Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
- PMID: 30763276
- PMCID: PMC6410763
- DOI: 10.1530/EC-18-0506
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
Abstract
Multiple endocrine neoplasia type 2 (MEN2) is an autosomal dominant genetic disease caused by RET gene germline mutations that is characterized by medullary thyroid carcinoma (MTC) associated with other endocrine tumors. Several reports have demonstrated that the RET mutation profile may vary according to the geographical area. In this study, we collected clinical and molecular data from 554 patients with surgically confirmed MTC from 176 families with MEN2 in 18 different Brazilian centers to compare the type and prevalence of RET mutations with those from other countries. The most frequent mutations, classified by the number of families affected, occur in codon 634, exon 11 (76 families), followed by codon 918, exon 16 (34 families: 26 with M918T and 8 with M918V) and codon 804, exon 14 (22 families: 15 with V804M and 7 with V804L). When compared with other major published series from Europe, there are several similarities and some differences. While the mutations in codons C618, C620, C630, E768 and S891 present a similar prevalence, some mutations have a lower prevalence in Brazil, and others are found mainly in Brazil (G533C and M918V). These results reflect the singular proportion of European, Amerindian and African ancestries in the Brazilian mosaic genome.
Keywords: Brazil; RET; medullary thyroid carcinoma; multiple endocrine neoplasia; pheochromocytoma.
Similar articles
-
M918V RET mutation causes familial medullary thyroid carcinoma: study of 8 affected kindreds.Endocr Relat Cancer. 2016 Dec;23(12):909-920. doi: 10.1530/ERC-16-0141. Endocr Relat Cancer. 2016. PMID: 27807060
-
Medullary thyroid cancer in MEN2 pediatric/adolescent carriers of RET mutation: genotype/phenotype correlation and outcome in a retrospective series of 23 patients.Front Oncol. 2025 Jan 7;14:1464890. doi: 10.3389/fonc.2024.1464890. eCollection 2024. Front Oncol. 2025. PMID: 39839784 Free PMC article.
-
Segregation of the V804L mutation and S836S polymorphism of exon 14 of the RET gene in an extended kindred with familial medullary thyroid cancer.Clin Genet. 2003 Mar;63(3):219-23. doi: 10.1034/j.1399-0004.2003.00044.x. Clin Genet. 2003. PMID: 12694233
-
Multiple endocrine neoplasia type 2.Orphanet J Rare Dis. 2006 Nov 14;1:45. doi: 10.1186/1750-1172-1-45. Orphanet J Rare Dis. 2006. PMID: 17105651 Free PMC article. Review.
-
RET proto-oncogene mutations in multiple endocrine neoplasia type 2 and medullary thyroid carcinoma.Horm Res. 1997;47(4-6):168-78. doi: 10.1159/000185461. Horm Res. 1997. PMID: 9167949 Review.
Cited by
-
Clinical characteristics of a large familial cohort with Medullary thyroid cancer and germline Cys618Arg RET mutation in an Israeli multicenter study.Front Endocrinol (Lausanne). 2023 Oct 30;14:1268193. doi: 10.3389/fendo.2023.1268193. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 38027168 Free PMC article.
-
Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma.J Kidney Cancer VHL. 2021 Mar 13;8(1):19-24. doi: 10.15586/jkcvhl.v8i1.171. eCollection 2021. J Kidney Cancer VHL. 2021. PMID: 33777662 Free PMC article.
-
Twenty-Five Years Experience on RET Genetic Screening on Hereditary MTC: An Update on The Prevalence of Germline RET Mutations.Genes (Basel). 2019 Sep 10;10(9):698. doi: 10.3390/genes10090698. Genes (Basel). 2019. PMID: 31510104 Free PMC article.
-
A Case of Cushing's Disease and a RET Pathogenic Variant: Exploring Possible Rare Associations.Cureus. 2024 Oct 8;16(10):e71058. doi: 10.7759/cureus.71058. eCollection 2024 Oct. Cureus. 2024. PMID: 39512978 Free PMC article.
-
Medullary Thyroid Carcinoma and Associated Endocrinopathies in Slovenia from 1995 to 2021.Life (Basel). 2022 Jul 21;12(7):1091. doi: 10.3390/life12071091. Life (Basel). 2022. PMID: 35888179 Free PMC article.
References
-
- Maia AL, Ceolin L, Maciel RMB. Multiple endocrine neoplasia type 2. In Guide of Oncology. Rio de Janeiro, Brazil: Brazilian National Cancer Institute, 2016.
-
- Hoff AO, Neves LAC, Maciel RMB. Multiple endocrine neoplasia. In Endocrinology, Principles and Practice, 2nd ed., ch. 77, pp 1275–1284. Eds Saad MJA, Maciel RMB. & Mendonça BB. São Paulo, Brazil: Atheneu, 2017
LinkOut - more resources
Full Text Sources