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Papers by Patricia Castro

Research paper thumbnail of Intragenic Mutations in Thyroid Cancer

Endocrinology and Metabolism Clinics of North America, 2008

The close genotype-phenotype relationship that characterizes thyroid oncology stimulated the auth... more The close genotype-phenotype relationship that characterizes thyroid oncology stimulated the authors to address this article by using a mixed, genetic and phenotypic approach. Within the group of well differentiated carcinomas, RET/PTC1 and the BRAF V600E mutation tend to concentrate in cases of conventional papillary carcinoma (PTC); RET/PTC3 and, perhaps, BRAF VK600-1E appear to be associated with the solid variant of PTC; N-RAS Q61R and BRAF K601E mutations tend to concentrate in cases of the follicular variant of PTC (FVPTC), while a PAX8-peroxisome proliferator-activated receptor-g (PPARg) rearrangement is found in benign and malignant tumors displaying a prominent follicular growth pattern (follicular thyroid adenoma or FTA, follicular thyroid carcinoma or FTC, and FVPTC). The same holds true regarding Hu¨rthle cell tumors (HCT) and anaplastic thyroid carcinomas (ATC), which also present quite characteristic genetic alterations.

Research paper thumbnail of Intragenic Mutations in Thyroid Cancer

Endocrinology and Metabolism Clinics of North America, 2008

The close genotype-phenotype relationship that characterizes thyroid oncology stimulated the auth... more The close genotype-phenotype relationship that characterizes thyroid oncology stimulated the authors to address this article by using a mixed, genetic and phenotypic approach. Within the group of well differentiated carcinomas, RET/PTC1 and the BRAF V600E mutation tend to concentrate in cases of conventional papillary carcinoma (PTC); RET/PTC3 and, perhaps, BRAF VK600-1E appear to be associated with the solid variant of PTC; N-RAS Q61R and BRAF K601E mutations tend to concentrate in cases of the follicular variant of PTC (FVPTC), while a PAX8-peroxisome proliferator-activated receptor-g (PPARg) rearrangement is found in benign and malignant tumors displaying a prominent follicular growth pattern (follicular thyroid adenoma or FTA, follicular thyroid carcinoma or FTC, and FVPTC). The same holds true regarding Hu¨rthle cell tumors (HCT) and anaplastic thyroid carcinomas (ATC), which also present quite characteristic genetic alterations.

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