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Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes

BACKGROUND: EDC1 is a novel type of antibody-drug conjugate which binds and inhibits the Na,K-ATPase on the surface of cancer cells expressing dysadherin. The purpose of this study was to determine the expression of dysadherin in different types of thyroid carcinoma, and evaluate the therapeutic pot...

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Autores principales: Jang, Samuel, Yu, Xiao-Min, Montemayor-Garcia, Celina, Ahmed, Kamal, Weinlander, Eric, Lloyd, Ricardo V., Dammalapati, Ajitha, Marshall, David, Prudent, James R., Chen, Herbert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421862/
https://www.ncbi.nlm.nih.gov/pubmed/28160550
http://dx.doi.org/10.18632/oncotarget.14904
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author Jang, Samuel
Yu, Xiao-Min
Montemayor-Garcia, Celina
Ahmed, Kamal
Weinlander, Eric
Lloyd, Ricardo V.
Dammalapati, Ajitha
Marshall, David
Prudent, James R.
Chen, Herbert
author_facet Jang, Samuel
Yu, Xiao-Min
Montemayor-Garcia, Celina
Ahmed, Kamal
Weinlander, Eric
Lloyd, Ricardo V.
Dammalapati, Ajitha
Marshall, David
Prudent, James R.
Chen, Herbert
author_sort Jang, Samuel
collection PubMed
description BACKGROUND: EDC1 is a novel type of antibody-drug conjugate which binds and inhibits the Na,K-ATPase on the surface of cancer cells expressing dysadherin. The purpose of this study was to determine the expression of dysadherin in different types of thyroid carcinoma, and evaluate the therapeutic potential of EDC1 for thyroid carcinomas. METHODS: Thyroid tissues from 158 patients were examined for dysadherin expression and correlation with clinicopathological features. Thyroid cancer cell lines were examined for the expression of dysadherin and effective dose range of EDC1. RESULTS: One in 53 benign thyroid tissues and 62% of thyroid cancers expressed dysadherin. All anaplastic and a majority of papillary thyroid cancers overexpressed dysadherin, while 25% of follicular thyroid cancers was found to be positive for dysadherin. Dysadherin expression significantly correlated with extrathyroidal extension and lymph node metastases in papillary thyroid cancer. Five of six human thyroid cancer cell lines analyzed expressed high levels of dysadherin. Of those cells lines sensitive to EDC1, half maximal effective concentrations (EC50) were observed to be between 0.125 nM and 1 nM. CONCLUSIONS: EDC1 showed selective inhibition of growth in thyroid cancer cells with moderate to high expression of dysadherin, thus could be a specific and effective treatment.
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spelling pubmed-54218622017-05-10 Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes Jang, Samuel Yu, Xiao-Min Montemayor-Garcia, Celina Ahmed, Kamal Weinlander, Eric Lloyd, Ricardo V. Dammalapati, Ajitha Marshall, David Prudent, James R. Chen, Herbert Oncotarget Research Paper BACKGROUND: EDC1 is a novel type of antibody-drug conjugate which binds and inhibits the Na,K-ATPase on the surface of cancer cells expressing dysadherin. The purpose of this study was to determine the expression of dysadherin in different types of thyroid carcinoma, and evaluate the therapeutic potential of EDC1 for thyroid carcinomas. METHODS: Thyroid tissues from 158 patients were examined for dysadherin expression and correlation with clinicopathological features. Thyroid cancer cell lines were examined for the expression of dysadherin and effective dose range of EDC1. RESULTS: One in 53 benign thyroid tissues and 62% of thyroid cancers expressed dysadherin. All anaplastic and a majority of papillary thyroid cancers overexpressed dysadherin, while 25% of follicular thyroid cancers was found to be positive for dysadherin. Dysadherin expression significantly correlated with extrathyroidal extension and lymph node metastases in papillary thyroid cancer. Five of six human thyroid cancer cell lines analyzed expressed high levels of dysadherin. Of those cells lines sensitive to EDC1, half maximal effective concentrations (EC50) were observed to be between 0.125 nM and 1 nM. CONCLUSIONS: EDC1 showed selective inhibition of growth in thyroid cancer cells with moderate to high expression of dysadherin, thus could be a specific and effective treatment. Impact Journals LLC 2017-01-30 /pmc/articles/PMC5421862/ /pubmed/28160550 http://dx.doi.org/10.18632/oncotarget.14904 Text en Copyright: © 2017 Jang et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Jang, Samuel
Yu, Xiao-Min
Montemayor-Garcia, Celina
Ahmed, Kamal
Weinlander, Eric
Lloyd, Ricardo V.
Dammalapati, Ajitha
Marshall, David
Prudent, James R.
Chen, Herbert
Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
title Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
title_full Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
title_fullStr Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
title_full_unstemmed Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
title_short Dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
title_sort dysadherin specific drug conjugates for the treatment of thyroid cancers with aggressive phenotypes
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5421862/
https://www.ncbi.nlm.nih.gov/pubmed/28160550
http://dx.doi.org/10.18632/oncotarget.14904
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