Genomic characterization of cervical lymph node metastases in papillary thyroid carcinoma following the Chornobyl accident
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Published:2024-06-13
Issue:1
Volume:15
Page:
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ISSN:2041-1723
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Container-title:Nature Communications
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language:en
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Short-container-title:Nat Commun
Author:
Morton Lindsay M.ORCID, Lee Olivia W.ORCID, Karyadi Danielle M., Bogdanova Tetiana I., Stewart Chip, Hartley Stephen W.ORCID, Breeze Charles E., Schonfeld Sara J.ORCID, Cahoon Elizabeth K.ORCID, Drozdovitch VladimirORCID, Masiuk SergiiORCID, Chepurny Mykola, Zurnadzhy Liudmyla Yu, Dai Jieqiong, Krznaric Marko, Yeager MeredithORCID, Hutchinson Amy, Hicks Belynda D.ORCID, Dagnall Casey L.ORCID, Steinberg Mia K., Jones Kristine, Jain Komal, Jordan Ben, Machiela Mitchell J., Dawson Eric T., Vij Vibha, Gastier-Foster Julie M., Bowen JayORCID, Mabuchi Kiyohiko, Hatch Maureen, Berrington de Gonzalez Amy, Getz GadORCID, Tronko Mykola D., Thomas Gerry A., Chanock Stephen J.ORCID
Abstract
AbstractChildhood radioactive iodine exposure from the Chornobyl accident increased papillary thyroid carcinoma (PTC) risk. While cervical lymph node metastases (cLNM) are well-recognized in pediatric PTC, the PTC metastatic process and potential radiation association are poorly understood. Here, we analyze cLNM occurrence among 428 PTC with genomic landscape analyses and known drivers (131I-exposed = 349, unexposed = 79; mean age = 27.9 years). We show that cLNM are more frequent in PTC with fusion (55%) versus mutation (30%) drivers, although the proportion varies by specific driver gene (RET-fusion = 71%, BRAF-mutation = 38%, RAS-mutation = 5%). cLNM frequency is not associated with other characteristics, including radiation dose. cLNM molecular profiling (N = 47) demonstrates 100% driver concordance with matched primary PTCs and highly concordant mutational spectra. Transcriptome analysis reveals 17 differentially expressed genes, particularly in the HOXC cluster and BRINP3; the strongest differentially expressed microRNA also is near HOXC10. Our findings underscore the critical role of driver alterations and provide promising candidates for elucidating the biological underpinnings of PTC cLNM.
Funder
U.S. Department of Health & Human Services | NIH | NCI | Division of Cancer Epidemiology and Genetics, National Cancer Institute
Publisher
Springer Science and Business Media LLC
Reference107 articles.
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