Please use this identifier to cite or link to this item: http://hdl.handle.net/11455/32821
標題: RET protooncogene mutations in patients with apparently sporadic medullary thyroid carcinoma
作者: Huang, C.N.
張天傑
Wu, S.L.
Chang, T.C.
Huang, S.H.
Chang, T.J.
關鍵字: RET protooncogene;medullary thyroid carcinoma;somatic mutation;germline mutation;multiple endocrine neoplasia;tyrosine kinase domain;de-novo mutation;men 2a;somatic mutations;point mutations;fmtc;families;2b;management
Project: Journal of the Formosan Medical Association
期刊/報告no:: Journal of the Formosan Medical Association, Volume 97, Issue 8, Page(s) 541-546.
摘要: 
We examined RET protooncogene mutations in sporadic medullary thyroid carcinoma (MTC), using polymerase chain reaction (PCR)-based sequencing. DNA was extracted from turner tissue and peripheral blood leukocytes of seven unrelated individuals with apparently sporadic MTC. Oligonucleotide primers were selected to amplify exons 10, 11, 13, 15, and 16 of the RET protooncogene, to examine the sequences of codons 609, 611, 618, and 620 of exon 10, codon 634 of exon 11, codon 768 of exon 13, codon 883 of exon 15, and codon 918 of exon 16. Direct DNA sequencing from PCR products was then performed. The results shelved that one patient had a somatic mutation at codon 918 (ATG-->ACG), causing a Met-->Thr substitution. One patient had a de novo germline mutation at colon 634 (TGC-->CGC), causing a Cys-->Arg substitution. Another patient had a germline mutation at codon 634 (TGC-->TTC), causing a Cys-->Phe substitution. In the remaining four cases, no RET mutations were found, Unexpectedly, two offspring of the patient (a female) with a germline mutation at codon 634 (TGC-->TTC) harbored homozygous alleles for the mutation; because the father did nor carry this mutation, the other affected allele was suspected to have resulted from a de novo germline mutation of paternal origin. One of these offspring was subsequently diagnosed as having MTC. Our findings suggest that all patients with apparently sporadic MTC should be screened for the RET protooncogene by molecular analysis to detect occult or de novo multiple endocrine neoplasia 2 (MEM 2) or familial MTC. This would allow early treatment of affected family members.
URI: http://hdl.handle.net/11455/32821
ISSN: 0929-6646
Appears in Collections:獸醫學系所

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