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Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()

Detecting the cancer cells in the peripheral blood, i.e. circulating tumor cell (CTC), have been considered as the “liquid biopsy” and become a particular area of focus. A deep insight into CTC provides a potential alternative method for early diagnosis of solid tumor. Previous studies showed that C...

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Detalles Bibliográficos
Autores principales: Cheng, Boran, Song, Haibin, Wang, Shuyi, Zhang, Chunxiao, Wu, Bibo, Chen, Yuanyuan, Chen, Fangfang, Xiong, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311046/
https://www.ncbi.nlm.nih.gov/pubmed/25500081
http://dx.doi.org/10.1016/j.tranon.2014.10.001
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author Cheng, Boran
Song, Haibin
Wang, Shuyi
Zhang, Chunxiao
Wu, Bibo
Chen, Yuanyuan
Chen, Fangfang
Xiong, Bin
author_facet Cheng, Boran
Song, Haibin
Wang, Shuyi
Zhang, Chunxiao
Wu, Bibo
Chen, Yuanyuan
Chen, Fangfang
Xiong, Bin
author_sort Cheng, Boran
collection PubMed
description Detecting the cancer cells in the peripheral blood, i.e. circulating tumor cell (CTC), have been considered as the “liquid biopsy” and become a particular area of focus. A deep insight into CTC provides a potential alternative method for early diagnosis of solid tumor. Previous studies showed that CTC counts could be regarded as an indicator in tumor diagnosis, predicting clinical outcomes and monitoring treatment responses. In this report, we utilize our facile and efficient CTC detection device made of hydroxyapatite/chitosan (HA/CTS) for rare cancer cells isolation and enumeration in clinical use. A biocompatible and surface roughness controllable nanofilm was deposited onto a glass slide to achieve enhanced topographic interactions with nanoscale cellular surface components, anti-EpCAM (epithelial cell adhesion molecule, EpCAM) were then coated onto the surface of nanosubstrate for specific capture of CTCs. This device performed a considerable and stable capture yields. We evaluated the relationship performance between serial CTC changes and the changes of tumor volume/serum tumor marker in gastrointestinal cancer patients undergoing anti-cancer treatments. The present study results showed that changes in the number of CTC were associated with tumor burden and progression. Enumeration of CTCs in cancer patients may predict clinical response. Longitudinal monitoring of individual patients during the therapeutic process showed a close correlation between CTC quantity and clinical response to anti-cancer therapy. Effectively capture of this device is capable of CTCs isolation and quantification for monitoring of cancer and predicting treatment response.
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spelling pubmed-43110462015-02-14 Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate() Cheng, Boran Song, Haibin Wang, Shuyi Zhang, Chunxiao Wu, Bibo Chen, Yuanyuan Chen, Fangfang Xiong, Bin Transl Oncol Article Detecting the cancer cells in the peripheral blood, i.e. circulating tumor cell (CTC), have been considered as the “liquid biopsy” and become a particular area of focus. A deep insight into CTC provides a potential alternative method for early diagnosis of solid tumor. Previous studies showed that CTC counts could be regarded as an indicator in tumor diagnosis, predicting clinical outcomes and monitoring treatment responses. In this report, we utilize our facile and efficient CTC detection device made of hydroxyapatite/chitosan (HA/CTS) for rare cancer cells isolation and enumeration in clinical use. A biocompatible and surface roughness controllable nanofilm was deposited onto a glass slide to achieve enhanced topographic interactions with nanoscale cellular surface components, anti-EpCAM (epithelial cell adhesion molecule, EpCAM) were then coated onto the surface of nanosubstrate for specific capture of CTCs. This device performed a considerable and stable capture yields. We evaluated the relationship performance between serial CTC changes and the changes of tumor volume/serum tumor marker in gastrointestinal cancer patients undergoing anti-cancer treatments. The present study results showed that changes in the number of CTC were associated with tumor burden and progression. Enumeration of CTCs in cancer patients may predict clinical response. Longitudinal monitoring of individual patients during the therapeutic process showed a close correlation between CTC quantity and clinical response to anti-cancer therapy. Effectively capture of this device is capable of CTCs isolation and quantification for monitoring of cancer and predicting treatment response. Neoplasia Press 2014-12-10 /pmc/articles/PMC4311046/ /pubmed/25500081 http://dx.doi.org/10.1016/j.tranon.2014.10.001 Text en © 2014 Neoplasia Press, Inc. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/3.0/).
spellingShingle Article
Cheng, Boran
Song, Haibin
Wang, Shuyi
Zhang, Chunxiao
Wu, Bibo
Chen, Yuanyuan
Chen, Fangfang
Xiong, Bin
Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()
title Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()
title_full Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()
title_fullStr Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()
title_full_unstemmed Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()
title_short Quantification of Rare Cancer Cells in Patients With Gastrointestinal Cancer by Nanostructured Substrate()
title_sort quantification of rare cancer cells in patients with gastrointestinal cancer by nanostructured substrate()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4311046/
https://www.ncbi.nlm.nih.gov/pubmed/25500081
http://dx.doi.org/10.1016/j.tranon.2014.10.001
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