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Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET.
Pediatr Surg Int. 2008 May; 24(5):521-30.PS

Abstract

Multiple endocrine neoplasia (MEN) type 2 syndromes are autosomal dominant clinical associations characterized by a common clinical feature, medullary thyroid carcinoma (MTC). The ability to accurately predict the risk by genetic RET proto-oncogene analysis has resulted in the active follow-up of children at risk for developing early metastatic tumours and which can be prevented by prophylactic thyroidectomy. The C634 and M918T mutations (associated with MEN2A and MEN2B, respectively) are particularly associated with early aggressive behavior and distant metastatic spread requiring early intervention. RET is known to be involved in cellular signalling processes during development and controls the survival, proliferation, differentiation and migration of the enteric nervous system (ENS) progenitor cells, as well as the survival and regeneration of sympathetic neural and kidney cells. The centrality of RET in the etiology of both MEN2 and HSCR is now well established with fairly consistent associations existing between RET genotype and phenotype in MEN2. The relationship between Hirschsprung's disease (HSCR) MEN2 syndromes appears to be a highly significant one, sharing a common etiological factor in the RET proto-oncogene. It is now well accepted that most HSCR arises from loss of function, RET mutations, RET haploinsufficiency or RET polymorphisms and haplotypes of the RET promotor region. MEN2 syndromes result from gene up regulation due to germline activating mutations in the RET proto-oncogene (1:500,000). MTC is mostly associated with variations in the 5 cysteine RET radicals and codon-risk management protocols are of considerable value but not infallible. Oncogenic RET mutations may, however, vary between specific population groups. RET analysis in MEN has revolutionized the management of children of MEN2 and allowed surgical prediction and prophylaxis to take place. We discuss the role of genetic testing and possible guidelines for the management of patients from MTC families. The future appears full of promise and the current evaluation of RET-targeting tyrosine kinase and other inhibitors are of considerable interest in the management of these conditions.

Authors+Show Affiliations

Faculty of Health Sciences, University of Stellenbosch, 7505, Tygerberg, South Africa. swm@sun.ac.zaNo affiliation info available

Pub Type(s)

Journal Article
Review

Language

eng

PubMed ID

18365214

Citation

Moore, S W., and M G. Zaahl. "Multiple Endocrine Neoplasia Syndromes, Children, Hirschsprung's Disease and RET." Pediatric Surgery International, vol. 24, no. 5, 2008, pp. 521-30.
Moore SW, Zaahl MG. Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET. Pediatr Surg Int. 2008;24(5):521-30.
Moore, S. W., & Zaahl, M. G. (2008). Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET. Pediatric Surgery International, 24(5), 521-30. https://doi.org/10.1007/s00383-008-2137-5
Moore SW, Zaahl MG. Multiple Endocrine Neoplasia Syndromes, Children, Hirschsprung's Disease and RET. Pediatr Surg Int. 2008;24(5):521-30. PubMed PMID: 18365214.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Multiple endocrine neoplasia syndromes, children, Hirschsprung's disease and RET. AU - Moore,S W, AU - Zaahl,M G, Y1 - 2008/03/26/ PY - 2008/03/05/accepted PY - 2008/3/28/pubmed PY - 2008/10/22/medline PY - 2008/3/28/entrez SP - 521 EP - 30 JF - Pediatric surgery international JO - Pediatr Surg Int VL - 24 IS - 5 N2 - Multiple endocrine neoplasia (MEN) type 2 syndromes are autosomal dominant clinical associations characterized by a common clinical feature, medullary thyroid carcinoma (MTC). The ability to accurately predict the risk by genetic RET proto-oncogene analysis has resulted in the active follow-up of children at risk for developing early metastatic tumours and which can be prevented by prophylactic thyroidectomy. The C634 and M918T mutations (associated with MEN2A and MEN2B, respectively) are particularly associated with early aggressive behavior and distant metastatic spread requiring early intervention. RET is known to be involved in cellular signalling processes during development and controls the survival, proliferation, differentiation and migration of the enteric nervous system (ENS) progenitor cells, as well as the survival and regeneration of sympathetic neural and kidney cells. The centrality of RET in the etiology of both MEN2 and HSCR is now well established with fairly consistent associations existing between RET genotype and phenotype in MEN2. The relationship between Hirschsprung's disease (HSCR) MEN2 syndromes appears to be a highly significant one, sharing a common etiological factor in the RET proto-oncogene. It is now well accepted that most HSCR arises from loss of function, RET mutations, RET haploinsufficiency or RET polymorphisms and haplotypes of the RET promotor region. MEN2 syndromes result from gene up regulation due to germline activating mutations in the RET proto-oncogene (1:500,000). MTC is mostly associated with variations in the 5 cysteine RET radicals and codon-risk management protocols are of considerable value but not infallible. Oncogenic RET mutations may, however, vary between specific population groups. RET analysis in MEN has revolutionized the management of children of MEN2 and allowed surgical prediction and prophylaxis to take place. We discuss the role of genetic testing and possible guidelines for the management of patients from MTC families. The future appears full of promise and the current evaluation of RET-targeting tyrosine kinase and other inhibitors are of considerable interest in the management of these conditions. SN - 0179-0358 UR - https://www.unboundmedicine.com/medline/citation/18365214/Multiple_endocrine_neoplasia_syndromes_children_Hirschsprung's_disease_and_RET_ L2 - https://doi.org/10.1007/s00383-008-2137-5 DB - PRIME DP - Unbound Medicine ER -