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April 5, 2026Cancer Research0 citations

Abstract 5013: Comprehensive characterization of DICER1 mutations and two hit tumorigenesis mechanisms in follicular thyroid carcinoma using multi-omics analysis

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DLDakyung LeeYLYoung Ah LeeYKYeonju Kyoung

Key Points

  • This research aims to understand how DICER1 mutations and regulatory networks contribute to follicular thyroid carcinoma.
  • Analyzed DICER1-mutant follicular thyroid carcinoma using whole-exome sequencing and RNA sequencing.
  • Compared mutant tumors with wild-type using multi-omics approaches.
  • Classified tumors as syndrome-associated or sporadic for comparative analysis.
  • Conducted integrative analyses including pathway enrichment and network modeling.
  • Sporadic tumor patients were significantly younger than wild-type patients.
  • Most tumors showed biallelic disruption via RNase IIIb mutations and secondary loss-of-function events.
  • DICER1-mutant tumors exhibited upregulation of cell-cycle, mTOR, and Wnt pathways, with suppressed immune programs.
  • Identification of a DICER1-specific cell-cycle module and a shared Wnt/MAPK module in network analysis.

Abstract

Abstract Background: DICER1 is an essential RNase III enzyme for microRNA (miRNA) processing. Germline loss-of-function (LoF) variants cause DICER1 syndrome and predispose younger individuals to tumors including follicular thyroid carcinoma (FTC). Somatic RNase IIIb hotspot mutations are characteristic, but how germline LoF, somatic hits, and tissue-specific regulatory networks drive FTC is not fully understood. Methods: We analyzed DICER1-mutant FTC (n=20) using whole-exome sequencing, miRNA-seq, RNA-seq, and proteomics, and compared them with wild-type tumors (wt-T, n=61). Tumors were classified as syndrome-associated (syn-T, n=7) or sporadic (spo-T, n=13). Integrative analyses included allelic imbalance, pathway enrichment, and network modeling (WGCNA). Results: Clinically, spo-T patients were significantly younger than wt-T, indicating an age-specific window for DICER1-driven FTC. Most tumors showed biallelic disruption through RNase IIIb hotspot mutations with secondary LoF events, and allelic imbalance confirmed two-hit inactivation even when only one mutation was detected.In syndrome-normal tissues, substantial mRNA dysregulation occurred without miRNA changes, suggesting DICER1 haploinsufficiency acts independently of global miRNA loss.In DICER1-mutant tumors, cell-cycle, mTOR, and Wnt pathways were strongly upregulated, whereas immune programs were broadly suppressed. The thyroid stem-cell marker REXO1 was specifically elevated, indicating a stem-like phenotype. Network analysis highlighted CTNNB1 and let-7i as key regulators of the DICER1 transcriptional program. Although DICER1- and RAS-mutant FTCs shared some downstream signaling modules, DICER1-mutant tumors retained a distinct expression identity. WGCNA identified a DICER1-specific cell-cycle module and a partially shared DICER1-RAS Wnt/MAPK module. Conclusion: DICER1 functions as a distinct oncogenic driver in FTC, following a biallelic inactivation model and producing unique proliferative, immune-suppressed, and stem-like transcriptional states. These findings refine the mechanism of DICER1-associated thyroid tumorigenesis and suggest potential lineage-specific therapeutic targets. Citation Format: Dakyung Lee, Young Ah Lee, Yeonju Kyoung, Seong-Keun Yoo, Sun-Wha Im, Jaeyong Choi, Yoo Hyung Kim, Dohyun Han, Young Joo Park, Jong-Il Kim. Comprehensive characterization of DICER1 mutations and two hit tumorigenesis mechanisms in follicular thyroid carcinoma using multi-omics analysis abstract. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 1 (Regular Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(7 Suppl):Abstract nr 5013.

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Lee et al. (2026) studied this question.

synapsesocial.com/papers/69d1fd4ea79560c99a0a3505https://doi.org/10.1158/1538-7445.am2026-5013
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