Cargando…
Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging
Background: Capture and identification of circulating tumor cells (CTCs) in the blood system can help guide therapy and predict the prognosis of cancer patients. However, simultaneous capture and identification of CTCs with both epithelial and mesenchymal phenotypes remains a formidable technical ch...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4679383/ https://www.ncbi.nlm.nih.gov/pubmed/26722362 http://dx.doi.org/10.7150/jca.12722 |
_version_ | 1782405571900604416 |
---|---|
author | Chen, Yuan-Yuan Cheng, Bo-Ran He, Zhao-Bo Wang, Shu-Yi Wang, Zhen-Meng Sun, Min Song, Hai-Bin Fang, Yuan Chen, Fang-Fang Xiong, Bin |
author_facet | Chen, Yuan-Yuan Cheng, Bo-Ran He, Zhao-Bo Wang, Shu-Yi Wang, Zhen-Meng Sun, Min Song, Hai-Bin Fang, Yuan Chen, Fang-Fang Xiong, Bin |
author_sort | Chen, Yuan-Yuan |
collection | PubMed |
description | Background: Capture and identification of circulating tumor cells (CTCs) in the blood system can help guide therapy and predict the prognosis of cancer patients. However, simultaneous capture and identification of CTCs with both epithelial and mesenchymal phenotypes remains a formidable technical challenge for cancer research. This study aimed at developing a system to efficiently capture and identify these CTCs with heterogeneous phenotypes using transparent nanomaterials and quantum dots (QDs)-based multiplexed imaging. Methods: Hydroxyapatite-chitosan (HA-CTS) nanofilm-coated substrates were modified based on our previous work to increase the capture efficiency of cancer cell lines by extending baking and incubating time. QDs-based imaging was applied to detect cytokeratin, epithelial cell adhesion molecule (EpCAM), and vimentin of cancer cells to demonstrate the feasibility of multiplexed imaging. And QDs-based multiplexed imaging of CD45, cytokeratin and vimentin was applied to detect CTCs from different cancer patients that were captured using HA-CTS nanofilm substrates. Results: Comparisons of the capture efficiencies of cancer cells at different baking time of film formation and incubating time of cell capture revealed the optimal baking and incubating time. Optimal time was chosen to develop a modified CTCs capture system that could capture EpCAM-positive cancer cells at an efficiency > 80%, and EpCAM-negative cancer cells at an efficiency > 50%. QDs-based imaging exhibited comparable detection ability but higher photostability compared to organic dyes imaging in staining cells. In addition, QDs-based multiplexed imaging also showed the molecular profiles of cancer cell lines with different phenotypes well. The integrated CTCs capture and identification system successfully captured and imaged CTCs with different sub-phenotypes in blood samples from cancer patients. Conclusion: This study demonstrated a reliable capture and detection system for heterogeneous CTCs that combined enrichment equipment based on HA-CTS nanofilm substrates with QDs-based multiplexed imaging. |
format | Online Article Text |
id | pubmed-4679383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-46793832016-01-01 Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging Chen, Yuan-Yuan Cheng, Bo-Ran He, Zhao-Bo Wang, Shu-Yi Wang, Zhen-Meng Sun, Min Song, Hai-Bin Fang, Yuan Chen, Fang-Fang Xiong, Bin J Cancer Research Paper Background: Capture and identification of circulating tumor cells (CTCs) in the blood system can help guide therapy and predict the prognosis of cancer patients. However, simultaneous capture and identification of CTCs with both epithelial and mesenchymal phenotypes remains a formidable technical challenge for cancer research. This study aimed at developing a system to efficiently capture and identify these CTCs with heterogeneous phenotypes using transparent nanomaterials and quantum dots (QDs)-based multiplexed imaging. Methods: Hydroxyapatite-chitosan (HA-CTS) nanofilm-coated substrates were modified based on our previous work to increase the capture efficiency of cancer cell lines by extending baking and incubating time. QDs-based imaging was applied to detect cytokeratin, epithelial cell adhesion molecule (EpCAM), and vimentin of cancer cells to demonstrate the feasibility of multiplexed imaging. And QDs-based multiplexed imaging of CD45, cytokeratin and vimentin was applied to detect CTCs from different cancer patients that were captured using HA-CTS nanofilm substrates. Results: Comparisons of the capture efficiencies of cancer cells at different baking time of film formation and incubating time of cell capture revealed the optimal baking and incubating time. Optimal time was chosen to develop a modified CTCs capture system that could capture EpCAM-positive cancer cells at an efficiency > 80%, and EpCAM-negative cancer cells at an efficiency > 50%. QDs-based imaging exhibited comparable detection ability but higher photostability compared to organic dyes imaging in staining cells. In addition, QDs-based multiplexed imaging also showed the molecular profiles of cancer cell lines with different phenotypes well. The integrated CTCs capture and identification system successfully captured and imaged CTCs with different sub-phenotypes in blood samples from cancer patients. Conclusion: This study demonstrated a reliable capture and detection system for heterogeneous CTCs that combined enrichment equipment based on HA-CTS nanofilm substrates with QDs-based multiplexed imaging. Ivyspring International Publisher 2016-01-01 /pmc/articles/PMC4679383/ /pubmed/26722362 http://dx.doi.org/10.7150/jca.12722 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 Chen, Yuan-Yuan Cheng, Bo-Ran He, Zhao-Bo Wang, Shu-Yi Wang, Zhen-Meng Sun, Min Song, Hai-Bin Fang, Yuan Chen, Fang-Fang Xiong, Bin Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging |
title | Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging |
title_full | Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging |
title_fullStr | Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging |
title_full_unstemmed | Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging |
title_short | Capture and Identification of Heterogeneous Circulating Tumor Cells Using Transparent Nanomaterials and Quantum Dots-Based Multiplexed Imaging |
title_sort | capture and identification of heterogeneous circulating tumor cells using transparent nanomaterials and quantum dots-based multiplexed imaging |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4679383/ https://www.ncbi.nlm.nih.gov/pubmed/26722362 http://dx.doi.org/10.7150/jca.12722 |
work_keys_str_mv | AT chenyuanyuan captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT chengboran captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT hezhaobo captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT wangshuyi captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT wangzhenmeng captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT sunmin captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT songhaibin captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT fangyuan captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT chenfangfang captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging AT xiongbin captureandidentificationofheterogeneouscirculatingtumorcellsusingtransparentnanomaterialsandquantumdotsbasedmultiplexedimaging |