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Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer

Well-differentiated thyroid carcinoma (DTC) is the most common endocrine malignancy that has an excellent prognosis with a 5-year survival rate of about 98%. However, approximately 50% of the patients with DTC who present with distant metastases (advanced DTC) die from the disease within 5 years of...

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Autores principales: Tella, Sri Harsha, Kommalapati, Anuhya, Esquivel, Mary Angelynne, Correa, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524671/
https://www.ncbi.nlm.nih.gov/pubmed/28791253
http://dx.doi.org/10.3389/fonc.2017.00160
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author Tella, Sri Harsha
Kommalapati, Anuhya
Esquivel, Mary Angelynne
Correa, Ricardo
author_facet Tella, Sri Harsha
Kommalapati, Anuhya
Esquivel, Mary Angelynne
Correa, Ricardo
author_sort Tella, Sri Harsha
collection PubMed
description Well-differentiated thyroid carcinoma (DTC) is the most common endocrine malignancy that has an excellent prognosis with a 5-year survival rate of about 98%. However, approximately 50% of the patients with DTC who present with distant metastases (advanced DTC) die from the disease within 5 years of initial diagnosis even after getting the appropriate therapy. Apart from recent advancements in chemotherapy agents, the potential role of metabolic interventions, including the use of metformin, ketogenic diet, and high-dose vitamin C in the management of advanced cancers have been investigated as a less toxic co-adjuvant therapies. The role of vitamin C has been of interest again after a preclinical mice study showed that high-dose vitamin C is selectively lethal to KRAS and BRAF mutant colorectal cancer cells by targeting the glutathione pathway. This raises the possibility of utilizing high-doses of vitamin C in the treatment of aDTC where KRAS and BRAF mutations are common. Similarly, alteration of cellular metabolism by low-carbohydrate ketogenic diets can be an important therapeutic strategy to selectively kill cancer cells that mainly survive on glycolysis. Among the potential adjuvant therapies proposed in this paper, metformin is the only agent that has shown benefit in human model of aDTC, the others have shown benefit but in preclinical/animal studies only and need to be further evaluated in large clinical trials. In conclusion, in addition to concurrent chemotherapy options, these metabolic interventions may have a great potential as co-adjuvant therapy in the management of aDTC.
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spelling pubmed-55246712017-08-08 Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer Tella, Sri Harsha Kommalapati, Anuhya Esquivel, Mary Angelynne Correa, Ricardo Front Oncol Oncology Well-differentiated thyroid carcinoma (DTC) is the most common endocrine malignancy that has an excellent prognosis with a 5-year survival rate of about 98%. However, approximately 50% of the patients with DTC who present with distant metastases (advanced DTC) die from the disease within 5 years of initial diagnosis even after getting the appropriate therapy. Apart from recent advancements in chemotherapy agents, the potential role of metabolic interventions, including the use of metformin, ketogenic diet, and high-dose vitamin C in the management of advanced cancers have been investigated as a less toxic co-adjuvant therapies. The role of vitamin C has been of interest again after a preclinical mice study showed that high-dose vitamin C is selectively lethal to KRAS and BRAF mutant colorectal cancer cells by targeting the glutathione pathway. This raises the possibility of utilizing high-doses of vitamin C in the treatment of aDTC where KRAS and BRAF mutations are common. Similarly, alteration of cellular metabolism by low-carbohydrate ketogenic diets can be an important therapeutic strategy to selectively kill cancer cells that mainly survive on glycolysis. Among the potential adjuvant therapies proposed in this paper, metformin is the only agent that has shown benefit in human model of aDTC, the others have shown benefit but in preclinical/animal studies only and need to be further evaluated in large clinical trials. In conclusion, in addition to concurrent chemotherapy options, these metabolic interventions may have a great potential as co-adjuvant therapy in the management of aDTC. Frontiers Media S.A. 2017-07-25 /pmc/articles/PMC5524671/ /pubmed/28791253 http://dx.doi.org/10.3389/fonc.2017.00160 Text en Copyright © 2017 Tella, Kommalapati, Esquivel and Correa. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Tella, Sri Harsha
Kommalapati, Anuhya
Esquivel, Mary Angelynne
Correa, Ricardo
Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer
title Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer
title_full Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer
title_fullStr Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer
title_full_unstemmed Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer
title_short Potential Role of Metabolic Intervention in the Management of Advanced Differentiated Thyroid Cancer
title_sort potential role of metabolic intervention in the management of advanced differentiated thyroid cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5524671/
https://www.ncbi.nlm.nih.gov/pubmed/28791253
http://dx.doi.org/10.3389/fonc.2017.00160
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