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Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma

Four proto-oncogenes commonly associated with well-differentiated thyroid carcinoma, rearranged during transfection (RET)/papillary thyroid cancer, BRAF, RAS, and PAX8/peroxisome proliferator activated receptor-γ, may carry diagnostic and prognostic significance. These oncogenes can be used to impro...

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Detalles Bibliográficos
Autor principal: Kim, Jung Guk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Endocrine Society 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192816/
https://www.ncbi.nlm.nih.gov/pubmed/25309777
http://dx.doi.org/10.3803/EnM.2014.29.3.211
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author Kim, Jung Guk
author_facet Kim, Jung Guk
author_sort Kim, Jung Guk
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description Four proto-oncogenes commonly associated with well-differentiated thyroid carcinoma, rearranged during transfection (RET)/papillary thyroid cancer, BRAF, RAS, and PAX8/peroxisome proliferator activated receptor-γ, may carry diagnostic and prognostic significance. These oncogenes can be used to improve the diagnosis and management of well-differentiated thyroid carcinoma. Limited therapeutic options are available for patients with metastatic well-differentiated thyroid cancer, necessitating the development of novel therapies. Vascular endothelial growth factor (VEGF)- and RET-directed therapies such as sorafenib, motesanib, and sunitinib have been shown to be the most effective at inducing clinical responses and stabilizing the disease process. Further clinical trials of these therapeutic agents may soon change the management of thyroid cancer.
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spelling pubmed-41928162014-10-10 Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma Kim, Jung Guk Endocrinol Metab (Seoul) Review Article Four proto-oncogenes commonly associated with well-differentiated thyroid carcinoma, rearranged during transfection (RET)/papillary thyroid cancer, BRAF, RAS, and PAX8/peroxisome proliferator activated receptor-γ, may carry diagnostic and prognostic significance. These oncogenes can be used to improve the diagnosis and management of well-differentiated thyroid carcinoma. Limited therapeutic options are available for patients with metastatic well-differentiated thyroid cancer, necessitating the development of novel therapies. Vascular endothelial growth factor (VEGF)- and RET-directed therapies such as sorafenib, motesanib, and sunitinib have been shown to be the most effective at inducing clinical responses and stabilizing the disease process. Further clinical trials of these therapeutic agents may soon change the management of thyroid cancer. Korean Endocrine Society 2014-09 2014-09-25 /pmc/articles/PMC4192816/ /pubmed/25309777 http://dx.doi.org/10.3803/EnM.2014.29.3.211 Text en Copyright © 2014 Korean Endocrine Society http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kim, Jung Guk
Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma
title Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma
title_full Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma
title_fullStr Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma
title_full_unstemmed Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma
title_short Molecular Pathogenesis and Targeted Therapies in Well-Differentiated Thyroid Carcinoma
title_sort molecular pathogenesis and targeted therapies in well-differentiated thyroid carcinoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4192816/
https://www.ncbi.nlm.nih.gov/pubmed/25309777
http://dx.doi.org/10.3803/EnM.2014.29.3.211
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