Cargando…

Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment

Circulating tumor cells (CTCs) have been considered as the origin of cancer metastasis. Thus, detection of CTCs in peripheral blood is of great value in different types of solid tumors. However, owing to extremely low abundance of CTCs, detection of them has been technically challenging. To establis...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Shuyi, Zhang, Chunxiao, Wang, Guozhou, Cheng, Boran, Wang, Yulei, Chen, Fangfang, Chen, Yuanyuan, Feng, Maohui, Xiong, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997243/
https://www.ncbi.nlm.nih.gov/pubmed/27570557
http://dx.doi.org/10.7150/thno.15284
_version_ 1782449735499513856
author Wang, Shuyi
Zhang, Chunxiao
Wang, Guozhou
Cheng, Boran
Wang, Yulei
Chen, Fangfang
Chen, Yuanyuan
Feng, Maohui
Xiong, Bin
author_facet Wang, Shuyi
Zhang, Chunxiao
Wang, Guozhou
Cheng, Boran
Wang, Yulei
Chen, Fangfang
Chen, Yuanyuan
Feng, Maohui
Xiong, Bin
author_sort Wang, Shuyi
collection PubMed
description Circulating tumor cells (CTCs) have been considered as the origin of cancer metastasis. Thus, detection of CTCs in peripheral blood is of great value in different types of solid tumors. However, owing to extremely low abundance of CTCs, detection of them has been technically challenging. To establish a simple and efficient method for CTCs detection in patients with hepatocellular carcinoma (HCC), we applied biocompatible and transparent HA/CTS (Hydroxyapatite/chitosan) nanofilm to achieve enhanced topographic interactions with nanoscale cellular surface components, and we used sLex-AP (aptamer for carbohydrate sialyl Lewis X) to coat onto HA/CTS nanofilm for efficient capture of HCC CTCs, these two functional components combined to form our CTC-(BioT)Chip platform. Using this platform, we realized HCC CTCs' capture and identification, the average recovery rate was 61.6% or more at each spiking level. Importantly, our platform identified CTCs (2±2 per 2 mL) in 25 of 42 (59.5%) HCC patients. Moreover, both the positivity rate and the number of detected CTCs were significantly correlated with tumor size, portal vein tumor thrombus, and the TNM (tumor-node-metastasis) stage. In summary, our CTC-(BioT)Chip platform provides a new method allowing for simple but efficient detection of CTCs in HCC patients, and it holds potential of clinically usefulness in monitoring HCC prognosis and guiding individualized treatment in the future.
format Online
Article
Text
id pubmed-4997243
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Ivyspring International Publisher
record_format MEDLINE/PubMed
spelling pubmed-49972432016-08-26 Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment Wang, Shuyi Zhang, Chunxiao Wang, Guozhou Cheng, Boran Wang, Yulei Chen, Fangfang Chen, Yuanyuan Feng, Maohui Xiong, Bin Theranostics Research Paper Circulating tumor cells (CTCs) have been considered as the origin of cancer metastasis. Thus, detection of CTCs in peripheral blood is of great value in different types of solid tumors. However, owing to extremely low abundance of CTCs, detection of them has been technically challenging. To establish a simple and efficient method for CTCs detection in patients with hepatocellular carcinoma (HCC), we applied biocompatible and transparent HA/CTS (Hydroxyapatite/chitosan) nanofilm to achieve enhanced topographic interactions with nanoscale cellular surface components, and we used sLex-AP (aptamer for carbohydrate sialyl Lewis X) to coat onto HA/CTS nanofilm for efficient capture of HCC CTCs, these two functional components combined to form our CTC-(BioT)Chip platform. Using this platform, we realized HCC CTCs' capture and identification, the average recovery rate was 61.6% or more at each spiking level. Importantly, our platform identified CTCs (2±2 per 2 mL) in 25 of 42 (59.5%) HCC patients. Moreover, both the positivity rate and the number of detected CTCs were significantly correlated with tumor size, portal vein tumor thrombus, and the TNM (tumor-node-metastasis) stage. In summary, our CTC-(BioT)Chip platform provides a new method allowing for simple but efficient detection of CTCs in HCC patients, and it holds potential of clinically usefulness in monitoring HCC prognosis and guiding individualized treatment in the future. Ivyspring International Publisher 2016-08-07 /pmc/articles/PMC4997243/ /pubmed/27570557 http://dx.doi.org/10.7150/thno.15284 Text en © 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
Wang, Shuyi
Zhang, Chunxiao
Wang, Guozhou
Cheng, Boran
Wang, Yulei
Chen, Fangfang
Chen, Yuanyuan
Feng, Maohui
Xiong, Bin
Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment
title Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment
title_full Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment
title_fullStr Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment
title_full_unstemmed Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment
title_short Aptamer-Mediated Transparent-Biocompatible Nanostructured Surfaces for Hepotocellular Circulating Tumor Cells Enrichment
title_sort aptamer-mediated transparent-biocompatible nanostructured surfaces for hepotocellular circulating tumor cells enrichment
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997243/
https://www.ncbi.nlm.nih.gov/pubmed/27570557
http://dx.doi.org/10.7150/thno.15284
work_keys_str_mv AT wangshuyi aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT zhangchunxiao aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT wangguozhou aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT chengboran aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT wangyulei aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT chenfangfang aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT chenyuanyuan aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT fengmaohui aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment
AT xiongbin aptamermediatedtransparentbiocompatiblenanostructuredsurfacesforhepotocellularcirculatingtumorcellsenrichment