Article
[The RET gene and medullary thyroid cancer: from mutations to the planning of therapy].
Chirurgia italiana - 1 Jan 2000
Conzo Giovanni, Ruggiero Roberto, Palazzo Antonietta, Della Pietra Cristina, Stanzione Francesco, Livrea Antonio, Docimo Giovanni
Abstract excerpt
The RET gene codes for a tyrosine kinase receptor, expressed in neural crest derived cells playing a central role during embryogenesis. The RET proto-oncogene is responsible for medullary thyroid cancer and multiple endocrine neoplasia type 2. To date, more than 50 germline point mutations have been described. A specific correlation between genotype and phenotype is well recognized. Genetic testing is predictive...
Topics
- Carcinoma, Medullary
- Humans
- Mutation
- Proto-Oncogene Mas
- Proto-Oncogene Proteins c-ret
- Thyroid Neoplasms
