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Using aptamers to elucidate esophageal cancer clinical samples
The epithelial cell adhesion molecule (EpCAM) is closely correlated with the occurrence and development of various cancers of epithelial origin. This study tested, for the first time, the ability of EpCAM aptamer SYL3C to detect EpCAM expression in 170 cases of esophageal cancer (EC) and precancerou...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685197/ https://www.ncbi.nlm.nih.gov/pubmed/26687301 http://dx.doi.org/10.1038/srep18516 |
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author | Liu, Zhenxu Lu, Yi Pu, Ying Liu, Jun Liu, Bo Yu, Bo Chen, Ke Fu, Ting Yang, Chaoyong James Liu, Huixia Tan, Weihong |
author_facet | Liu, Zhenxu Lu, Yi Pu, Ying Liu, Jun Liu, Bo Yu, Bo Chen, Ke Fu, Ting Yang, Chaoyong James Liu, Huixia Tan, Weihong |
author_sort | Liu, Zhenxu |
collection | PubMed |
description | The epithelial cell adhesion molecule (EpCAM) is closely correlated with the occurrence and development of various cancers of epithelial origin. This study tested, for the first time, the ability of EpCAM aptamer SYL3C to detect EpCAM expression in 170 cases of esophageal cancer (EC) and precancerous lesions, as well as 20 cases of EC series samples, using immunofluorescence imaging analysis. Corresponding antibodies were used as control. EpCAM overexpression was 98% in both esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EACA) and 100% in metastasis, but no EpCAM overexpression was detected in undifferentiated EC (UEC). Significant differences were noted among various stages of differentiation (p < 0.05) with the degree of differentiation inversely correlated with the expression of EpCAM. Overexpressed EpCAM was detected in severe dysplasia, but negative in mild to moderate dysplasia and benign esophageal lesions. In a competitive binding experiment, EpCAM aptamer generated a staining pattern similar to that of antibody, but the binding sites with EpCAM were different. Based on these results, it can be concluded that EpCAM is suitable for use as an EC biomarker, therapeutic target, and effective parameter for tumor transfer and prognosis evaluation by aptamer SYL3C staining. |
format | Online Article Text |
id | pubmed-4685197 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46851972015-12-30 Using aptamers to elucidate esophageal cancer clinical samples Liu, Zhenxu Lu, Yi Pu, Ying Liu, Jun Liu, Bo Yu, Bo Chen, Ke Fu, Ting Yang, Chaoyong James Liu, Huixia Tan, Weihong Sci Rep Article The epithelial cell adhesion molecule (EpCAM) is closely correlated with the occurrence and development of various cancers of epithelial origin. This study tested, for the first time, the ability of EpCAM aptamer SYL3C to detect EpCAM expression in 170 cases of esophageal cancer (EC) and precancerous lesions, as well as 20 cases of EC series samples, using immunofluorescence imaging analysis. Corresponding antibodies were used as control. EpCAM overexpression was 98% in both esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EACA) and 100% in metastasis, but no EpCAM overexpression was detected in undifferentiated EC (UEC). Significant differences were noted among various stages of differentiation (p < 0.05) with the degree of differentiation inversely correlated with the expression of EpCAM. Overexpressed EpCAM was detected in severe dysplasia, but negative in mild to moderate dysplasia and benign esophageal lesions. In a competitive binding experiment, EpCAM aptamer generated a staining pattern similar to that of antibody, but the binding sites with EpCAM were different. Based on these results, it can be concluded that EpCAM is suitable for use as an EC biomarker, therapeutic target, and effective parameter for tumor transfer and prognosis evaluation by aptamer SYL3C staining. Nature Publishing Group 2015-12-21 /pmc/articles/PMC4685197/ /pubmed/26687301 http://dx.doi.org/10.1038/srep18516 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Liu, Zhenxu Lu, Yi Pu, Ying Liu, Jun Liu, Bo Yu, Bo Chen, Ke Fu, Ting Yang, Chaoyong James Liu, Huixia Tan, Weihong Using aptamers to elucidate esophageal cancer clinical samples |
title | Using aptamers to elucidate esophageal cancer clinical samples |
title_full | Using aptamers to elucidate esophageal cancer clinical samples |
title_fullStr | Using aptamers to elucidate esophageal cancer clinical samples |
title_full_unstemmed | Using aptamers to elucidate esophageal cancer clinical samples |
title_short | Using aptamers to elucidate esophageal cancer clinical samples |
title_sort | using aptamers to elucidate esophageal cancer clinical samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4685197/ https://www.ncbi.nlm.nih.gov/pubmed/26687301 http://dx.doi.org/10.1038/srep18516 |
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