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Updated: Jun 29, 2025

Spontaneous Murine Model of Anaplastic Thyroid Cancer
Published on: February 3, 2023
RET splice site variants in medullary thyroid carcinoma
Daryoush Saeed-Vafa1, Kyriakos Chatzopoulos1, Juan Hernandez-Prera1
1H. Lee Moffitt Cancer Center, Tampa, FL, United States.
Abstract:
Introduction: Medullary thyroid carcinoma (MTC) is an aggressive cancer that is often caused by driver mutations in RET. Splice site variants (SSV) reflect changes in mRNA processing, which may alter protein function. RET SSVs have been described in thyroid tumors in general but have not been extensively studied in MTC. Methods: The prevalence of RET SSVs was evaluated in 3,624 cases with next generation sequence reports, including 25 MTCs. Fisher exact analysis was performed to compare RET SSV frequency in cancers with/without a diagnosis of MTC. Results: All 25 MTCs had at least one of the two most common RET SSVs versus 0.3% of 3,599 cancers with other diagnoses (p < 0.00001). The 11 cancers with non-MTC diagnoses that had the common RET SSVs were 4 neuroendocrine cancers, 4 non-small cell lung carcinomas, 2 non-MTC thyroid cancers, and 1 melanoma. All 25 MTCs analyzed had at least one of the two most common RET SSVs, including 4 with no identified mutational driver. Discussion: The identification of RET SSVs in all MTCs, but rarely in other cancer types, demonstrates that these RET SSVs distinguish MTCs from other cancer types. Future studies are needed to investigate whether these RET SSVs play a pathogenic role in MTC.
Insights
Medullary thyroid carcinoma (MTC) frequently harbors RET splice site variants (SSVs). These RET SSVs were found in all MTC cases studied, distinguishing them from other cancers and suggesting a potential diagnostic role.
Area of Science:
- Oncology
- Genetics
- Molecular Biology
Background:
- Medullary thyroid carcinoma (MTC) is an aggressive malignancy often driven by mutations in the RET proto-oncogene.
- Splice site variants (SSVs) can alter mRNA processing and protein function, but their role in MTC is not well-established.
Purpose of the Study:
- To investigate the prevalence and diagnostic potential of RET splice site variants (SSVs) in medullary thyroid carcinoma (MTC).
Main Methods:
- Next-generation sequencing data from 3,624 cancer cases, including 25 MTCs, were analyzed for RET SSVs.
- Fisher exact tests were used to compare the frequency of RET SSVs between MTC and other cancer types.
Main Results:
- All 25 MTC cases (100%) exhibited at least one of the two most common RET SSVs.
- In contrast, only 0.3% of 3,599 non-MTC cancer cases harbored these common RET SSVs (p < 0.00001).
- Notably, 4 MTC cases lacked other identified RET driver mutations, highlighting the significance of SSVs.
Conclusions:
- The high prevalence of specific RET SSVs in MTC, coupled with their rarity in other cancers, suggests they are strong distinguishing markers for MTC.
- Further research is warranted to elucidate the pathogenic role of these RET SSVs in MTC development.
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