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Pan-genomic characterization of high-risk pediatric papillary thyroid carcinoma

Stenman, Adam (författare)
Karolinska Institutet
Backman, Samuel (författare)
Uppsala universitet,Endokrinkirurgi
Johansson, Klara (författare)
Karolinska Inst, Dept Oncol Pathol, Stockholm, Sweden
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Paulsson, Johan O. (författare)
Karolinska Institutet
Stålberg, Peter (författare)
Uppsala universitet,Endokrinkirurgi
Zedenius, Jan (författare)
Karolinska Institutet
Juhlin, C. Christofer (författare)
Karolinska Institutet
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 (creator_code:org_t)
2021
2021
Engelska.
Ingår i: Endocrine-Related Cancer. - 1351-0088 .- 1479-6821. ; 28:5, s. 337-351
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Pediatric papillary thyroid carcinomas (pPTCs) are often indolent tumors with excellent long- term outcome, although subsets of cases are clinically troublesome and recur. Although it is generally thought to exhibit similar molecular aberrancies as their counterpart tumors in adults, the pan-genomic landscape of clinically aggressive pPTCs has not been previously described. In this study, five pairs of primary and synchronously metastatic pPTC from patients with high-risk phenotypes were characterized using parallel whole-genome and -transcriptome sequencing. Primary tumors and their metastatic components displayed an exceedingly low number of coding somatic mutations and gross chromosomal alterations overall, with surprisingly few shared mutational events. Two cases exhibited one established gene fusion event each (SQSTM1-NTRK3 and NCOA4-RET) in both primary and metastatic tissues, and one case each was positive for a BRAF V600E mutation and a germline truncating CHEK2 mutation, respectively. One single case was without apparent driver events and was considered as a genetic orphan. Non-coding mutations in cancer-associated regions were generally not present. By expressional analyses, fusion-driven primary and metastatic pPTC clustered separately from the mutation-driven cases and the sole genetic orphan. We conclude that pPTCs are genetically indolent tumors with exceedingly stable genomes. Several mutations found exclusively in the metastatic samples which may represent novel genetic events that drive the metastatic behavior, and the differences in mutational compositions suggest early clonal divergence between primary tumors and metastases. Moreover, an overrepresentation of mutational and expressional dysregulation of immune regulatory pathways was noted among fusion-positive pPTC metastases, suggesting that these tumors might facilitate spread through immune evasive mechanisms.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

whole-genome sequencing
RNA sequencing
mutation
pediatric thyroid cancer
papillary thyroid carcinoma

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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