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Using DNA Aptamer Probe for Immunostaining of Cancer Frozen Tissues
[Image: see text] Tissue immunostaining is critically important in clinical applications, and antibodies have been used extensively as the molecular probes. Recently, aptamer, as a new class of probes, have attracted much attention for their potential clinical and research value. Epithelial cell adh...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318623/ https://www.ncbi.nlm.nih.gov/pubmed/25536018 http://dx.doi.org/10.1021/ac504175h |
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author | Pu, Ying Liu, Zhenxu Lu, Yi Yuan, Peng Liu, Jun Yu, Bo Wang, Guodong Yang, Chaoyong James Liu, Huixia Tan, Weihong |
author_facet | Pu, Ying Liu, Zhenxu Lu, Yi Yuan, Peng Liu, Jun Yu, Bo Wang, Guodong Yang, Chaoyong James Liu, Huixia Tan, Weihong |
author_sort | Pu, Ying |
collection | PubMed |
description | [Image: see text] Tissue immunostaining is critically important in clinical applications, and antibodies have been used extensively as the molecular probes. Recently, aptamer, as a new class of probes, have attracted much attention for their potential clinical and research value. Epithelial cell adhesion molecule (EpCAM) is a specific biomarker which is overexpressed in many cancers of epithelial origin. Here, a DNA-based EpCAM aptamer SYL3C is reported as a probe for the immunostaining of frozen and paraffin-embedded sections of colorectal cancer tissues. Commercialized EpCAM antibodies were also used as a standard control. EpCAM aptamer SYL3C specifically recognized and immunostained cancer nests of colorectal tumor sections, but it neither reacted with background cells within tumor sites nor exhibited cross-reaction to the benign lesions or inflammation of colorectal tissues. No cross-linking to EpCAM-negative malignant tumor sections occurred. Compared with standard antibody staining, our EpCAM aptamer SYL3C protocol is simpler to implement with a shorter reaction time. Moreover, SYL3C can specifically bind with either frozen or paraffin-embedded tissue sections. Since the histopathology of frozen tissue is closer to that of fresh tissue and since frozen sections can be produced more quickly than paraffin-embedded sections, SYL3C immunostaining of frozen sections is a quick protocol that is easy to implement. |
format | Online Article Text |
id | pubmed-4318623 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-43186232015-12-23 Using DNA Aptamer Probe for Immunostaining of Cancer Frozen Tissues Pu, Ying Liu, Zhenxu Lu, Yi Yuan, Peng Liu, Jun Yu, Bo Wang, Guodong Yang, Chaoyong James Liu, Huixia Tan, Weihong Anal Chem [Image: see text] Tissue immunostaining is critically important in clinical applications, and antibodies have been used extensively as the molecular probes. Recently, aptamer, as a new class of probes, have attracted much attention for their potential clinical and research value. Epithelial cell adhesion molecule (EpCAM) is a specific biomarker which is overexpressed in many cancers of epithelial origin. Here, a DNA-based EpCAM aptamer SYL3C is reported as a probe for the immunostaining of frozen and paraffin-embedded sections of colorectal cancer tissues. Commercialized EpCAM antibodies were also used as a standard control. EpCAM aptamer SYL3C specifically recognized and immunostained cancer nests of colorectal tumor sections, but it neither reacted with background cells within tumor sites nor exhibited cross-reaction to the benign lesions or inflammation of colorectal tissues. No cross-linking to EpCAM-negative malignant tumor sections occurred. Compared with standard antibody staining, our EpCAM aptamer SYL3C protocol is simpler to implement with a shorter reaction time. Moreover, SYL3C can specifically bind with either frozen or paraffin-embedded tissue sections. Since the histopathology of frozen tissue is closer to that of fresh tissue and since frozen sections can be produced more quickly than paraffin-embedded sections, SYL3C immunostaining of frozen sections is a quick protocol that is easy to implement. American Chemical Society 2014-12-23 2015-02-03 /pmc/articles/PMC4318623/ /pubmed/25536018 http://dx.doi.org/10.1021/ac504175h Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Pu, Ying Liu, Zhenxu Lu, Yi Yuan, Peng Liu, Jun Yu, Bo Wang, Guodong Yang, Chaoyong James Liu, Huixia Tan, Weihong Using DNA Aptamer Probe for Immunostaining of Cancer Frozen Tissues |
title | Using DNA Aptamer Probe for Immunostaining of Cancer
Frozen Tissues |
title_full | Using DNA Aptamer Probe for Immunostaining of Cancer
Frozen Tissues |
title_fullStr | Using DNA Aptamer Probe for Immunostaining of Cancer
Frozen Tissues |
title_full_unstemmed | Using DNA Aptamer Probe for Immunostaining of Cancer
Frozen Tissues |
title_short | Using DNA Aptamer Probe for Immunostaining of Cancer
Frozen Tissues |
title_sort | using dna aptamer probe for immunostaining of cancer
frozen tissues |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4318623/ https://www.ncbi.nlm.nih.gov/pubmed/25536018 http://dx.doi.org/10.1021/ac504175h |
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