دورية أكاديمية

RET splice site variants in medullary thyroid carcinoma

التفاصيل البيبلوغرافية
العنوان: RET splice site variants in medullary thyroid carcinoma
المؤلفون: Daryoush Saeed-Vafa, Kyriakos Chatzopoulos, Juan Hernandez-Prera, Pedro Cano, James J. Saller, Julie E. Hallanger Johnson, Bryan McIver, Theresa A. Boyle
المصدر: Frontiers in Genetics, Vol 15 (2024)
بيانات النشر: Frontiers Media S.A., 2024.
سنة النشر: 2024
المجموعة: LCC:Genetics
مصطلحات موضوعية: medullary thyroid carcinoma, RET, splice site variant, thyroid, endocrine, Genetics, QH426-470
الوصف: 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.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1664-8021
العلاقة: https://www.frontiersin.org/articles/10.3389/fgene.2024.1377158/fullTest; https://doaj.org/toc/1664-8021Test
DOI: 10.3389/fgene.2024.1377158
الوصول الحر: https://doaj.org/article/43f3651c022f4709b71eca41e706cfceTest
رقم الانضمام: edsdoj.43f3651c022f4709b71eca41e706cfce
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:16648021
DOI:10.3389/fgene.2024.1377158