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DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition

In this work, we have developed a truncated DNA aptamer, termed XQ-2d, with high affinity and specificity for pancreatic ductal adenocarcinoma (PDAC). Aptamer XQ-2d selectively binds to PL45 cells with a dissociation constant in the nanomolar range, as determined by its recognition of PL45 tumor cel...

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Autores principales: Wu, Xiaoqiu, Zhao, Zilong, Bai, Huarong, Fu, Ting, Yang, Chao, Hu, Xiaoxiao, Liu, Qiaoling, Champanhac, Carole, Teng, I-Ting, Ye, Mao, Tan, Weihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493536/
https://www.ncbi.nlm.nih.gov/pubmed/26155314
http://dx.doi.org/10.7150/thno.11938
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author Wu, Xiaoqiu
Zhao, Zilong
Bai, Huarong
Fu, Ting
Yang, Chao
Hu, Xiaoxiao
Liu, Qiaoling
Champanhac, Carole
Teng, I-Ting
Ye, Mao
Tan, Weihong
author_facet Wu, Xiaoqiu
Zhao, Zilong
Bai, Huarong
Fu, Ting
Yang, Chao
Hu, Xiaoxiao
Liu, Qiaoling
Champanhac, Carole
Teng, I-Ting
Ye, Mao
Tan, Weihong
author_sort Wu, Xiaoqiu
collection PubMed
description In this work, we have developed a truncated DNA aptamer, termed XQ-2d, with high affinity and specificity for pancreatic ductal adenocarcinoma (PDAC). Aptamer XQ-2d selectively binds to PL45 cells with a dissociation constant in the nanomolar range, as determined by its recognition of PL45 tumor cells in mice. Moreover, XQ-2d shows better recognition ratio for 40 tissue sections of clinical PDAC samples (82.5%) compared to the initial cell-SELEX selection library (5%). Therefore, XQ-2d can be considered a promising candidate as a tool for PDAC diagnosis and treatment.
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spelling pubmed-44935362015-07-07 DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition Wu, Xiaoqiu Zhao, Zilong Bai, Huarong Fu, Ting Yang, Chao Hu, Xiaoxiao Liu, Qiaoling Champanhac, Carole Teng, I-Ting Ye, Mao Tan, Weihong Theranostics Research Paper In this work, we have developed a truncated DNA aptamer, termed XQ-2d, with high affinity and specificity for pancreatic ductal adenocarcinoma (PDAC). Aptamer XQ-2d selectively binds to PL45 cells with a dissociation constant in the nanomolar range, as determined by its recognition of PL45 tumor cells in mice. Moreover, XQ-2d shows better recognition ratio for 40 tissue sections of clinical PDAC samples (82.5%) compared to the initial cell-SELEX selection library (5%). Therefore, XQ-2d can be considered a promising candidate as a tool for PDAC diagnosis and treatment. Ivyspring International Publisher 2015-06-06 /pmc/articles/PMC4493536/ /pubmed/26155314 http://dx.doi.org/10.7150/thno.11938 Text en © 2015 Ivyspring International Publisher. Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited. See http://ivyspring.com/terms for terms and conditions.
spellingShingle Research Paper
Wu, Xiaoqiu
Zhao, Zilong
Bai, Huarong
Fu, Ting
Yang, Chao
Hu, Xiaoxiao
Liu, Qiaoling
Champanhac, Carole
Teng, I-Ting
Ye, Mao
Tan, Weihong
DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition
title DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition
title_full DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition
title_fullStr DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition
title_full_unstemmed DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition
title_short DNA Aptamer Selected against Pancreatic Ductal Adenocarcinoma for in vivo Imaging and Clinical Tissue Recognition
title_sort dna aptamer selected against pancreatic ductal adenocarcinoma for in vivo imaging and clinical tissue recognition
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4493536/
https://www.ncbi.nlm.nih.gov/pubmed/26155314
http://dx.doi.org/10.7150/thno.11938
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