and logistic regression models to evaluate the I-131 dose response. All statistical tests were two-sided. Results: Driver mutations were identified in 96.9% of these thyroid cancers, including point mutations in 26.2% and gene fusions in 70.8% of cases. Novel driver fusions such as POR-BRAF, as well as STRN-ALK fusions that have not been implicated in radiation-associated cancer before, were found. The mean I-131 dose in cases with point mutations was 0.2 Gy (range = 0.013-1.05 Gy), statistically significantly lower than 1.4 Gy (range = 0.009-6.15 Gy) for cases with fusions (P < .001). No driver point mutations were found in tumors from individuals who received more than 1.1 Gy of radiation. Relative to tumors with point mutations, the proportion of tumors with gene fusions increased with radiation dose, reaching 87.8% among individuals exposed to 0.3 Gy or higher. With a limited study sample size, the estimated odds ratio at 1 Gy was 20.01 (95% confidence interval = 2.57 to 653.02, P < .001). In addition, after controlling for I-131 dose, we found higher odds ratios for gene fusion-positive PTCs associated with several specific demographic and geographic features. Conclusions: Our data provide support for a link between I-131 thyroid dose and generation of carcinogenic gene fusions, the predominant mechanism of thyroid cancer associated with radiation exposure from the Chernobyl accident.

Indexed as

Chernobyl Nuclear AccidentGene FusionMutationAdolescentAdultAnaplastic Lymphoma KinaseBiomarkers, TumorCalmodulin-Binding ProteinsCarcinoma, PapillaryChildChild, PreschoolCohort StudiesCytochrome P-450 Enzyme SystemFemaleFollow-Up StudiesHigh-Throughput Nucleotide SequencingALK protein, humanAnaplastic Lymphoma KinaseBiomarkers, TumorBRAF protein, humanCalmodulin-Binding ProteinsCytochrome P-450 Enzyme SystemIodine-131Iodine RadioisotopesMembrane ProteinsNerve Tissue ProteinsOncogene Proteins, FusionPOR protein, humanProto-Oncogene Proteins B-rafSTRN protein, human

Identifiers

PMID29165687
PMCPMC6059206
OpenAlexW2769592305

What OpenQuestion holds

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Registered trials

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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.