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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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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. |
format | Online Article Text |
id | pubmed-5421862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
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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