| Literature DB >> 30136351 |
Weilai Dong1, Norman G Nicolson2,3, Jungmin Choi1, Andrea L Barbieri4, John W Kunstman2,3, Sara Abou Azar3, James Knight5, Kaya Bilguvar1,5, Shrikant M Mane1,5, Richard P Lifton1, Reju Korah2,3, Tobias Carling2,3.
Abstract
Foci of papillary or follicular thyroid carcinoma are frequently noted in thyroidectomy specimens of anaplastic thyroid carcinoma (ATC). However, whether ATCs evolve from these co-existing well-differentiated thyroid carcinomas (WDTCs) has not been well-understood. To investigate the progression of ATC in patients with co-existing WDTCs, five ATC tumors with co-existing WDTCs and matching normal tissues were whole-exome sequenced. After mapping the somatic alteration landscape, evolutionary lineages were constructed by sub-clone analysis. Though each tumor harbored at least some unique private mutations, all five ATCs demonstrated numerous overlapping mutations with matched WDTCs. Clonal analysis further demonstrated that each ATC/WDTC pair shared a common ancestor, with some pairs diverging early in their evolution and others in which the ATC seems to arise directly from a sub-clone of the WDTC. Though the precise lineal relationship remains ambiguous, based on the genetic relationship, our study clearly suggests a shared origin of ATC and WDTC.Entities:
Keywords: anaplastic thyroid carcinoma; clonal evolution; exome sequencing; well-differentiated thyroid carcinoma
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Year: 2018 PMID: 30136351 DOI: 10.1002/gcc.22678
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006