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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...

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Autores principales: Pu, Ying, Liu, Zhenxu, Lu, Yi, Yuan, Peng, Liu, Jun, Yu, Bo, Wang, Guodong, Yang, Chaoyong James, Liu, Huixia, Tan, Weihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
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.
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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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