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Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer

BACKGROUND: In addition to conventional approaches, detecting and characterizing CTCs in patient blood allows for early diagnosis of cancer metastasis. METHODS: We blended poly(ethylene oxide) (PEO) into nylon-6 through electrospinning to generate a fibrous matbased circulating tumour cells (CTCs) a...

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Autores principales: Lee, Ai-Wei, Lin, Fu-Xiang, Wei, Po-Li, Jian-Wei, Guo, Chen, Jem-Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769517/
https://www.ncbi.nlm.nih.gov/pubmed/29338768
http://dx.doi.org/10.1186/s12951-017-0330-1
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author Lee, Ai-Wei
Lin, Fu-Xiang
Wei, Po-Li
Jian-Wei, Guo
Chen, Jem-Kun
author_facet Lee, Ai-Wei
Lin, Fu-Xiang
Wei, Po-Li
Jian-Wei, Guo
Chen, Jem-Kun
author_sort Lee, Ai-Wei
collection PubMed
description BACKGROUND: In addition to conventional approaches, detecting and characterizing CTCs in patient blood allows for early diagnosis of cancer metastasis. METHODS: We blended poly(ethylene oxide) (PEO) into nylon-6 through electrospinning to generate a fibrous matbased circulating tumour cells (CTCs) assay. The contents of nylon-6 and PEO in the electrospun blend fibrous mats (EBFMs) were optimized to facilitate high cell-substrate affinity and low leukocyte adsorption. RESULTS: Compared with the IsoFlux System, a commercial instrument for CTC detection, the CTC assay of EBFMs exhibited lower false positive readings and high sensitivity and selectivity with preclinical specimens. Furthermore, we examined the clinical diagnosis accuracy of colorectal cancer, using the CTC assay and compared the results with those identified through pathological analyses of biopsies from colonoscopies. Our positive expressions of colorectal cancer through CTC detection completely matched those recognized through the pathological analyses for the individuals having stage II, III, and IV colorectal cancer. Nevertheless, two in four individuals having stage I colorectal cancer, recognized through pathological analysis of biopsies from colonoscopies, exhibited positive expression of CTCs. Ten individuals were identified through pathological analysis as having no colorectal tumours. Nevertheless, two of these ten individuals exhibited positive expression of CTCs. CONCLUSIONS: Thus, in this population, the low cost EBFMs exhibited considerable capture efficiency for the non-invasive diagnosis of colorectal cancer.
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spelling pubmed-57695172018-01-25 Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer Lee, Ai-Wei Lin, Fu-Xiang Wei, Po-Li Jian-Wei, Guo Chen, Jem-Kun J Nanobiotechnology Research BACKGROUND: In addition to conventional approaches, detecting and characterizing CTCs in patient blood allows for early diagnosis of cancer metastasis. METHODS: We blended poly(ethylene oxide) (PEO) into nylon-6 through electrospinning to generate a fibrous matbased circulating tumour cells (CTCs) assay. The contents of nylon-6 and PEO in the electrospun blend fibrous mats (EBFMs) were optimized to facilitate high cell-substrate affinity and low leukocyte adsorption. RESULTS: Compared with the IsoFlux System, a commercial instrument for CTC detection, the CTC assay of EBFMs exhibited lower false positive readings and high sensitivity and selectivity with preclinical specimens. Furthermore, we examined the clinical diagnosis accuracy of colorectal cancer, using the CTC assay and compared the results with those identified through pathological analyses of biopsies from colonoscopies. Our positive expressions of colorectal cancer through CTC detection completely matched those recognized through the pathological analyses for the individuals having stage II, III, and IV colorectal cancer. Nevertheless, two in four individuals having stage I colorectal cancer, recognized through pathological analysis of biopsies from colonoscopies, exhibited positive expression of CTCs. Ten individuals were identified through pathological analysis as having no colorectal tumours. Nevertheless, two of these ten individuals exhibited positive expression of CTCs. CONCLUSIONS: Thus, in this population, the low cost EBFMs exhibited considerable capture efficiency for the non-invasive diagnosis of colorectal cancer. BioMed Central 2018-01-16 /pmc/articles/PMC5769517/ /pubmed/29338768 http://dx.doi.org/10.1186/s12951-017-0330-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Lee, Ai-Wei
Lin, Fu-Xiang
Wei, Po-Li
Jian-Wei, Guo
Chen, Jem-Kun
Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
title Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
title_full Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
title_fullStr Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
title_full_unstemmed Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
title_short Binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
title_sort binary-blend fibber-based capture assay of circulating tumor cells for clinical diagnosis of colorectal cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5769517/
https://www.ncbi.nlm.nih.gov/pubmed/29338768
http://dx.doi.org/10.1186/s12951-017-0330-1
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