# Somatic Mutational Landscape in Follicular Thyroid Cancer: Insights from AACR GENIE Data

**Authors:** Beau Hsia, Julia Kuzniar, Joey Luzarraga, Asritha Sure, Vinay Veluvolu, Eli Oved, Peter T. Silberstein, Joseph Thirumalareddy, Abubakar Tauseef, Vijay Patel, Aliasgher Khaku

PMC · DOI: 10.3390/jpm16010003 · Journal of Personalized Medicine · 2025-12-21

## TL;DR

This study analyzed genetic mutations in follicular thyroid cancer to identify patterns and differences between adult and pediatric cases, aiming to improve personalized treatments.

## Contribution

The study provides new insights into the mutational landscape of follicular thyroid cancer, highlighting molecular differences between age groups and tumor stages.

## Key findings

- NRAS was the most common mutation in follicular thyroid cancer, followed by TERT and DICER1.
- DICER1 mutations were significantly more frequent in pediatric cases compared to adults.
- Metastatic tumors showed higher NRAS mutation rates than primary tumors.

## Abstract

Objective(s): To delineate the somatic mutational landscape of follicular thyroid carcinoma (FTC) from a large, real-world cohort to identify molecular subtypes and actionable targets for personalized therapeutic interventions. Methods: Genomic and clinical data for 168 FTC samples were retrieved from the AACR Project GENIE® registry via cBioPortal. This study assessed mutation frequencies, copy number alterations, and subgroup differences (primary vs. metastatic; adult vs. pediatric) using statistical tests. Results: NRAS was the most common mutation (33.9%), followed by TERT (22.6%), DICER1 (15.5%), HRAS (11.9%), and PTEN (10.7%). DICER1 mutations were significantly enriched in pediatric cases (44.4% vs. 4.6% in adults, p < 0.001), while TERT mutations were exclusive to adults (42%). NRAS mutations were more frequent in metastatic tumors (42.4%) than primary tumors (29.2%). Conclusions: FTC tumorigenesis is driven by distinct molecular pathways, with significant heterogeneity between pediatric and adult patients as well as primary and metastatic disease. These findings underscore the necessity of molecular profiling for patient stratification and provide a strong rationale for developing personalized treatment strategies to improve clinical outcomes.

## Linked entities

- **Genes:** NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893], TERT (telomerase reverse transcriptase) [NCBI Gene 7015], DICER1 (dicer 1, ribonuclease III) [NCBI Gene 23405], HRAS (HRas proto-oncogene, GTPase) [NCBI Gene 3265], PTEN (phosphatase and tensin homolog) [NCBI Gene 5728]
- **Diseases:** follicular thyroid carcinoma (MONDO:0005034), follicular thyroid cancer (MONDO:0005034)

## Full-text entities

- **Genes:** TERT (telomerase reverse transcriptase) [NCBI Gene 7015] {aka CMM9, DKCA2, DKCB4, EST2, PFBMFT1, TCS1}, PTEN (phosphatase and tensin homolog) [NCBI Gene 5728] {aka 10q23del, BZS, CWS1, DEC, GLM2, MHAM}, HRAS (HRas proto-oncogene, GTPase) [NCBI Gene 3265] {aka C-BAS/HAS, C-H-RAS, C-HA-RAS1, CTLO, H-RASIDX, HAMSV}, DICER1 (dicer 1, ribonuclease III) [NCBI Gene 23405] {aka DCR1, Dicer, Dicer1e, GLOW, HERNA, K12H4.8-LIKE}, NRAS (NRAS proto-oncogene, GTPase) [NCBI Gene 4893] {aka ALPS4, CMNS, N-ras, NCMS, NRAS1, NS6}
- **Diseases:** Follicular Thyroid Cancer (MESH:C572845), tumors (MESH:D009369), FTC (MESH:D018263)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12843263/full.md

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12843263/full.md

## References

41 references — full list in the complete paper: https://tomesphere.com/paper/PMC12843263/full.md

---
Source: https://tomesphere.com/paper/PMC12843263